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. Author manuscript; available in PMC: 2009 Feb 1.
Published in final edited form as: Patient Educ Couns. 2007 Nov 26;70(2):157–172. doi: 10.1016/j.pec.2007.10.004

Meta-Analysis of Patient Education Interventions to Increase Physical Activity among Chronically Ill Adults

Vicki S Conn 1,*, Adam R Hafdahl 2, Sharon A Brown 3, Lori M Brown 4
PMCID: PMC2324068  NIHMSID: NIHMS39529  PMID: 18023128

Abstract

Objective

This meta-analysis integrates primary research testing the effect of patient education to increase physical activity (PA) on behavior outcomes among adults with diverse chronic illnesses.

Methods

Extensive literature searching strategies located published and unpublished intervention studies that measured PA behavior outcomes. Primary study results were coded. Fixed- and random-effects meta-analytic procedures included moderator analyses.

Results

Data were synthesized across 22,527 subjects from 213 samples in 163 reports. The overall mean weighted effect size for two-group comparisons was 0.45 (higher mean for treatment than control). This effect size is consistent with a difference of 48 minutes of PA per week or 945 steps per day. Preliminary moderator analyses suggest interventions were most effective when they targeted only PA behavior, used behavioral strategies (vs. cognitive strategies), and encouraged PA self-monitoring. Differences among chronic illnesses were documented. Individual strategies unrelated to PA outcomes included supervised exercise sessions, exercise prescription, fitness testing, goal setting, contracting, problem solving, barriers management, and stimulus/cues. PA outcomes were unrelated to gender, age, ethnicity, or socioeconomic distribution among samples.

Conclusion

These findings suggest that some patient education interventions to increase PA are effective, despite considerable heterogeneity in the magnitude of intervention effect.

Practice Implications

Moderator analyses are preliminary and provide suggestive evidence for further testing of interventions to inform practice.

Keywords: patient education, exercise, meta-analysis, health behavior change

1. Introduction

Health care providers routinely recommend physical activity (PA) to many adults with chronic illnesses. Despite widespread recognition of potential health and well-being benefits of PA, most adults with chronic illnesses remain sedentary. Numerous primary studies have tested diverse patient education interventions to increase PA, and many authors have reviewed these investigations. Most reviews, including meta-analyses, have focused on benefits of PA. The many narrative reviews focused on PA behavior outcomes have examined limited domains of this broad literature, such as computer-tailored interventions [1]; primary care-based interventions [2-5]; environmental interventions [6,7]; mass media-delivered interventions [8]; interventions designed to increase ‘lifestyle’ PA (versus episodic exercise) [9,10]; interventions targeting older adults [11,12]; studies addressing subpopulations such as African-Americans [13-19]; and intervention studies based on particular theoretical models [20]. Narrative reviews discussing PA behavior outcomes often address very few of the available studies [21-24]. Narrative reviews often rely heavily on previous reviews [19], perhaps because it is difficult to conduct a narrative summary across many studies. Narrative reviews generally do not offer conclusions about the efficacy of interventions because evidence that appears contradictory is difficult to synthesize without quantitative integration [25,26]. This quantitative synthesis meets the current pressing need to integrate this large body of research to inform future research and facilitate behavior change theory development.

Few meta-analyses have examined PA outcomes following patient education interventions. Hillsdon, Foster, and Thorogood [27] synthesized across only 11 primary studies with healthy adults that reported PA outcomes. Conn et al. [11] synthesized intervention studies conducted with healthy and chronically ill aging adults. Ashworth, Chad, Harrison, Reeder, and Marshall [28] further limited their meta-analysis of studies conducted with older adults to comparisons between home- versus center-based interventions. Over a decade ago, Dishman and Buckworth [29] conducted the broadest meta-analysis across 127 studies of healthy and chronically ill adults and children. Fewer than 20% of the studies included in that study focused on persons with chronic illness. The authors reported that intervention effects sizes (ESs) were smaller among studies with chronically ill subjects than in studies with healthy subjects. In contrast, Conn et al. [11] reported that among studies of older adults, interventions targeting samples with specific chronic illnesses reported larger ESs than studies with diverse older adults. No comprehensive meta-analyses have been reported that address PA behavior following patient education interventions among adults with diverse chronic illnesses. This meta-analysis was designed to integrate primary study findings from interventions designed to increase PA behavior among adults with chronic illnesses.

This synthesis addressed the following questions (1) What are the overall effects of interventions to increase PA on PA behavior after interventions? (2) Do interventions' effects on PA behavior vary depending on characteristics of interventions, sample, or methodology? (3) For controlled trials, do control groups' post-test outcome measures different significantly from pre-test values?

2. Methods

We used standard quantitative review methods to identify and retrieve potential primary studies, determine study eligibility, reliably code data, synthesize results across primary studies, and interpret findings [30-35].

2.1 Inclusion Criteria

English-language reports of PA interventions among chronically ill subjects more than 18 years old were eligible for inclusion. We included studies with both an explicit intervention to increase PA and a measure of PA behavior following the intervention reported with adequate detail to calculate ESs. We included interventions broadly defined as patient education, that is planned activities which could include teaching, counseling, behavior modification, and exercise practice sessions which could influence subsequent PA behavior. We operationalized PA as any bodily movement that results in elevated energy expenditure beyond basal levels. Exercise, a subset of PA, was defined as structured, planned, and repetitive movement intended to increase fitness. A few studies addressed the broader construct of PA, though most targeted exercise.

Both published and unpublished studies were included. Meta-analyses that only include published studies are likely to overestimate the overall ES because the most consistent difference between published and unpublished studies is the statistical significance of the findings [36]. Small-sample studies were included to synthesize across the broad scope of investigations. Although these studies may lack statistical power, they can contribute important information from difficult-to-recruit subjects or innovative interventions [37]. We weighted studies so that smaller studies had proportionally less impact on aggregate findings. Pre-experimental studies with pre-intervention and post-intervention data to calculate ESs were included because some investigators find it unethical to withhold potentially beneficial treatments, and because novel interventions may be tested initially in these designs [38,39]. These pre-experimental studies were analyzed separately from two group comparisons. We were able to include a broader variety of studies by including studies with multiple designs.

2.2 Search Strategies

We used multiple search strategies to ensure a comprehensive search and widen the scope of studies beyond those identified in previously published reviews [36]. The broad searching was an important technique to avoid the bias resulting from narrow searches [37]. An experienced reference librarian conducted searches in MEDLINE, PsycINFO, EMBASE, CINAHL, Cochrane Controlled Trials Register, Database of Abstracts of Reviews of Effectiveness, Healthstar, Combined Health Information Database, Sport Discus, Dissertation Abstracts International, and Educational Resources Information Center. We searched the National Institutes of Health Computer Retrieval of Information on Scientific Projects (CRISP) data of funded studies back to 1973. To ensure comprehensive searches of computerized databases, we employed broad search terms for intervention (adherence, behavior therapy, clinical trial, compliance, counseling, evaluation, evaluation study, evidence-based medicine, health care evaluation, health behavior, health education, health promotion, intervention, outcome & process assessment, patient education, program, program development, program evaluation, self care, treatment outcome, validation study) and PA (exercise, physical activity, physical fitness, exertion, exercise therapy, physical education & training, walking). Computerized author database searches were conducted on principal investigators of funded studies and all authors of eligible studies. Senior authors of eligible studies were contacted to solicit additional papers. Ancestry searches were conducted on all eligible studies and previous reviews. We conducted hand searches for articles from 1970 (or initial year of publication) through 2004 in 215 journals where eligible studies were published, review papers were retrieved, or research team members suggested primary studies might be published. Internet searches were conducted but did not yield any primary studies not located through other mechanisms.

2.3 Data Coding

We developed, pilot tested, and refined a coding frame to record results of primary studies and characteristics of sources, study participants, study methods, and interventions. Source characteristics include presence of funding, dissemination vehicle, and year of distribution. Gender, minority, age, socio-economic status, and medical diagnoses were coded to describe subjects. Interventions could include motivational/educational sessions and/or supervised exercise sessions. Because supervised exercise sessions are a common health behavior change intervention with chronically ill adults, details of supervised exercise sessions were coded as available in study reports (intensity, duration, frequency per week, weeks of supervised exercise). Coded intervention attributes include intervention social context (group vs. individual), weeks over which the intervention was delivered, behavioral target (PA only vs. multiple health behaviors including PA), recommended duration of exercise sessions, recommended exercise frequency per week, recommended form of exercise, and several intervention content attributes (Table 1). We coded data at a micro-level with very specific details to enhance coder reliability. Coding specific details was appropriate because universal definitions of broad categories of interventions (e.g. self-management) are not available. We recorded PA behavior only if the PA measure clearly was separated from any intervention supervised exercise sessions (e.g. cardiac rehabilitation participation). The most distal data collection point was used to calculate ESs since enduring PA behavior changes will most likely lead to health benefits. To establish reliability, two extensively trained coders independently extracted all data. The senior author or other member of the research team resolved any coding discrepancies.

Table 1. Intervention Content Reported by More than 10 of the Studies*.

Characteristic Description Frequency
Supervised exercise Provision of supervised exercise sessions at a specified location. 88
Self-monitoring Subjects record physical activity (PA) behavior. Includes activity diaries. 66
Exercise prescription Individualized specific form, intensity, frequency and/or duration of exercise suggested to each subject. May include prescription for progression of exercise. 65
Fitness testing Testing subjects' physical fitness when the testing was intended to change behavior. Not coded when fitness testing measured outcomes but information was not provided to subjects as a strategy to change behavior. 57
Goal setting Subjects generate written or oral behavioral change goals. 55
Problem-solving Teaching subject problem-solving strategies or conducting problem-solving activities (name problems, generate potential solutions specific to exercise behavior, decide on a course of action, and evaluate effects of solution implemented) during sessions with the investigator. 50
Feedback Explicit information provided to subjects about their performance. Could include a comparison with a group norm or standard or with subjects' own past behavior. 43
Social modeling Opportunities to watch similar others exercise. 40
Barriers management Teaching subjects to overcome or manage barriers (obstacles, deterrents). Could include having subjects identify barriers and brainstorm strategies to overcome them or could be teaching methods to overcome barriers that researchers identify. 39
Monitoring Research staff monitors subjects' physical activity performance. 39
Social support Deliberate building of social relationships to foster increased physical activity (e.g. self-help groups, ‘social support’). Includes team building but not team competition for rewards. 35
Modeling Opportunities to watch others exercise who may not be similar to subjects. 33
Consequences Specific planned tangible or intangible positive consequences of behavior change (e.g. lottery for prizes, praise, token economy, competition that has a reward, contracting for a reward, social reinforcement) when the research team or subject administers the reward. 28
Contracting Written agreements including specific behavior change in stated time frame. 16
Symptom monitoring/management Subjects taught to monitor PA-related symptoms and modify PA to manage symptoms. Not coded when subjects were taught which symptoms would prompt cessation of PA for safety. 16
Health risk appraisal Specific researcher-provided algorithm of quantifiable risks of major illness that can be altered by PA behavior. 14
Relapse prevention education Specific program to prepare subjects for lapse, relapse, slip, backsliding, failures, abstinence violation effect. Only coded when report used the phrase relapse prevention education. 14
Stimulus control Object of event that stimulates PA behavior (e.g. cues, prompts, telephone calls, reminders located strategically). 14
*

Studies could report multiple intervention strategies.

2.4 Data Management and Analyses

We used standard meta-analytic approaches for data calculations. We calculated a standardized mean difference (d) as each comparison's ES. More favorable outcome scores for treatment groups or at post-test are reflected in a positive d. We analyzed single treatment group pre- and post-intervention ESs separately from two-group ESs, but expressed both types of ESs in the raw-score metric to facilitate comparisons. Although both random- and fixed-effects analyses were conducted, we present only random-effects analyses. See Table 2 for details of statistical analyses.

Table 2. Statistical Management of Data.

Analysis component Approach or rationale
Standardized mean difference [33,34,49] Post-intervention difference between treatment and control group divided by the pooled SD, for two-group comparisons.
Difference between pre- and post-test scores divided by pre-intervention SD for single-group comparisons, under assumptions of no (ρ12 = 0.0) and high association (ρ12 = 0.80) between pre- and post-scores; calculated for all pre-post treatment and control groups with adequate data.
Adjusted for small sample bias.
Weighted by inverse of variance to address sample size differences.
95% confidence intervals for mean ES constructed from normal-theory stand errors.
Studies with multiple treatment groups without a control group were treated as single-group studies.
Dependencies in data for few studies with one control group and two or three treatment groups Each study's dependent ESs combined in a single independent ES by generalized least-squares approach and then treated as standard univariate random-effects analyses. [50]
Outlier determination ESs examined graphically.
Externally standardized residuals evaluated as removed each ES one at a time.
Homogeneity analyses after omitting each case in turn.
Publication bias determination [51] ES plotted against sampling variance.
Examined for funnel-shaped plot indicating symmetrical distribution around estimated population mean ES.
Homogeneity Q calculated from weighted sum of squares (chi-squared distribution).
Random-effects model Assumes individual ESs vary due to both subject-level sampling error and other sources of study-level error such as variations among interventions.
Consistent with heterogeneous study implementation.
Weighted method of moments used to estimate between studies variance component.
Common Language Effect Size (CLES) [52] Probability that a random treatment subject would score higher than a random control subject (an ES of d = 0.0 corresponds to a CLES of 0.50).
Conversion to original metric [47] ES converted to original metric for variables with multiple studies reporting identical measures.
Reported for minutes of PA per week and for steps per day.
Moderator analysis [53,54] Mixed- and fixed-effects calculated, fixed-effects available from senior author.
Continuous moderators: effects tested by unstandardized regression slope ( β^) in meta-analytic analogue of regression.
Dichotomous moderators: effects tested by between-group heterogeneity statistic (Qbetween) using meta-analytic analogue of ANOVA.
Interpret findings cautiously when significant heterogeneity exists, large variance components decrease statistical power.
Multiple-df moderator analysis Categorical moderator with more than two levels or two dichotomous moderators in factorial design.
Multicategory moderator: Omnibus test of heterogeneity among levels (Qbetween) followed by focus contrasts among particular levels.
Two dichotomous moderators: Omnibus test comparing mean ES among four cells (Qbetween), tests of each main effect and interaction, and contrasts comparing particular cells (e.g., simple main effects).

Between-study ES homogeneity was assessed using a conventional heterogeneity statistic (Q). Heterogeneity was expected because it is very common among studies of educational and behavior interventions and in studies with diverse methodologies [40]. Recent Cochrane reviews of behavioral interventions have accepted heterogeneity and reported management strategies consistent with our approach [40-43]. We emphasize the random-effects analyses because it is a heterogeneous model that takes into account heterogeneity not fully explained by moderators. The random-effects analyses present a location parameter (mean ES) and quantify residual heterogeneity in a variance component [44]. We explored potential study-level moderators to understand potential sources of heterogeneity [41,44-48]. Finally, we interpreted our findings in the context of heterogeneity discovered. Interpreting the extent to which heterogeneity affects conclusions is more valuable than merely testing for the presence of heterogeneity [45]. Interested readers may consult Conn, Hafdahl, Mehr, LeMaster, Brown, and Nielsen [30] for a more detailed rationale for synthesizing across heterogeneous studies.

We conducted exploratory moderator analyses for two-group comparisons. Moderators were selected based on availability in primary reports and our ability to reliably code the attribute. We could not analyze many of the intriguing potential moderators because primary studies reported them infrequently. For example, we could not effectively analyze the impact of interventions based on social cognitive theory because reports provide too little information about conceptual frameworks and papers that claim to be based on particular theories often provide little evidence that the intervention is consistent with the theory. We grouped interventions into behavior and cognitive categories but did not make other groupings, such as self-management training, because universal definitions are not available and studies often provide insufficient information to accurately categorize studies. Because little previous research has provided a foundation for confirmatory hypothesis testing, the moderator analyses are intended as a hypothesis-generating contribution.

3. Results

A total of 213 samples including 22,557 subjects from 163 reports were eligible for the meta-analysis (numbers of subjects should be considered close approximations, given vagaries of primary-study reporting) [55-217]. We calculated independent groups ESs for 17,147 subjects in 129 samples from 105 reports. Pre-post treatment group comparisons were calculated for 146 samples, which included 9,275 subjects from 107 reports. A total of 3,218 subjects from 59 samples reported in 56 papers were included in the pre-post analysis of control subjects. Most reports were published articles, though some dissertations or theses (s=18) were included as well as a few presentation reports (s=4) and one book chapter (s=number reports, k=number comparisons). Most reported on studies with financial support (s=111). Only 21 reports appeared before 1990, and 73 were disseminated in 2000 or more recently.

Studies recruited samples with diverse chronic illnesses: mixed medically and surgically managed cardiac diseases (s=22), hypertension (s=10), peripheral vascular disease (s=11), myocardial infarction (s=10), coronary artery disease (s=12), coronary artery bypass graft (s=6), heart failure (s=6), mixed medically managed cardiac diseases (s=2), coronary angioplasty (s=1), type 2 diabetes (s=22), type 1 diabetes (s=6), mixed diabetes subjects (s=4), rheumatoid arthritis (s=9), osteoarthritis (s=8), heterogeneous arthritis (s=9), osteoporosis (s=5), breast cancer (s=4), gastrointestinal cancer (s=1), renal disease (s=2), chronic obstructive pulmonary disease (s=2), Parkinson's disease (s=1), multiple sclerosis (s=1), fibromyalgia (s=1), chronic fatigue syndrome (s=1), chronic back problems (s=1), mixed unspecific musculoskeletal diseases (s=1), hypopituitarism (s=1), and mixed chronic illnesses (s=15). Although not well reported, many studies did not exclude subjects with the co-morbidities commonly associated with the chronic illness target population. Further details about subjects with diabetes, cancer, arthritis, and cardiac disease are available in previous publications reporting on health outcomes among these studies [30,31,35,218-220].

Plots depicting ESs of PA versus sampling variance suggested the absence of studies with low or negative ESs for treatment group versus control group comparisons and for treatment group pre-post comparisons. Although this is consistent with a publication bias against non-significant or negative results, it may also arise from phenomena such as certain patterns of heterogeneity [221]. There was no evidence of publication bias for comparison group pre-post ES plots.

3.1 Primary study characteristics

Descriptive statistics for primary study characteristics are displayed in Table 3. Sample size varied extensively from 4 to 1173 subjects, with a median of 62 subjects. The median value for mean age was 59 years. Typically, almost half of the subjects were women, among studies that reported gender distribution. Minority inclusion was often not reported: 33 reports indicated including African Americans, 10 included Hispanics, and 2 included Native Americans. Only four papers reported on predominantly (50% or more) African-American subjects, only one on predominantly Hispanic subjects, and none on predominantly Native-American subjects. A few studies experienced significant attrition, though losses were typically modest and were similar between treatment and control groups.

Table 3. Characteristics of Primary Studies Included in Combined-Illness Physical Activity Meta-Analyses.

Characteristic k Min Q1 Mdn Q3 Max
Mean age (years) 156 22 54 59 65 82
Sample size per study 163 4 33 62 153 1173
Proportion of sample assigned to treatmenta 109 .25 .50 .51 .58 .79
Proportion attrition from treatment group 133 .00 .04 .11 .21 .52
Proportion attrition from comparison groupa 87 .00 .03 .11 .22 .59
Proportion female 140 .00 .25 .49 .79 1.00
Minutes of supervised exercise per session 51 10 40 60 60 300
Total number of supervised exercise sessions 60 4 17 36 38 202
Number of weeks intervention was delivered 143 1 6 12 24 208

Note. Includes all studies that contributed at least one independent-groups or pre-post effect size to primary analyses. Independent samples within studies aggregated by summing sample sizes before computing proportions and using weighted mean of other characteristics (weighted by sample size). k = number of studies providing data on characteristic; Q1 = first quartile, Q3 = third quartile.

a

Computed for independent-groups studies only.

Tables 1 and 3 include intervention attributes. Supervised exercise was the most common PA behavior change strategy among the studies (s=88). Typical attributes among studies with supervised exercise included 2 weekly 60-minute sessions over 12 weeks. Fifty-four studies included some form of mediated motivational or educational intervention delivery (e.g. telephone, mail, Internet), and 13 used only mediated intervention delivery. Several studies asked subjects to monitor their PA behavior (s=66) as a strategy to increase PA. Fitness testing (s=57) and individualized exercise prescription (s=65) were common intervention components. Modeling, either by research staff members (s=33) or by people similar to subjects (s=40), was very common. Many studies asked subjects to generate specific PA behavioral goals (s=55) in an effort to change behavior. Fifty studies either taught problem-solving skills to subjects or included problem solving during contacts with the research staff. Monitoring of PA behavior by research staff was also common (s=39). Forty-three studies provided explicit feedback to subjects about their PA behavior. Twenty-eight studies either provided rewards for subjects for increasing PA or taught subjects to reward themselves for PA. Thirty-five studies attempted to increase social support for PA. Thirty-nine studies specifically dealt with barriers to PA as a strategy to increase activity. Strategies less frequently reported include stimulus/cues to PA (s=14), relapse prevention education (s=14), health risk appraisal (s=14), symptom monitoring and management (s=16), and contracting (s=16). Intervention content reported by 10 or fewer studies included decision making (s=9), commitment activities (s=8), thought restructuring (s=7), values clarification (s=7), exercise variation (s=5), cognitive modification (s=4), decisional balance (s=3), personal trainer (s=2), shaping (s=2), community development (s=1), emotional arousal (s=1), imagery (s=1), and motivational interviewing (s=1). Most studies delivered the same interventions to all subjects, only six interventions were individually tailored (intervention content to motivate PA behavior change individually modified in systematic manner), and only two were targeted (different interventions for subsets of samples).

3.2 Effect of Patient Education Interventions on PA Outcomes

Table 4 presents the overall effects of interventions. The overall mean effect in two-group studies was 0.45. The treatment group pre- vs. post-test mean ESs were 0.41 (ρ12=0.80) and 0.51 (ρ12=0.00). The treatment group versus control group comparison and both treatment group pre- vs. post-test comparisons demonstrated significant ES heterogeneity according to the homogeneity test (Q in table 3). These findings document that although intervention effects were highly variable, interventions resulted in improved PA behavior scores on average. In contrast, control subjects generally experienced no improvement, with ES estimates of 0 that yielded 95% confidence intervals between -0.07 and 0.07.

Table 4. Random-Effects Physical Activity Behavior Outcome Estimates and Tests.

ES type k Q μ^δ SE(μ^δ) μδ 95%CI σ^δ
Independent-groupsa 129 444.08*** .46*** .035 (.39,.52) .301
Independent-groupsb 129 440.73*** .45*** .037 (.38,.52) .300
Treatment pre-post, ρ12 = .80 146 2058.55*** .41*** .029 (.35,.47) .325
Treatment pre-post, ρ12 = .00 160 820.84*** .51*** .038 (.43,.58) .389
Comparison pre-post, ρ12 = .80 59 463.49*** -.00 .035 (-.07,.07) .235
Comparison pre-post, ρ12 = .00 56 54.67 .00 .026 (-.05,.06) 0

Note. Under homogeneity Q is distributed approximately as chi-square with df = k − 1, where k is the number of (possibly dependent) observed effect sizes; this tests both homogeneity (H0: δ = δi) and the between-studies variance component σδ2(H0:σδ2=0). Weighted method of moments used to estimate σδ2. Potential outliers excluded based on random-effects standardized residuals.

a

Dependence due to 11 multiple-treatment pairs and 4 multiple-treatment triplets not accommodated.

b

Multiple-treatment dependence accommodated.

p < .10.

*

p < .05.

**

p < .01.

***

p < .001 (for , μ^δ, and Q).

To enhance interpretability, mean ESs were transformed to minutes of PA per week and steps per day, using results from appropriate reference groups pooled across available studies. The mean effect in terms of the pooled treatment and control SD (106.7) is a raw mean difference of 48.0 (0.45 × 106.7) PA minutes per week. Relative to the pooled post-test mean of 116.4 minutes for control subjects, this translates to a mean of 164.4 minutes of PA per week among treatment subjects. For single-group pre-post comparisons, the minutes per week raw mean difference is 38.4 minutes (ρ12=0.80 assumption); relative to the pooled mean baseline of 92.5 minutes per week this translates into mean outcome 130.9 minutes per week. For steps per day, the mean effect in terms of the pooled treatment and control SD (2101) is a steps-per-day raw mean difference of 945 (2101 × .45). Relative to the pooled post-test mean of 6108 steps for control subjects, this translates to a mean of 7053 steps per day among treatment subjects for the two-group comparison. For single-group pre-post comparisons, the steps per day raw mean difference is 870 steps (ρ12=0.80 assumption); relative to the pooled mean baseline of 4254 steps this translates into mean outcome 5124 steps per day. The CLES for the two-group comparisons was 0.62, indicating that 62% of the time, a random treatment subject would have higher PA scores than a random control subject. For single-group comparisons the random-effects estimates would be translated to CLES of .64 and .74 for assumptions of a low and high pre-post association, respectively. The CLES for control subjects was .50 indicating these subjects were no more likely to have higher PA scores after interventions than before interventions.

3.3 Moderator Analyses

The results from the dichotomous and continuous moderator analyses for two-group comparisons are presented in Tables 5 and 6. Studies reported more recently yielded slightly smaller ESs than studies distributed earlier (β^1=-.009). Studies published in journals did not report significantly different ESs as compared to unpublished studies. Studies with funding reported significantly lower ESs (.41) than studies without funding (.60). Gender distribution, ethnic minority proportion, sample age, and socioeconomic characteristics of samples were unrelated to ESs. Neither random assignment of subjects, attrition, nor the length of the follow-up period between intervention completion and PA outcome measurement were related to ESs.

Table 5. Independent-Groups Post-test Comparisons: Dichotomous Moderator Analyses.

Moderator Coded values k0 k1 μ^δ0 μ^δ1 QB QW σ^δ
Publication status 0 = unpublished,
1 = published
15 114 .44*** .46*** 0.0 443.8*** .302
Funding 0 = no funding,
1 = funding
35 94 .60*** .41*** 5.1* 399.0*** .283
SES 0 = low,
1 = moderate or high
4 6 .37 .27 0.1 25.7** .314
Random allocation 0 = absent,
1 = present
23 106 .58*** .43*** 2.6 440.1*** .301
Behavioral target 0 = physical activity only,
1 = multiple health behaviors
55 74 .57*** .38*** 7.4** 426.8*** .295
Supervised exercise 0 = absent,
1 = present
79 50 .41*** .53*** 2.5 441.0*** .302
Tailoring 0 = absent,
1 = present
125 4 .45*** .66*** 1.2 418.8*** .295
Mediated delivery 0 = face-to-face only,
1 = mail/telephone/mass media
97 32 .47*** .41*** 0.6 443.1*** .304
Intervention social context 0 = individual,
1 = group
43 85 .48*** .45*** 0.1 439.6*** .303
Social cognitive theory 0 = absent,
1 = present
97 32 .45*** .46*** 0.0 439.9*** .303
Transtheoretical model 0 = absent,
1 = present
117 12 .48*** .22* 4.7* 427.8*** .295
Behavioral–any 0 = no behavioral strategy,
1 = at least 1 behavioral strategy
30 99 .28*** .51*** 8.8** 412.7*** .289
Behavioral–pure 0 = cognitive or no behavioral,
1 = behavioral and no cognitivea
72 57 .40*** .53*** 3.1 438.0*** .301
Cognitive–any 0 = no cognitive strategy,
1 = at least 1 cognitive strategy
81 48 .46*** .44*** 0.1 442.0*** .303
Cognitive–pure 0 = behavioral or no cognitive,
1 = cognitive and no behavioralb
123 6 .47*** .10 5.6 437.8*** .302
Barriers management 0 = absent,
1 = present
101 28 .45*** .46*** 0.0 441.7*** .303
Consequences 0 = absent,
1 = present
111 18 .45*** .49*** 0.2 430.4*** .299
Contracting 0 = absent,
1 = present
118 11 .44*** .60*** 1.6 440.2*** .303
Exercise prescription 0 = absent,
1 = present
90 39 .42*** .53*** 2.1 438.8*** .301
Feedback 0 = absent,
1 = present
99 30 .47*** .42*** 0.4 442.4*** .304
Fitness testing 0 = absent,
1 = present
97 32 .43*** .55*** 1.8 444.0*** .303
Goal setting 0 = absent,
1 = present
92 37 .47*** .43*** 0.2 443.8*** .305
Problem solving 0 = absent,
1 = present
98 31 .44*** .50*** 0.5 436.3*** .301
Self-monitoring 0 = absent,
1 = present
87 42 .40*** .56*** 5.1* 397.1*** .281
Stimulus/cues 0 = absent,
1 = present
121 8 .45*** .56*** 0.5 442.2*** .301
Recommended specific exer. form 0 = other than walking,
1 = walking
115 14 .46*** .45*** 0.0 442.8*** .302
Recommended intensity 0 = low,
1 = moderate or high
5 40 .39 .60*** 0.9 142.5*** .396
Days after intervention 0 = none,
1 = at least one
43 80 .45*** .46*** 0.0 435.6*** .314

Note. kj = number of (possibly dependent) ES estimates in group coded j. Heterogeneity statistics: QB = between groups (distributed as chi-square on df = 1 under H0: μδ0 = μδ1), QW = combined within groups (distributed as chi-square on df = k0 + k1 − 2 under H0: σδ02=σδ12=0). Weighted method of moments used to estimate between-studies variance component σδ2. Analysis reported if k0 ≥3 and k1 ≥3.

p < .10.

*

p < .05.

**

p < .01.

***

p < .001 (for μ^δ0,μ^δ1, QB and QW).

a

0=no behavioral strategy or at least 1 cognitive strategy, 1=at least 1 behavioral strategy and no cognitive strategy.

b

0=no cognitive strategy or at least 1 behavioral strategy, 1=at least 1 cognitive strategy and no behavioral strategy.

Table 6. Linear Continuous Mixed-Effects Moderator Analyses for Physical Activity.

Moderator k Qresidual β^0 β^1 SE(β^1) σ^δ
Publication year 129 430.2*** 0.685 -0.009 0.0056 .297
Mean age 125 425.9*** 0.198 0.004 0.0040 .305
Proportion female 115 367.3*** 0.384 0.162 0.1225 .304
Proportion ethnic minority 24 47.7** 0.427 -0.317 0.2951 .312
Attrition proportion 92 328.0*** 0.467 -0.157 0.3865 .310
Days after intervention 80 291.8*** 0.757 -0.133 0.0969 .308
Number behavioral strategies 129 425.6*** 0.407 0.031 0.0232 .296
Number cognitive strategies 129 438.5*** 0.451 0.005 0.0310 .302
Number strategies 129 436.7*** 0.437 0.004 0.0094 .301
Sup. cont.–log10(min) 34 78.2*** -0.342 0.286 0.1835 .348
Mot. cont.–log10(min) 43 132.0*** 0.204 0.087 0.0995 .253
Recom. min/wk 34 114.7*** 0.142 0.003 0.0021 .409
Weeks of intervention 115 421.4*** 0.420 0.057 0.0646 .310

Note. k = number of (possibly dependent) ES estimates. Moderators: publication year (year – 1972); mean age (years); Pr. ethnic minority (proportion Black, Hispanic, or Native American); days after intervention (common log of days); number of strategies (number of coded strategies used in intervention, including behavioral, cognitive, and others); supervised contact–log10(min) (common log of positive minutes of supervised contact); motivational contact–log10(min) (common log of positive minutes of motivational/educational contact); weeks of intervention (common log of weeks of intervention). β^0 = unstandardized intercept estimate for uncentered moderator; β^1 = unstandardized slope estimate. Qresidual = residual heterogeneity statistic, beyond that due to moderator (distributed as chi-square on df = k − 2 under H0: σδ|x2=0, where x is moderator value). Weighted method of moments used to estimate between-studies variance component σδ2. Analysis reported if k ≥ 6.

p < .10.

*

p < .05.

**

p < .01.

***

p < .001 (for β^1 and Qresidual).

Interventions that targeted only PA behavior (.57) reported larger ESs than those attempting to change multiple behaviors such as PA and diet (.38). Interventions with supervised exercise sessions were no more effective in changing PA than those that relied exclusively on educational or motivational sessions. Individually tailored interventions were not associated with larger ES than more traditional interventions where all subjects receive the same content. The presence of mediated delivery (e.g. telephone, mail) was unrelated to ESs. Interventions were similarly effective regardless of whether they were delivered to individuals or groups.

Interventions based on social cognitive theory, the most commonly reported conceptual foundation for interventions, were unrelated to ESs. Studies of interventions based on the transtheoretical model reported significantly smaller ESs (.22) than studies that did not use this framework (.48). Studies that used any behavioral strategy (e.g. consequences, contracting, feedback, goal setting, self-monitoring, stimulus/cues, personal trainer) to increase PA reported larger ESs (.51) than studies that did not use any behavioral strategies. Studies that used exclusively behavioral strategies (.53) reported larger ESs than studies that did not consist entirely of behavioral intervention (.40). In contrast, the presence or absence of cognitive strategies (barriers management, decisional balance, motivational counseling, problem solving, social cognitive theory) was not associated with ESs. The difference between studies using only cognitive strategies (.10) versus those using cognitive strategies plus other strategies (.47) did not achieve statistical significance. Neither the number of cognitive strategies nor the number of behavioral strategies in interventions was related to ESs. Studies that directed subjects to self-monitor their PA behavior reported significantly larger ESs (.56) than studies that did not promote self-monitoring (.40). Other intervention content potential moderators were unrelated to ESs: barriers management, consequences, contracting, exercise prescription, feedback, fitness testing, goal setting, problem solving, and stimulus/cues. The number of strategies in the intervention did not predict ESs. Neither the weeks over which the intervention was delivered nor the amount of contact time between intervention staff and subject were related to the ESs of PA. The nature of the PA recommended to subjects (specific forms, intensities, minutes/week) was unrelated to PA behavior outcomes. Contact the senior author for information about associations among moderators and moderator analyses of treatment group pre-post comparisons.

The moderators reported above and in Tables 5 and 6 all involve single-df moderator effects. Multiple-df moderator analyses were conducted on a few moderator variables for independent group ESs. This entailed testing either one moderator with more than two levels or two dichotomous moderators, the latter of which permits examining moderator interactions. The ESs of PA differed significantly by type of chronic illness (Qbetween=9.1). The largest ES was for arthritis (.61), followed by diabetes (.49) and cardiac (.40). The smallest ES was among studies of cancer patients (-.03). The single moderator analyses we report for behavioral and cognitive strategies was supported in a multiple moderator analyses (Qbetween=10.5). The analyses found the largest ES for studies with only behavioral strategies (.53) followed by studies with both behavioral and cognitive intervention (.50). ESs were smallest among studies with cognitive strategies and no behavioral intervention (.10).

4. Discussion and Conclusion

4.1 Discussion

This is the first meta-analysis to examine PA behavior following patient education interventions designed to increase PA among diverse chronically ill populations. Our extensive search strategies successfully located a sizable and diverse literature. A moderate overall ES was calculated. The overall ES is between the values previously reported for older adults and for predominantly healthy adults [11,29]. In subgroup analyses, Dishman and Buckworth reported considerably smaller ESs for the few studies they included of people with cardiac disease. These differences probably reflect population differences among the primary studies. Few primary studies included in this meta-analysis were included in the previously reported syntheses.

The calculated differences in PA minutes per week (164.4 vs. 116.4) and in steps per day (7053 vs. 6108) are clinically meaningful for adults with many chronic illnesses. Although the treatment subjects generally did not achieve the 10,000 steps/day commonly recommended for healthy adults [222,223], the PA dose necessary to achieve health outcomes has not been definitively documented for adults with chronic illness. It is unclear whether people gain the greatest health benefits from initial increases in PA above sedentary rates or from moving from moderate levels of PA to more active levels. The amount of increase is clear evidence that some interventions are effective in changing PA behavior. The extent of heterogeneity documents that not all interventions are equally effective.

Our exploratory moderator analyses documented some intriguing findings. Since the moderator analyses were designed to be hypothesis generating, these findings should be explored in further primary research. The largest ESs came from patient education interventions that were designed exclusively to change PA behavior, as compared to those focused on multiple health behaviors. These findings about effectiveness of PA-only interventions are consistent with a previous meta-analysis of interventions to increase PA among healthy and chronically ill older adults [11]. It may be easier to change one behavior at a time. Chronically ill adults may feel overwhelmed when asked to make multiple changes simultaneously. This finding is for PA behavior outcomes and may not extend to health outcomes. For example, a study of adults with type 1 diabetes found better metabolic control outcomes when interventions focused on multiple diabetes-related health behaviors [218]. In contrast, a previous meta-analysis of people with type 2 diabetes found better metabolic control outcomes when interventions targeted only PA behavior [30]. Attempts to change multiple behaviors may be appropriate when the health benefits of some combination of behavior changes are more important than changes achieved by changing only one behavior. We need further primary research which examines both behavior change and health outcomes of interventions which target single behaviors as compared to those which encourage changing multiple behaviors [224].

The moderator analyses provide evidence that patient education interventions were similarly effective regardless of gender, age, minority, and socioeconomic status. Differences in the ESs of PA among the major categories of chronic illnesses were interesting. Subjects recruited because they had arthritis were the most likely to increase their PA, despite possible immediate arthritis-related physical discomfort associated with doing so. It is possible that arthritis symptoms improve after establishing a PA program, which reinforced PA behavior. People recruited because they had diabetes and cardiac disease improved their PA, though less dramatically. With increased PA, people with diabetes may experience improved blood glucose levels and people with cardiac disease may increase fitness while delaying progression of cardiac disease. These objective health outcomes are clearly important, but they may be less perceptible and persuasive thus providing less motivation to continue PA. Further primary research which tests behavior changes, symptom outcomes, and health consequences of interventions is needed. These findings should be interpreted with the understanding that most studies in this meta-analysis did not exclude subjects with co-morbidities. Subjects recruited for a specific illness often had other diseases as well (e.g. diabetes and cardiac disease is a common combination). Co-morbidities were too infrequently reported to be included in the analyses.

Supervised exercise was the most common intervention strategy, but our moderator analyses revealed that it worked no better than educational/motivational sessions. These findings are consistent with previous meta-analyses of older adults and predominantly healthy adults [11,29]. Supervised exercise is an expensive intervention because it requires specialized facilities and equipment as well as highly trained personnel. For some chronically ill populations or subpopulations (e.g. severe heart failure), supervised exercise may be useful for safety or other reasons.

In our moderator analyses, self-monitoring of PA behavior was associated with larger ESs. A previous meta-analysis of interventions with older adults also found self-monitoring an effective strategy [11]. Self-monitoring provides subjects with real-time information and may increase their awareness of existing behavior as well as changes in behavior. Self-monitoring is an inexpensive strategy. Most other single intervention strategies were not associated with differences in ESs.

The findings regarding behavioral versus cognitive categories of interventions were interesting in light of previous research. These findings are consistent with two previous meta-analyses of healthy and older adults that reported behavior strategies were effective in changing PA [11,29]. Mass media attention to the importance of PA may have raised subjects' consciousness of its value. People may need more behavior change strategies to successfully change PA behavior. Interventions which were found to be effective included varying combinations of goal setting, contracting, feedback, consequences, self-monitoring, and/or prompts. Intervention content that this meta-analysis found to be unrelated to PA behavior change includes decisional balance activities, problem solving, barriers management, motivational counseling, or an emphasis on self-efficacy and outcome expectancy. Future intervention tests that directly compare combinations of behavioral and cognitive strategies are necessary to provide direction for practice. Further primary research which examines mediators of behavior change would help clarify the links between intervention components and outcomes. When considerably more primary research is available, future meta-analyses may be able to address the specific constellation of intervention components that when grouped together make the largest changes in PA behavior.

We were unable to directly address specific theoretical frameworks for several reasons. First, studies often use selected components or language commonly associated with particular theories but fail to name the theory or cite theorists. Thus decisions about including these studies would rely on considerable coder attribution that may not be justified. Conceptual frameworks that address health behavior change have many overlapping constructs. For example, self-efficacy constructs are found in social cognitive theory, the theory of planned behavior, and the transtheoretical model. Some primary reports describe interventions as based on multiple theories. Interventions often only partially implement theoretical frameworks. For example, some studies claim social cognitive theory origins but do not address the sources of self-efficacy. Setting criteria for when interventions are based on the theoretical model would depend entirely on research team opinions and would be difficult to operationalize (e.g. does an intervention need to address three of the four sources of self-efficacy to be based on social cognitive theory?). Given current reporting practices, it is unclear if future quantitative syntheses will be able to fully address conceptual frameworks.

We conducted the first reported analyses of joint moderators and found that this may be effective for discovering patterns among studies (e.g. exercise prescription and fitness testing; age and weeks of intervention, interactions between random allocation and other moderators). Relationships among moderators may be complex. Unfortunately, too little is understood about PA behavior change to suggest meaningful directions for these analyses at this time. This will be an important strategy, after many more primary studies are available, to detect the grouping of intervention strategies that combine to make the most effective intervention.

The methodological findings provide a context for interpreting future studies. ESs were similar between single- and two-group comparisons, though there are many reasons to prefer findings from two-group studies. Previous meta-analyses have not reported ESs for control groups. We found that, on average, the PA behavior of control subjects did not change. Thus, researcher used methods for collecting PA data and delivering information to controls generally did not change PA behavior. We were somewhat surprised to find that attrition was unrelated to ESs, given the folk wisdom that subjects who are not exercising are the most likely to drop out of PA studies. Since no previous meta-analysis has examined attrition, future quantitative syntheses should address this whenever examining health behavior change outcomes. The finding that unfunded studies reported larger ESs is interesting. Unfunded studies may differ in ways other than funding status. For example, unfunded studies may include particularly powerful or novel interventions that researchers pilot tested prior to requesting funding.

These findings should be interpreted within the limitations of this meta-analysis. Funnel plots suggested potential publication bias. It remains unclear whether investigators do not attempt to publish or are unable to publish findings from studies without statistically significant intervention effects [37]. We expected the findings of considerable heterogeneity. These should stimulate continued research to determine which primary study features (e.g. sample, intervention, or design attributes) account for differences among studies. Findings of moderator analyses must be interpreted cautiously in the presence of significant heterogeneity. We do not know the extent to which primary study samples represent populations of chronically ill adults. It is possible that, with safety in mind, investigators recruited participants who were less ill and perhaps more physically active [225]. It is also possible that less active subjects were purposefully recruited [225]. Many important features of studies, such as treatment fidelity, were unreported and thus we could not analyze them. Important potential subject characteristic moderators could not be analyzed because they were infrequently reported. For example, co-morbid medical conditions and mental health issues (e.g. depression) are infrequently reported in primary research but could be important moderators of intervention effects. Systematic testing of findings from moderator analyses from future studies will be important.

4.2 Conclusion

Overall, our quantitative synthesis documented moderate PA behavior effects following diverse patient educational interventions. PA is especially important for adults with chronic illnesses because it may delay progression of some chronic illnesses and manage symptoms of others. Our exploratory moderator analyses have suggested directions for future research. In order to increase knowledge about effective patient education interventions, it is essential to continue conducting new primary research studies as well as quantitative syntheses.

4.3 Practice Implications

Our findings document that patient education intervention can increase PA but that not all interventions are effective. Careful outcome assessments of programs are essential. Patient education programs may be effective across gender, age, and income varied subjects, though adults with diabetes or cardiac disease may be less likely to change their behavior than those with arthritis. The suggestive moderator analyses found associations between PA behavior change and interventions that target only PA behavior, include self-monitoring, and emphasize behavioral strategies such as goal setting, contracting, feedback, consequences, and/or cues. The analyses found that interventions that do not include supervised exercise were as effective as interventions with this more costly component. The importance of increasing PA among many chronically ill adults justifies continuing to develop diverse patient education efforts.

Acknowledgments

Financial support provided by a grant from the National Institutes of Health (R01NR07870) to Vicki Conn, principal investigator.

Footnotes

Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

Contributor Information

Vicki S. Conn, University of Missouri, Columbia, MO, USA 65211.

Adam R. Hafdahl, Washington University

Sharon A. Brown, University of Texas

Lori M. Brown, University of Missouri

References

  • 1.Kroeze W, Werkman A, Brug J. A systematic review of randomized trials on the effectiveness of computer-tailored education on physical activity and dietary behaviors. Ann Behav Med. 2006;31:205–23. doi: 10.1207/s15324796abm3103_2. [DOI] [PubMed] [Google Scholar]
  • 2.Eakin EG, Glasgow RE, Riley KM. Review of primary care-based physical activity intervention studies: effectiveness and implications for practice and future research. J Fam Practice. 2000;49:158–68. [PubMed] [Google Scholar]
  • 3.Eden KB, Orleans CT, Mulrow CD, Pender NJ, Teutsch SM. Does counseling by clinicians improve physical activity? A summary of the evidence for the U.S. Preventive Services Task Force. Ann Intern Med. 2002;137:208E–215E. doi: 10.7326/0003-4819-137-3-200208060-00015. [DOI] [PubMed] [Google Scholar]
  • 4.Lawlor DA, Hanratty B. The effect of physical activity advice given in routine primary care consultations: A systematic review. J Public Health Med. 2001;23:219–26. doi: 10.1093/pubmed/23.3.219. [DOI] [PubMed] [Google Scholar]
  • 5.Morey MC, Sullivan RJ. Medical assessment for health advocacy and practical strategies for exercise initiation. Am J Prev Med. 2003;25(3) 2:204–8. doi: 10.1016/s0749-3797(03)00180-6. [DOI] [PubMed] [Google Scholar]
  • 6.Humpel N, Owen N, Leslie E. Environmental factors associated with adults' participation in physical activity: A review. Am J Prev Med. 2002;22:188–99. doi: 10.1016/s0749-3797(01)00426-3. [DOI] [PubMed] [Google Scholar]
  • 7.Li F, Bauman A, Ory MG, Chodzko-Zajko W. Neighborhood influences on physical activity in middle-aged and older adults: A multilevel perspective. J Aging Phys Activ. 2005;13:87–114. doi: 10.1123/japa.13.1.87. [DOI] [PubMed] [Google Scholar]
  • 8.Marcus BH, Owen N, Forsyth LH, Cavill NA, Firdinger F. Physical activity interventions using mass media, print media, and information technology. Am J Prev Med. 1998;15:362–78. doi: 10.1016/s0749-3797(98)00079-8. [DOI] [PubMed] [Google Scholar]
  • 9.Dunn AL, Andersen RE, Jakicic JM. Lifestyle physical activity interventions. History, short- and long-term effects, and recommendations. Am J Prev Med. 1998;15:398–412. doi: 10.1016/s0749-3797(98)00084-1. [DOI] [PubMed] [Google Scholar]
  • 10.Matson-Koffman DM, Brownstein JN, Neiner JA, Greaney ML. A site-specific literature review of policy and environmental interventions that promote physical activity and nutrition for cardiovascular health: What works? Am J Health Promot. 2005;19:167–93. doi: 10.4278/0890-1171-19.3.167. [DOI] [PubMed] [Google Scholar]
  • 11.Conn V, Valentine J, Cooper H. Interventions to increase physical activity among aging adults: A meta-analysis. Ann Behav Med. 2002;24:190–200. doi: 10.1207/S15324796ABM2403_04. [DOI] [PubMed] [Google Scholar]
  • 12.Van Der Bij AK, Laurant MG, Wensing M. Effectiveness of physical activity interventions for older adults: A review. Am J Prev Med. 2002;22:120–33. doi: 10.1016/s0749-3797(01)00413-5. [DOI] [PubMed] [Google Scholar]
  • 13.American College of Sports Medicine. Physical activity programs and behavior counseling in older adult populations. Med Sci Sport Exer. 2004;36:1997–2003. doi: 10.1249/01.mss.0000145451.08166.97. [DOI] [PubMed] [Google Scholar]
  • 14.Banks-Wallace J, Conn V. Interventions to promote physical activity among African American women. Public Health Nurs. 2002;19:321–35. doi: 10.1046/j.1525-1446.2002.19502.x. [DOI] [PubMed] [Google Scholar]
  • 15.Burnet DL, Elliott LD, Quinn MT, Plaut AJ, Schwartz MA, Chin MH. Preventing diabetes in the clinical setting. J Gen Intern Med. 2006;21:84–93. doi: 10.1111/j.1525-1497.2005.0277.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Coble JD, Rhodes RE. Physical activity and Native Americans: A review. Am J Prev Med. 2006;31:36–46. doi: 10.1016/j.amepre.2006.03.004. [DOI] [PubMed] [Google Scholar]
  • 17.Cress ME, Buchner DM, Prohaska T, Rimmer J, Brown M, Macera C, Dipietro L, Chodzko-Zajko W. Best practices for physical activity programs and behavior counseling in older adult populations. J Aging Phys Activ. 2005;13:61–74. doi: 10.1123/japa.13.1.61. [DOI] [PubMed] [Google Scholar]
  • 18.Cunningham GO, Michael YL. Concepts guiding the study of the impact of the built environment on physical activity for older adults: A review of the literature. Am J Health Promot. 2004;18:435–43. doi: 10.4278/0890-1171-18.6.435. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Marcus BH, Williams DM, Dubbert PM, Sallis JF, King AC, Yancey AK, Franklin BA, Buchner D, Daniels SR, Clayton RP. Physical Activity Intervention Studies, what we know and what we need to know. A scientific statement from the American Heart Association Council on Nutrition, Physical Activity, and Metabolism (Subcommittee on Physical Activity); Council on Cardiovascular Disease in the Young; and the Interdisciplinary Working Group on Quality of Care and Outcomes Research. Circulation. 2006;114:2739–52. doi: 10.1161/CIRCULATIONAHA.106.179683. [DOI] [PubMed] [Google Scholar]
  • 20.Adams J, White M. Are activity promotion interventions based on the transtheoretical model effective? A critical review. Brit J Sport Med. 2003;37:106–114. doi: 10.1136/bjsm.37.2.106. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Epstein LH, Roemmich JN. Reducing sedentary behavior: Role in modifying physical activity. Exerc Sport Sci Rev. 2001;29:103–8. doi: 10.1097/00003677-200107000-00003. [DOI] [PubMed] [Google Scholar]
  • 22.Laitakari J, Miilunpalo S. How can physical activity be changed--basic concepts and general principles in the promotion of health-related physical activity. Patient Educ Couns. 1998;33(1 Suppl):47S–49S. doi: 10.1016/s0738-3991(98)00009-3. [DOI] [PubMed] [Google Scholar]
  • 23.Nupponen R. What is counseling all about--basics in the counseling of health-related physical activity. Patient Educ Couns. 1998;33(1 Suppl):61S–67S. doi: 10.1016/s0738-3991(98)00010-x. [DOI] [PubMed] [Google Scholar]
  • 24.Rinne M, Toropainen E. How to lead a group--practical principles and experiences of conducting a promotional group in health-related physical activity. Patient Educ Couns. 1998;33(1 Suppl):69S–76S. doi: 10.1016/s0738-3991(98)00011-1. [DOI] [PubMed] [Google Scholar]
  • 25.Dunn AL. Getting started--a review of physical activity adoption studies. Brit J Sport Med. 1996;30:193–9. doi: 10.1136/bjsm.30.3.193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Kahn EB, Ramsey LT, Brownson RC, Heath GW. The effectiveness of interventions to increase physical activity. A systematic review. Am J Prev Med. 2002;22(4 Suppl):73–107. doi: 10.1016/s0749-3797(02)00434-8. [DOI] [PubMed] [Google Scholar]
  • 27.Hillsdon M, Foster C, Thorogood M. Interventions for promoting physical activity. Cochrane Db Syst Rev. 2005;(1):CD003180. doi: 10.1002/14651858.CD003180.pub2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Ashworth NL, Chad KE, Harrison EL, Reeder BA, Marshall SC. Home versus center based physical activity programs in older adults. Cochrane Db Syst Rev. 2005;(1):CD00401. doi: 10.1002/14651858.CD004017.pub2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Dishman RK, Buckworth J. Increasing physical activity: A quantitative synthesis. Med Sci Sport Exer. 1996;28:706–19. doi: 10.1097/00005768-199606000-00010. [DOI] [PubMed] [Google Scholar]
  • 30.Conn V, Hafdahl A, Mehr D, LeMaster J, Brown S, Nielsen P. Meta-analysis of metabolic effects of interventions to increase exercise among adults with type 2 diabetes. Diabetologia. 2007;50:913–21. doi: 10.1007/s00125-007-0625-0. [DOI] [PubMed] [Google Scholar]
  • 31.Conn V, Hafdahl A, Porock D, McDaniel R, Nielsen P. A meta-analysis of exercise interventions among people treated for cancer. Support Care Cancer. 2006;14:699–712. doi: 10.1007/s00520-005-0905-5. [DOI] [PubMed] [Google Scholar]
  • 32.Cooper H, Hedges L, editors. The handbook of research synthesis. New York: Russell Sage Foundation; 1994. [Google Scholar]
  • 33.Hedges L, Olkin I. Statistical methods for meta-analysis. Orlando: Academic Press; 1985. [Google Scholar]
  • 34.Morris SB. Distribution of the standardized mean change effect size for meta-analysis on repeated measures. Brit J Math Stat Psy. 2000;53:17–29. doi: 10.1348/000711000159150. [DOI] [PubMed] [Google Scholar]
  • 35.Nielsen P, Hafdahl A, Conn V, LeMaster J, Brown S. Meta-analysis of the effect of exercise interventions on fitness outcomes among adults with type 1 and type 2 diabetes. Diabetes Res Clin Pr. 2006;74:111–20. doi: 10.1016/j.diabres.2006.03.033. [DOI] [PubMed] [Google Scholar]
  • 36.Conn V, Isamaralai S, Rath S, Jantarakupt P, Wadhawan R, Dash Y. Beyond MEDLINE for literature searches. J Nurs Scholarsh. 2003;35:177–82. doi: 10.1111/j.1547-5069.2003.00177.x. [DOI] [PubMed] [Google Scholar]
  • 37.Conn V, Valentine J, Cooper H, Rantz M. Grey literature in meta-analyses. Nurs Res. 2003;52:256–61. doi: 10.1097/00006199-200307000-00008. [DOI] [PubMed] [Google Scholar]
  • 38.Brown SA, Upchurch S, Anding R, Winter M. Promoting weight loss in type II diabetes. Diabetes Care. 1996;19:613–24. doi: 10.2337/diacare.19.6.613. [DOI] [PubMed] [Google Scholar]
  • 39.Dusseldorp E, Van Elderen T, Maes S, Meulman J, Kraaij V. A meta-analysis of psychoeducational programs for coronary heart disease patients. Health Psychol. 1999;18:506–19. doi: 10.1037//0278-6133.18.5.506. [DOI] [PubMed] [Google Scholar]
  • 40.Little JH, Popa M, Forsythe B. Multisystemic therapy for social, emotional, and behavioral problems in youth aged 10-17. Cochrane Db Syst Rev. 2005;(3):CD004797. doi: 10.1002/14651858.CD004797.pub3. [DOI] [PubMed] [Google Scholar]
  • 41.Merry S, McDowell H, Hetrick S, Bir J, Muller N. Psychological and/or educational interventions for the prevention of depression in children and adolescents. Cochrane Db Syst Rev. 2004;(1):CD003380. doi: 10.1002/14651858.CD003380.pub2. [DOI] [PubMed] [Google Scholar]
  • 42.Norris SL, Zhang X, Avenell A, Gregg E, Schmid CH, Lau J. Long-term non-pharmacological weight loss interventions for adults with prediabetes. Cochrane Db Syst Rev. 2005;(2):CD005270. doi: 10.1002/14651858.CD005270. [DOI] [PubMed] [Google Scholar]
  • 43.Royal ST, Kendrick D, Coleman T. Non-legislative interventions for the promotion of cycle helmet wearing by children. Cochrane Db Syst Rev. 2005;(2):CD003985. doi: 10.1002/14651858.CD003985.pub2. [DOI] [PubMed] [Google Scholar]
  • 44.Colditz GA, Burdick E, Mosteller F. Heterogeneity in meta-analysis of data from epidemiologic studies: A commentary. Am J Epidemiol. 1995;142:371–82. doi: 10.1093/oxfordjournals.aje.a117644. [DOI] [PubMed] [Google Scholar]
  • 45.Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analysis. Brit Med J. 2003;327:557–60. doi: 10.1136/bmj.327.7414.557. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Berlin JA. Invited commentary: Benefits of heterogeneity in meta-analysis of data from epidemiologic studies. Am J Epidemiol. 1995;142:383–7. doi: 10.1093/oxfordjournals.aje.a117645. [DOI] [PubMed] [Google Scholar]
  • 47.Lipsey M, Wilson D. Practical meta-analysis. Thousand Oaks: Sage; 2001. [Google Scholar]
  • 48.Lipsey M, Wilson D. The way in which intervention studies have “personality” and why it is important to meta-analysis. Eval Health Prof. 2001;24:236–54. doi: 10.1177/016327870102400302. [DOI] [PubMed] [Google Scholar]
  • 49.Morris SB, DeShon RP. Combining effect size estimates in meta-analysis with repeated measures and independent-groups designs. Psychol Methods. 2002;2:105–125. doi: 10.1037/1082-989x.7.1.105. [DOI] [PubMed] [Google Scholar]
  • 50.Gleser LJ, Olkin I. Stochastically dependent effect sizes. In: Cooper H, Hedges L, editors. The handbook of research synthesis. New York: Russell Sage Foundation; 1994. pp. 339–355. [Google Scholar]
  • 51.Vevea JL, Hedges LV. A general linear model for estimating effect size in the presence of publication bias. Psychometrika. 1995;60:419–435. [Google Scholar]
  • 52.Kline RB. Beyond significance testing: reforming data analysis methods in behavioral research. Washington, DC: American Psychological Association; 2004. [Google Scholar]
  • 53.Hedges L. Fixed effects models. In: Cooper H, Hedges L, editors. The handbook of research synthesis. New York: Russell Sage Foundation; 1994. pp. 285–299. [Google Scholar]
  • 54.Raudenbush SW. Random effects models. In: Cooper H, Hedges L, editors. The handbook of research synthesis. New York: Russell Sage Foundation; 1994. pp. 301–321. [Google Scholar]
  • 55.Agurs-Collins TD, Kumanyika SK, Ten Have TR, Adams-Campbell LL. A randomized controlled trial of weight reduction and exercise for diabetes management in older African-American subjects. Diabetes Care. 1997;20:1503–1511. doi: 10.2337/diacare.20.10.1503. [DOI] [PubMed] [Google Scholar]
  • 56.Allen J. Coronary risk factor modification in women after coronary artery bypass surgery. Nurs Res. 1996;45:260–265. doi: 10.1097/00006199-199609000-00002. [DOI] [PubMed] [Google Scholar]
  • 57.Allison MJ. The effect of a social cognitive theory-based intervention on self-efficacy and physical activity in older adults post coronary event [Dissertation] San Antonio, TX: University of Texas; 2000. [Google Scholar]
  • 58.Allison T, Farkouh M, Smars P, Evans R, Squires R, Gabriel S, Kopecky S, Gibbons R, Reeder G. Management of coronary risk factors by registered nurses versus usual care in patients with unstable angina pectoris. Am J Cardiol. 2000;86:133–138. doi: 10.1016/s0002-9149(00)00848-1. [DOI] [PubMed] [Google Scholar]
  • 59.Allison TG, Squires RW, Johnson BD, Gau GT. Achieving National Cholesterol Education Program goals for low-density lipoprotein cholesterol in cardiac patients: importance of diet, exercise, weight control, and drug therapy. Mayo Clin Proc. 1999;74:466–473. doi: 10.4065/74.5.466. [DOI] [PubMed] [Google Scholar]
  • 60.Appel LJ, Champagne CM, Harsha DW, Cooper LS, Oberzanek E, Elmer PJ, Stevens VJ, Vollmer WM, Lin PH, Svetkey LP, Stedman SW, Young DR. Effects of comprehensive lifestyle modification on blood pressure control: main results of the PREMIER clinical trial. JAMA. 2003;289:2083–2093. doi: 10.1001/jama.289.16.2083. [DOI] [PubMed] [Google Scholar]
  • 61.Arroll B, Beaglehole R. Salt restriction and physical activity in treated hypertensives. N Z Med J. 1995;108:266–268. [PubMed] [Google Scholar]
  • 62.Baker KR, Nelson ME, Felson DT, Layne JE, Sarno R, Roubenoff R. The efficacy of home based progressive strength training in older adults with knee osteoarthritis: a randomized controlled trial. J Rheumatol. 2001;28:1655–1665. [PubMed] [Google Scholar]
  • 63.Barlow JH, Turner AP, Wright CC. A randomized controlled study of the Arthritis Self-Management Programme in the UK. Health Educ Res. 2000;15:665–680. doi: 10.1093/her/15.6.665. [DOI] [PubMed] [Google Scholar]
  • 64.Barnason S, Zimmerman L, Nieveen J, Schmaderer M, Carranza B, Reilly S. Impact of a home communication intervention for coronary artery bypass graft patients with ischemic heart failure on self-efficacy, coronary disease risk factor modification, and functioning. Heart Lung. 2003;32:147–158. doi: 10.1016/s0147-9563(03)00036-0. [DOI] [PubMed] [Google Scholar]
  • 65.Beebe C, Fischer B, McCracken S. Lifestyle change: a new approach to treatment of obese type II diabetes? Diabetes. 1984;24 6A [Google Scholar]
  • 66.Bengtsson K. Rehabilitation after myocardial infarction. A controlled study. Scand J Rehabil Med. 1983;15:1–9. [PubMed] [Google Scholar]
  • 67.Bennett R, Burckhardt C, Clark S, O'Reilly C, Wiens A, Campbell S. Group treatment for fibromyalgia: a 6 month outpatient program. J Rheumatol. 1996;23:521–528. [PubMed] [Google Scholar]
  • 68.Bielamowicz M, Miller W, Elkins E, Ladeqig H. Monitoring behavioral changes in diabetes care with the diabetes self-management record. Diabetes Educ. 1995;21:426–431. doi: 10.1177/014572179502100506. [DOI] [PubMed] [Google Scholar]
  • 69.Bock BC, Carmona-Barros RE, Esler JL, Tilkemeier PL. Program participation and physical activity maintenance after cardiac rehabilitation. Behav Modif. 2003;27:37–53. doi: 10.1177/0145445502238692. [DOI] [PubMed] [Google Scholar]
  • 70.Bock B, Albrecht A, Traficante R, Clark M, Pinto B, Tilkemeier P, Marcus B. Predictors of exercise adherence following participation in a cardiac rehabilitation program. Int J Behav Med. 1997;4:60–75. doi: 10.1207/s15327558ijbm0401_4. [DOI] [PubMed] [Google Scholar]
  • 71.Brus HL, van de Laar M, Taal E, Rasker J, Wiegman O. Effects of patient education on compliance with basic treatment regimens and health in recent onset active rheumatoid arthritis. Ann Rheum Dis. 1998;57:146–151. doi: 10.1136/ard.57.3.146. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Burge MR, Hewes H, Araiza P, Gashytewa C. Efficacy of a pedometer based physical activity program on parameters of diabetes control in type 2 diabetes; American Diabetes Association Scientific Session; Boston. 2002. [DOI] [PubMed] [Google Scholar]
  • 73.Campbell NC, Ritchie LD, Thain J, Deans HG, Rawles JM, Squair JL. Secondary prevention in coronary heart disease: a randomised trial of nurse led clinics in primary care. Heart. 1998;80:447–452. doi: 10.1136/hrt.80.5.447. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Cantagallo A, Cignetti A, Garbuio B, Giancotta V. How long does the efficacy of therapeutic education last? Four-year-follow up; Paper presented at the 18th International Diabetes Federation Congress; 2003. [Google Scholar]
  • 75.Carlsson R, Lindberg G, Westin L, Israelsson B. Influence of coronary nursing management follow up on lifestyle after acute myocardial infarction. Heart. 1997;77:256–259. doi: 10.1136/hrt.77.3.256. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Castaneda C, Layne JE, Munoz-Orians L, Gordon PL, Walsmith J, Foldvari M, Roubenoff R, Tucker K, Nelson M. A randomized controlled trial of progressive resistance exercise training to improve glycemic control in older adults with type 2 diabetes. Diabetes Care. 2002;25:2335–2341. doi: 10.2337/diacare.25.12.2335. [DOI] [PubMed] [Google Scholar]
  • 77.Clark M, Hampson SE, Avery L, Simpson R. Effects of a tailored lifestyle self-management intervention in patients with Type 2 diabetes. Br J Health Psychol. 2004;9:365–379. doi: 10.1348/1359107041557066. [DOI] [PubMed] [Google Scholar]
  • 78.Conn V, Burks K, Minor M, Mehr D. Randomized trial of two interventions to increase older women's exercise. Am J Health Behav. 2003;27:380–388. doi: 10.5993/ajhb.27.4.10. [DOI] [PubMed] [Google Scholar]
  • 79.Courneya KS, Friedenreich CM, Quinney HA, Fields AL, Jones LW, Fairey AS. A randomized trial of exercise and quality of life in colorectal cancer survivors. Eur J Cancer Care. 2003;12:347–357. doi: 10.1046/j.1365-2354.2003.00437.x. [DOI] [PubMed] [Google Scholar]
  • 80.Cox N, Hendricks J, Binkhorst R, van Herwaarden C. A pulmonary rehabilitation program for patients with asthma and mild chronic obstructive pulmonary disease. Lung. 1993;171:235–244. doi: 10.1007/BF00203723. [DOI] [PubMed] [Google Scholar]
  • 81.Cupples ME, McKnight A. Randomised controlled trial of health promotion in general practice for patients at high cardiovascular risk. Br Med J. 1994;309:993–996. doi: 10.1136/bmj.309.6960.993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82.DeVellis BM, Blalock SJ, Hahn PM, DeVellis RF, Hochbaum G. Evaluation of a problem-solving intervention for patients with arthritis. Patient Educ Couns. 1988;11:29–42. [Google Scholar]
  • 83.Dilsen G, Berker C, Oral A, Varan G. The role of physical exercise in prevention and management of osteoporosis. Clin Rheumatol. 1989;8:70–75. doi: 10.1007/BF02207238. [DOI] [PubMed] [Google Scholar]
  • 84.Djuric Z, DiLaura NM, Bradley E, Hryniuk W. Weight loss intervention in African American breast cancer survivors. Presented at Amer Soc Prev Oncolog; 2003. [Google Scholar]
  • 85.Dolansky MA. Effects of cardiac rehabilitation on older adults' recovery outcomes following coronary artery bypass surgery [Dissertation] Cleveland, OH: Case Western Reserve University; 2001. [Google Scholar]
  • 86.Dubbert P, Cooper K, Kirchner K, Meydrech E, Bilbrew D. Effects of nurse counseling on walking for exercise in elderly primary care patients. J Gerontol. 2002;57A:M733–M740. doi: 10.1093/gerona/57.11.m733. [DOI] [PubMed] [Google Scholar]
  • 87.Duncan K, Pozehl B. Effects of an exercise adherence intervention on outcomes in patients with heart failure. Rehabil Nurs. 2003;28:117–122. doi: 10.1002/j.2048-7940.2003.tb01728.x. [DOI] [PubMed] [Google Scholar]
  • 88.Dunstan DW, Daly RM, Owen N, Jolley D, De Courten M, Shaw J, Zimmet P. High-intensity resistance training improves glycemic control in older patients with type 2 diabetes. Diabetes Care. 2002;25:1729–1736. doi: 10.2337/diacare.25.10.1729. [DOI] [PubMed] [Google Scholar]
  • 89.Engelhart M, Kondrup J, Hoie LH, Andersen V, Kristensen JH, Heitmann BL. Weight reduction in obese patients with rheumatoid arthritis, with preservation of body cell mass and improvement of physical fitness. Clin Exp Rheumatol. 1996;14:289–293. [PubMed] [Google Scholar]
  • 90.Erdman R, Duivenvoordent H, Verhage F. Predictability of beneficial effects in cardiac rehabilitation: a randomized clinical trial of psychosocial variables. J Cardiopulm Rehabil. 1986;6:206–213. [Google Scholar]
  • 91.Ersek M, Turner J, McCurry S, Gibbons L, Kraybill B. Efficacy of a self-management group intervention for elderly persons with chronic pain. Clin J Pain. 2003;19:156–167. doi: 10.1097/00002508-200305000-00003. [DOI] [PubMed] [Google Scholar]
  • 92.French SL. The self-management of osteoarthritis in older women: a study of the efficacy of the Arthritis Self-Management Program and of the factors influencing outcomes. Queen's University; Kingston, Ontario: 1996. [Google Scholar]
  • 93.Fries JF, Carey C, McShane DJ. Patient education in arthritis: randomized controlled trial of a mail-delivered program. J Rheumatol. 1997;24:1378–1383. [PubMed] [Google Scholar]
  • 94.Gaede P, Beck M, Vedel P, Petersen O. Limited impact of lifestyle education in patients with Type 2 diabetes mellitus and microalbuminuria: results from a randomized intervention study. Diabet Med. 2001;18:104–108. doi: 10.1046/j.1464-5491.2001.00444.x. [DOI] [PubMed] [Google Scholar]
  • 95.Gardner AW, Katzel LI, Sorkin JD, Killewich L, Ryan A, Flinn W, Goldberg A. Improved functional outcomes following exercise rehabilitation in patients with intermittent claudication. J Gerontol. 2000;55A:M570–M577. doi: 10.1093/gerona/55.10.m570. [DOI] [PubMed] [Google Scholar]
  • 96.Gardner AW, Katzel LI, Sorkin JD, Golderg AP. Effects of long-term exercise rehabilitation on claudication distances in patients with peripheral arterial disease: a randomized controlled trial. J Cardiopulm Rehabil. 2002;22:192–198. doi: 10.1097/00008483-200205000-00011. [DOI] [PubMed] [Google Scholar]
  • 97.Gardner AW, Killewich LA, Montgomery PS, Katzel LI. Response to exercise rehabilitation in smoking and nonsmoking patients with intermittent claudication. J Vasc Surg. 2004;39:531–538. doi: 10.1016/j.jvs.2003.08.037. [DOI] [PubMed] [Google Scholar]
  • 98.Gardner AW, Pillai SB, Sieminski DJ, Muir J, Cowell LL, Montgomery PS. Daily physical activity of peripheral arterial disease patients is increased following exercise rehabilitation; Paper presented at the American College of Sports Medicine: Minneapolis; Minnesota. 2001. [Google Scholar]
  • 99.Gary TL, Bone LR, Hill M, Levine D, McGuire M, Saudek C, Brancati F. A randomized controlled trial of the effects of nurse case manager and community health worker team interventions in urban African-Americans with type 2 diabetes. Prev Med. 2003;37:23–32. doi: 10.1016/s0091-7435(03)00040-9. [DOI] [PubMed] [Google Scholar]
  • 100.Giese H, Helgo Schomer H. Life-style changes and mood profile of cardiac patients after an exercise rehabilitation program. J Cardiopulm Rehabil. 1986;6:30–37. [Google Scholar]
  • 101.Glasgow RE, Toobert DJ, Hampson SE, Brown JE, Lewinsohn PM, Donnelly J. Improving self-care among older patients with Type II diabetes: the “Sixty Something” study. Patient Educ Couns. 1992;19:61–74. doi: 10.1016/0738-3991(92)90102-o. [DOI] [PubMed] [Google Scholar]
  • 102.Goodwin P, Esplen MJ, Butler K, Winocur J, Pritchard K, Brazel S, Gao J, Miller A. Multidisciplinary weight management in locoregional breast cancer: results of a phase II study. Breast Cancer Res Treat. 1998;48:53–64. doi: 10.1023/a:1005942017626. [DOI] [PubMed] [Google Scholar]
  • 103.Guare JC. Response of obese nondiabetic and diabetic women to behavioral weight loss therapy (Diabetes Mellitus, Weight Loss) [Dissertation] Pittsburgh, PA: University of Pittsburgh; [Google Scholar]
  • 104.Gulanick M. Is phase 2 cardiac rehabilitation necessary for early recovery of patients with cardiac disease? A randomized, controlled study. Heart Lung. 1991;20:9–15. [PubMed] [Google Scholar]
  • 105.Haber D, Lacy M. Evaluation of a socio-behavioral intervention for changing health behaviors of older adults. Behavior, Health, and Aging. 1993;3:73–85. [Google Scholar]
  • 106.Hakkinen A, Sokka T, Hannonen P. A home-based two-year strength training period in early rheumatoid arthritis led to good long-term compliance: a five-year followup. Arthritis Rheum. 2004;51:56–62. doi: 10.1002/art.20088. [DOI] [PubMed] [Google Scholar]
  • 107.Haldorsen E, Kronholm K, Skouen J, Ursin H. Multimodal cognitive behavioral treatment for patients sicklisted for musculoskeletal pain. Scand J Rheumatol. 1998;27:16–25. doi: 10.1080/030097498441128. [DOI] [PubMed] [Google Scholar]
  • 108.Hall JL. Psychological interventions for exercise and dietary behavior change with breast cancer survivors. Philadelphia, PA: Temple University; 1999. [Google Scholar]
  • 109.Hambrecht R, Niebauer J, Fiehn E, Kalberer B, Offner B, Hauer K, Riede U, Schlierf G, Kubler W, Schuler G. Physical training in patients with stable chronic heart failure: effects on cardiorespiratory fitness and ultrastructural abnormalities of leg muscles. J Am Coll Cardiol. 1995;25:1239–1249. doi: 10.1016/0735-1097(94)00568-B. [DOI] [PubMed] [Google Scholar]
  • 110.Hambrecht R, Niebauer J, Marburger C, Grunze M, Kalberer B, Hauer K, Schlierf G, Kubler W, Schuler G. Various intensities of leisure time physical activity in patients with coronary artery disease: effects on cardiorespiratory fitness and progression of coronary atherosclerotic lesions. J Am Coll Cardiol. 1993;22:468–477. doi: 10.1016/0735-1097(93)90051-2. [DOI] [PubMed] [Google Scholar]
  • 111.Handberg-Thurmond EM. Effect of home exercise intervention on functional capacity and quality of life in decompensated heart failure [Dissertation] Gainesville, FL: University of Florida; 1998. [Google Scholar]
  • 112.Hanefeld M, Fischer S, Schmechel H, Rothe G, Schultze J, Dude H, Schwanebeck U, Julius U. Diabetes intervention study: multi-intervention trial in newly diagnosed NIDDM. Diabetes Care. 1991;14:308–317. doi: 10.2337/diacare.14.4.308. [DOI] [PubMed] [Google Scholar]
  • 113.Haskell W, Alderman E, Fair J. Effects of intensive multiple risk factor reduction on coronary artherosclerosis and clinical cardiac events in men and women with coronary artery disease. The Stanford Coronary Risk Intervention Project (SCRIP) Circulation. 1994;89:975–990. doi: 10.1161/01.cir.89.3.975. [DOI] [PubMed] [Google Scholar]
  • 114.Hasler T, Fisher B, MacIntyre N. Exercise consultation and physical activity in patients with type 1 diabetes. Pract Diab Int. 2000;17:44–48. [Google Scholar]
  • 115.Heath G, Maloney P, Fure C. Group exercise versus home exercise in coronary artery bypass graft patients: effects on physical activity habits. J Cardiopulm Rehabil. 1987;7:190–195. [Google Scholar]
  • 116.Helboastad J, Sletvoid O, Moe-Nilssen R. Home training with and without additional group training in physically frail old people living at home: effect on health-related quality of life and ambulation. Clin Rehabil. 2004;18:498–5008. doi: 10.1191/0269215504cr761oa. [DOI] [PubMed] [Google Scholar]
  • 117.Heller RF, Knapp JC, Valenti LA, Dobson AJ. Secondary prevention after acute myocardial infarction. Am J Cardiol. 1993;72:759–762. doi: 10.1016/0002-9149(93)91058-p. [DOI] [PubMed] [Google Scholar]
  • 118.Himeno E, Nishimo K, Okazaki T, Nanri H, Ikeda M. A weight reduction and weight maintenance program with long-lasting improvement in left ventricular mass and blood pressure. Am J Hypertens. 1999;12:682–690. doi: 10.1016/s0895-7061(99)00047-3. [DOI] [PubMed] [Google Scholar]
  • 119.Hogue C, Cullinan S. Exercise training for frail rural elderly. In: Funk SG, Tornquist ET, Champagne MT, Wiese R, editors. Key aspects of caring for the chronically ill: hospital and home. New York: Springer; 1993. pp. 202–211. [Google Scholar]
  • 120.Hopper DL. The effects of telephone contact on the exercise adherence of cardiac patients [Dissertation] Denver, CO: University of Denver; 1995. [Google Scholar]
  • 121.Hughes SL, Seymour RB, Campbell R, Pollak N, Huber G, Sharma L. Impact of the fit and strong intervention on older adults with osteoarthritis. Gerontologist. 2004;44:217–228. doi: 10.1093/geront/44.2.217. [DOI] [PubMed] [Google Scholar]
  • 122.Irvine A, Mitchell C. Impact of community-based diabetes education on program attenders and nonattenders. Diabetes Educ. 1992;18:29–33. doi: 10.1177/014572179201800105. [DOI] [PubMed] [Google Scholar]
  • 123.Iwamoto J, Takeda T, Ichimura S. Effect of exercise training and detraining on bone mineral density in postmenopausal women with osteoporosis. J Orthop Sci. 2001;6:128–132. doi: 10.1007/s007760100059. [DOI] [PubMed] [Google Scholar]
  • 124.Jerant AF, Azari R, Martinez C, Nesbitt TS. A randomized trial of telenursing to reduce hospitalization for heart failure: patient-centered outcomes and nursing indicators. Home Health Care Serv Q. 2003;22:1–20. doi: 10.1300/J027v22n01_01. [DOI] [PubMed] [Google Scholar]
  • 125.Johnson R. The effect of contingency contracting on compliance to the medical regimen in hypertensive black females [Thesis] Denton, TX: Texas Woman's University; 1993. [Google Scholar]
  • 126.Kamwendo K, Tingstrom P, Bergdahl B, Svensson E. Effect of problem-based learning on stages of change for exercise behaviour in patients with coronary artery disease. Physiother Res Int. 2004;9:24–32. doi: 10.1002/pri.297. [DOI] [PubMed] [Google Scholar]
  • 127.Karlovich I, Kholodova H, Mokhort T. Rehabilitation of Type 1 diabetic patients: the experience of rehabilitation diabetologic centre in Belarus; Paper presented at the 18th International Diabetes Federation Congress; Paris-France. 2003. [Google Scholar]
  • 128.Kentala E. Physical fitness and feasibility of physical rehabilitation after myocardial infarction in men of working age. Ann Clin Res. 1972;4 9:1–84. [PubMed] [Google Scholar]
  • 129.Ketelaars C, Abu-Saad H, Halfens R, Schlosser M, Mostert R, Wounters E. Effects of specialized community nursing care in patients with chronic obstructive pulmonary disease. Heart Lung. 1998;27:109–120. doi: 10.1016/s0147-9563(98)90018-8. [DOI] [PubMed] [Google Scholar]
  • 130.Keyserling TC, Samuel-Hodge CD, Ammerman AS, Ainsworth BE, Henriquez-Roldan CF, Elasy TA, Skelly AH, Johnston LF, Bangdiwala SI. A randomized trial of an intervention to improve self-care behaviors of African-American women with type 2 diabetes: impact on physical activity. Diabetes Care. 2002;25:1576–1583. doi: 10.2337/diacare.25.9.1576. [DOI] [PubMed] [Google Scholar]
  • 131.Kochevar A, Smith K, Bernard M. Effects of a community-based intervention to increase activity in American Indian elders. J Okla State Med Assoc. 2001;94:455–460. [PubMed] [Google Scholar]
  • 132.Koertge J, Weidner G, Elliott-Eller M, Scherwitz L, Merritt-Worden TA, Marlin R, Lipsenthal L, Guarneri M, Finkel R, Saunders DE, Jr, McCormac P, Scheer JM, Collins RE, Ornish D. Improvement in medical risk factors and quality of life in women and men with coronary artery disease in the Multicenter Lifestyle Demonstration Project. Am J Cardiol. 2003;91:1316–1322. doi: 10.1016/s0002-9149(03)00320-5. [DOI] [PubMed] [Google Scholar]
  • 133.Laaksonen DE, Atalay M, Niskanen L, Mustonen J, Sen S, Lakka T, Uusitupa M. Aerobic exercise and the lipid profile in type 1 diabetic men: a randomized controlled trial. Med Sci Sport Exerc. 2000;32:1541–1548. doi: 10.1097/00005768-200009000-00003. [DOI] [PubMed] [Google Scholar]
  • 134.Lear SA, Ignaszewski A, Laquer EA, Pritchard PH, Frohlich JJ. Extensive lifestyle management intervention following cardiac rehabilitation: pilot study. Rehabil Nurs. 2001;26:227–232. doi: 10.1002/j.2048-7940.2001.tb01960.x. [DOI] [PubMed] [Google Scholar]
  • 135.Lear SA, Ignaszewski A, Linden W, Brozic A, Kiess M, Spinelli JJ, Haydn Pritchard P, Frohlich JJ. The Extensive Lifestyle Management Intervention (ELMI) following cardiac rehabilitation trial. Eur Heart J. 2003;24:1920–1927. doi: 10.1016/j.ehj.2003.08.015. [DOI] [PubMed] [Google Scholar]
  • 136.Lehmann R, Kaplan V, Bingisser R, Block K, Spinas G. Impact of physical activity on cardiovascular risk factors in IDDM. Diabetes Care. 1997;20:1603–1611. doi: 10.2337/diacare.20.10.1603. [DOI] [PubMed] [Google Scholar]
  • 137.Lehmann R, Engler H, Honegger R, Riesen W, Spinas GA. Alterations of lipolytic enzymes and high-density lipoprotein subfractions induced by physical activity in type 2 diabetes mellitus. Eur J of Clin Invest. 2001;31:37–44. doi: 10.1046/j.1365-2362.2001.00752.x. [DOI] [PubMed] [Google Scholar]
  • 138.Lehmann R, Vokac A, Niedermann K, Agosti K, Spinas GA. Loss of abdominal fat and improvement of the cardiovascular risk profile by regular moderate exercise training in patients with NIDDM. Diabetologia. 1995;38:1313–1319. doi: 10.1007/BF00401764. [DOI] [PubMed] [Google Scholar]
  • 139.Lemozy-Cadroy S, Crognier S, Gourdy P, Chauchard M, Chale J, Tauber J, Hanaire-Broutin H. Intensified treatment of type 1 diabetes: prospective evaluation at one year of a therapeutic patient education programme. Diabetes Metab. 2002;28:287–294. [PubMed] [Google Scholar]
  • 140.Leveille S, Wagner E, Davis ZC, Grothaus L, Wallace J, LoGerfo M, Kent D. Preventing disability and managing chronic illness in frail older adults: a randomized trial of a community-based partnership with primary care. J Am Geriatr Soc. 1998;46:1191–1198. doi: 10.1111/j.1532-5415.1998.tb04533.x. [DOI] [PubMed] [Google Scholar]
  • 141.Ligtenberg PC, Hoekstra JB, Bol E, Zonderland ML, Erkelens DW. Effects of physical training on metabolic control in elderly type 2 diabetes mellitus patients. Clin Sci. 1997;93:127–135. doi: 10.1042/cs0930127. [DOI] [PubMed] [Google Scholar]
  • 142.Lindroth Y, Bauman A, Barnes C, McCredie M, Brooks PM. A controlled evaluation of arthritis education. Br J Rheumatol. 1989;28:7–12. doi: 10.1093/rheumatology/28.1.7. [DOI] [PubMed] [Google Scholar]
  • 143.Linton S, Hellsing A, Bergstrom G. Exercise for workers with musculoskeletal pain: does enhancing compliance decrease pain? J Occup Rehabil. 1996;6:177–190. doi: 10.1007/BF02110754. [DOI] [PubMed] [Google Scholar]
  • 144.Lisspers J, Hofman-Bang C, Nordlander R, Ryden L, Sundin O, Ohman A, Nygren A. Multifactorial evaluation of a program for lifestyle behavior change in rehabilitation and secondary prevention of coronary artery disease. Scand Cardiovasc J. 1999;33:9–16. doi: 10.1080/14017439950141975. [DOI] [PubMed] [Google Scholar]
  • 145.Lloys A, Hickie I, Brockman A, Hickie C, Wilson A, Dwyer J, Wakefield D. Immunologic and psychologic therapy for patients with chronic fatigue syndrome: a double-blind, placebo-controlled trial. Am J Med. 1993;94:197–203. doi: 10.1016/0002-9343(93)90183-p. [DOI] [PubMed] [Google Scholar]
  • 146.Loreto C, Fanelli C, Lucidi P, Murdolo G, DeCicco A, Parlanti N, Santeusanio F, Brunetti P, De Feo P. Validation of a counseling strategy to promote the adoption and the maintenance of physical activity by type 2 diabetic subjects. Diabetes Care. 2003;26:404–408. doi: 10.2337/diacare.26.2.404. [DOI] [PubMed] [Google Scholar]
  • 147.Lorig KR, Sobel DS, Stewart AL, Brown BW, Jr, Bandura A, Ritter P, Gonzalez VM, Laurent DD, Holman HR. Evidence suggesting that a chronic disease self-management program can improve health status while reducing hospitalization: a randomized trial. Med Care. 1999;37:5–14. doi: 10.1097/00005650-199901000-00003. [DOI] [PubMed] [Google Scholar]
  • 148.Lorig KR, Feigenbaum P, Regan C, Ung E, Chastain RL, Holman HR. A comparison of lay-taught and professional-taught arthritis self-management courses. J Rheumatol. 1986;13:763–767. [PubMed] [Google Scholar]
  • 149.Lorig K, Gonzalez VM, Ritter P. Community-based Spanish language arthritis education program: a randomized trial. Med Care. 1999;37:957–963. doi: 10.1097/00005650-199909000-00011. [DOI] [PubMed] [Google Scholar]
  • 150.Lorig K, Gonzalez VM, Laurent DD, Morgan L, Laris BA. Arthritis self-management program variations: three studies. Arthritis Care Res. 1998;11:448–454. doi: 10.1002/art.1790110604. [DOI] [PubMed] [Google Scholar]
  • 151.Lorig K, Lubeck D, Kraines R, Seleznick M, Holman H. Outcomes of self-help education for patients with arthritis. Arthritis Rheum. 1985;28:680–685. doi: 10.1002/art.1780280612. [DOI] [PubMed] [Google Scholar]
  • 152.Lorig K, Seleznick M, Lubeck D, Ung E, Chastain RL, Holman HR. The beneficial outcomes of the arthritis self-management course are not adequately explained by behavior change. Arthritis Rheum. 1989;32:91–95. doi: 10.1002/anr.1780320116. [DOI] [PubMed] [Google Scholar]
  • 153.Lorig K, Sobel D, Ritter P, Laurent D, Hobbs M. Effect of a self-management program on patients with chronic disease. Eff Clin Pract. 2001;4:256–262. [PubMed] [Google Scholar]
  • 154.Maeland JG, Havik OE. The effects of an in-hospital educational programme for myocardial infarction patients. Scand J Rehabil Med. 1997;19:57–65. [PubMed] [Google Scholar]
  • 155.Mahler HI, Kulik JA, Tarazi RY. Effects of a videotape information intervention at discharge on diet and exercise compliance after coronary bypass surgery. J Cardiopulm Rehabil. 1999;19:170–177. doi: 10.1097/00008483-199905000-00004. [DOI] [PubMed] [Google Scholar]
  • 156.Marshall AL, Booth ML, Bauman AE. Promoting physical activity in Australian general practices: a randomised trial of health promotion advice versus hypertension management. Patient Educ Couns. 2005;56:283–290. doi: 10.1016/j.pec.2004.03.002. [DOI] [PubMed] [Google Scholar]
  • 157.Mattila R, Malmivaara A, Kastarinen M, Kivela SL, Nissinen A. Effectiveness of multidisciplinary lifestyle intervention for hypertension: a randomised controlled trial. J Hum Hypertens. 2003;17:199–205. doi: 10.1038/sj.jhh.1001531. [DOI] [PubMed] [Google Scholar]
  • 158.Maxwell A, Bastani R, Vida P, Warda U. Physical activity among older Filipino-American women. Women Health. 2002;36:67–79. doi: 10.1300/J013v36n01_05. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 159.Mayou R. A controlled trial of early rehabilitation after myocardial infarction. J Cardiopulm Rehabil. 1983;3:397–402. [Google Scholar]
  • 160.McGilley BM. Influence of exercise rehabilitation on coronary patients: a six-year follow-up evaluation [Dissertation] Lawrence, KS: University of Kansas; 1987. [Google Scholar]
  • 161.Mersebach H, Klose M, Svendsen O, Astrup A, Feldt-Rasmussen U. Combined dietary and pharmacological weight management in obese hypopituitary patients. Obes Res. 2004;12:1835–1843. doi: 10.1038/oby.2004.228. [DOI] [PubMed] [Google Scholar]
  • 162.Montgomery E, Lieberman A, Singh G, Fries J. Patient education and health promotion can be effective in Parkinson's disease: a randomized controlled trial. Am J Med. 1994;97:429–435. doi: 10.1016/0002-9343(94)90322-0. [DOI] [PubMed] [Google Scholar]
  • 163.Moore SM, Charvat JM. Using the CHANGE intervention to enhance long-term exercise. Nurs Clin North Am. 2002;37:273–283. doi: 10.1016/s0029-6465(01)00008-1. [DOI] [PubMed] [Google Scholar]
  • 164.Morrin L, Black S, Reid R. Impact of duration in a cardiac rehabilitation program on coronary risk profile and health-related quality of life outcomes. J Cardiopulm Rehabil. 2000;20:115–121. doi: 10.1097/00008483-200003000-00005. [DOI] [PubMed] [Google Scholar]
  • 165.Mostert S, Kesselring J. Effects of a short-term exercise training program on aerobic fitness, fatigue, health perception, and activity level of subjects with multiple sclerosis. Mult Scler. 2002;8:161–168. doi: 10.1191/1352458502ms779oa. [DOI] [PubMed] [Google Scholar]
  • 166.Murchie P, Campbell NC, Ritchie LD, Simplson JA, Thain J. Secondary prevention clinics for coronary heart disease: four year follow up of a randomized controlled trial in primary care. Br Med J. 2003;326:84–89. doi: 10.1136/bmj.326.7380.84. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 167.Neuberger GB, Smith KV, Black SO, Hassanein R. Promoting self-care in clients with arthritis. Arthritis Care Res. 1993;6:141–148. doi: 10.1002/art.1790060306. [DOI] [PubMed] [Google Scholar]
  • 168.Oh H, Seo W. Decreasing pain and depression in a health promotion program for people with rheumatoid arthritis. J Nurs Sch. 2003;35:127–132. doi: 10.1111/j.1547-5069.2003.00127.x. [DOI] [PubMed] [Google Scholar]
  • 169.Ornish D, Schewitz L, Billings J, Brown S, Gould K, Merritt T, Sparier S, Armstrong W, Ports T, Kirkeside R, Hogeboom C, Brand R. Intensive lifestyle changes for reversal of coronary heart diseases. JAMA. 1998;23:2001–2007. doi: 10.1001/jama.280.23.2001. [DOI] [PubMed] [Google Scholar]
  • 170.Painter P, Carlson L, Carey S, Paul S, Myll J. Physical functioning and health-related quality-of-life changes with exercise training in hemodialysis patients. Am J Kidney Dis. 2000;35:482–492. doi: 10.1016/s0272-6386(00)70202-2. [DOI] [PubMed] [Google Scholar]
  • 171.Painter Pl, Hector L, Ray K, Lynes L, Paul S, Dodd M, Tomlanovich S, Ascher N. Effects of exercise training in coronary heart disease risk factors in renal transplant recipients. Am J Kidney Dis. 2003;42:362–369. doi: 10.1016/s0272-6386(03)00673-5. [DOI] [PubMed] [Google Scholar]
  • 172.Penckofer S, Llewellyn J. Adherences to risk-factor instructions one year following coronary artery bypass surgery. J Cardiovasc Nurs. 1989;3:10–24. doi: 10.1097/00005082-198905000-00008. [DOI] [PubMed] [Google Scholar]
  • 173.Petrella RJ, Bartha C. Home based exercise therapy for older patients with knee osteoarthritis: a randomized clinical trial. J Rheumatol. 2000;27:2215–2221. [PubMed] [Google Scholar]
  • 174.Powell KW. Strategy to improve blood pressure control and medication adherence [Dissertation] Chicago, IL: Rush University; 2002. [Google Scholar]
  • 175.Prince R, Smith M, Dick I, Price R, Webb P, Henderson N, Harris M. Prevention of postmenopausal osteoporosis: a comparative study of exercise, calcium supplementation, and hormone-replacement therapy. N Engl J Med. 1991;325:1189–1195. doi: 10.1056/NEJM199110243251701. [DOI] [PubMed] [Google Scholar]
  • 176.Regensteiner JG, Steiner JF, Hiatt WR. Exercise training improves functional status in patients with peripheral arterial disease. J Vasc Surg. 1996;23:104–115. doi: 10.1016/s0741-5214(05)80040-0. [DOI] [PubMed] [Google Scholar]
  • 177.Rejeski W, Brawley L, Ambrosius W, Brubaker P, Focht B, Foy C, Fox L. Older adults with chronic disease: benefits of group-mediated counseling in the promotion of physically active lifestyles. Health Psychol. 2003;22:414–423. doi: 10.1037/0278-6133.22.4.414. [DOI] [PubMed] [Google Scholar]
  • 178.Riemsma RP, Taal E, Rasker JJ. Group education for patients with rheumatoid arthritis and their partners. Arthritis Care Res. 2003;49:556–566. doi: 10.1002/art.11207. [DOI] [PubMed] [Google Scholar]
  • 179.Rippey RM, Bill D, Abeles M, Day J, Downing DS, Pfeiffer CA, Thal S, Wetstone S. Computer-based patient education for older persons with osteoarthritis. Arthritis Rheum. 1987;30:932–935. doi: 10.1002/art.1780300814. [DOI] [PubMed] [Google Scholar]
  • 180.Rubin RR, Peyrot M, Saudek CD. Effect of diabetes education on self-care, metabolic control, and emotional well-being. Diabetes Care. 1989;10:673–679. doi: 10.2337/diacare.12.10.673. [DOI] [PubMed] [Google Scholar]
  • 181.Samaras K, Ashwell S, Mackintosh AM, Fleury AC, Campbell LV, Chisholm DJ. Will older sedentary people with non-insulin-dependent diabetes mellitus start exercising? A health promotion model. Diabetes Res Clin Pract. 1997;37:121–128. doi: 10.1016/s0168-8227(97)00061-2. [DOI] [PubMed] [Google Scholar]
  • 182.Sanderson CD. Functional capacity and adherence patterns in coronary patients participating in supervised versus unsupervised exercise training [Dissertation] Gainesville, FL: University of Florida; 1990. [Google Scholar]
  • 183.Scales R. Motivational interviewing and skills-based counseling in cardiac rehabilitation: the Cardiovascular Health Initiative and Lifestyle Education (Chile) study [Dissertation] Albuquerque, NM: University of New Mexico; 1998. [Google Scholar]
  • 184.Schaperclaus G, de Greef M, Rispens P, de Calonne D, Landsman M, Lie K. Participation in sports groups for patients with cardiac problems: an experimental study. Adapted Phys Act Q. 1997;14:275–284. [Google Scholar]
  • 185.Scholten C, Brodowicz T, Graninger W, Gardavsky I, Pils K, Pesau B, Eggl-Tyl E, Wanivenhaus A, Zielinski C. Persistent functional and social benefit 5 years after a multidisciplinary arthritis training program. Arch Phys Med Rehabil. 1999;80:1282–1287. doi: 10.1016/s0003-9993(99)90030-8. [DOI] [PubMed] [Google Scholar]
  • 186.Schuster PM, Wright C, Tomich P. Gender differences in the outcomes of participants in home programs compared to those in structured cardiac rehabilitation programs. Rehabil Nurs. 1995;20:93–101. doi: 10.1002/j.2048-7940.1995.tb01603.x. [DOI] [PubMed] [Google Scholar]
  • 187.Sharazand S, Canfield J, Kuschner W. Improved quality of life among patients completing a pulmonary rehabilitation program: one center's early experience. Respir Care. 2001;46:595–600. [PubMed] [Google Scholar]
  • 188.Singh RB, Rastogi V, Rastogi SS, Niaz MA, Beegom R. Effect of diet and moderate exercise on central obesity and associated disturbances, myocardial infarction and mortality in patients with and without coronary artery disease. J Am Coll Nutr. 1996;15:592–601. doi: 10.1080/07315724.1996.10718635. [DOI] [PubMed] [Google Scholar]
  • 189.Song R, Lee H. Effects of a 12-week cardiac rehabilitation exercise program on motivation and health-promoting lifestyle. Heart Lung. 2001;30:200–209. doi: 10.1067/mhl.2001.113282. [DOI] [PubMed] [Google Scholar]
  • 190.Southard BH, Southard DR, Nuckolls J. Clinical trial of an internet-based case management system for secondary prevention of heart disease. J Cardiopulm Rehabil. 2003;23:341–348. doi: 10.1097/00008483-200309000-00003. [DOI] [PubMed] [Google Scholar]
  • 191.Stanton JM, Arroll B. The effect of moderate exercise on mood in mildly hypertensive volunteers: a randomized controlled trial. J Psychosom Res. 1996;40:637–642. doi: 10.1016/0022-3999(95)00643-5. [DOI] [PubMed] [Google Scholar]
  • 192.Stenlund T, Lindstrom B, Granlund M, Burell G. Cardiac rehabilitation for the elderly: Qi Gong and group discussions. Eur J Cardiovasc Prev Rehabil. 2005;12:5–11. [PubMed] [Google Scholar]
  • 193.Stenstrom CH, Lindell B, Swanberg E, Swanberg P, Harms-Ringdahl K, Nordemar R. Intensive dynamic training in water for rheumatoid arthritis functional class II--a long-term study of effects. Scand J Rheumatol. 1991;20:358–365. doi: 10.3109/03009749109096812. [DOI] [PubMed] [Google Scholar]
  • 194.Sullivan T, Allegrante JP, Peterson MG, Kovar PA, MacKenzie C. One-year followup of patients with osteoarthritis of the knee who participated in a program of supervised fitness walking and supportive patient education. Arthritis Care Res. 1998;11:228–233. doi: 10.1002/art.1790110403. [DOI] [PubMed] [Google Scholar]
  • 195.Sward K. Effects of resistance exercise training on muscular strength, functional fitness, physical self-perception, and quality of life in the elderly [Dissertation] Pittsburgh, PA: University of Pittsburgh; 2001. [Google Scholar]
  • 196.Talbot LA, Gaines JM, Huynh TN, Metter EJ. A home-based pedometer-driven walking program to increase physical activity in older adults with osteoarthritis of the knee: a preliminary study. J Am Geriatr Soc. 2003;51:387–392. doi: 10.1046/j.1532-5415.2003.51113.x. [DOI] [PubMed] [Google Scholar]
  • 197.Tapanya S. A biopsychosocial intervention program to improve medical regimen adherence and glycemic control in type ll diabetic patients [Dissertation] New Brunswick, Canada: University of New Brunswick; 1996. [Google Scholar]
  • 198.Toda Y. The effect of energy restriction, walking, and exercise on lower extremity lean body mass in obese women with osteoarthritis of the knee. J Orthop Sci. 2001;6:148–154. doi: 10.1007/s007760100063. [DOI] [PubMed] [Google Scholar]
  • 199.Toobert DJ, Glasgow RE, Radcliffe JL. Physiologic and related behavioral outcomes from the Women's Lifestyle Heart Trial. Ann Behav Med. 2000;22:1–9. doi: 10.1007/BF02895162. [DOI] [PubMed] [Google Scholar]
  • 200.Trofimuk-Thomas G. The effectiveness of standardized vs individualized teaching, in combination with a counseling and exercise program, for clients in cardiac rehabilitation programs, in relation to the reduction of coronary risk factors [Dissertation] DeKalb, IL: Northern Illinois University; 1986. [Google Scholar]
  • 201.Tudor-Locke CE. Development, implementation and evaluation of a daily physical activity intervention for individuals with Type 2 diabetes [Dissertation] Ontario, Canada: University of Waterloo; 1999. [Google Scholar]
  • 202.Tudor-Locke C, Bell RC, Myers AM, Harris SB, Ecclestone NA, Lauzon N, Rodger NW. Controlled outcome evaluation of the First Step Program: a daily physical activity intervention for individuals with type II diabetes. Int J Obes Relat Metab Disord. 2004;28:113–119. doi: 10.1038/sj.ijo.0802485. [DOI] [PubMed] [Google Scholar]
  • 203.Van den Arend I, Stolk R, Rutten G, Schrijvers G. Education integrated into structured general practice care for Type 2 diabetic patients results in sustained improvement in disease knowledge and self-care. Diabet Med. 2000;17:190–197. doi: 10.1046/j.1464-5491.2000.00232.x. [DOI] [PubMed] [Google Scholar]
  • 204.van Elderen-van Kemenade T, Maes S, van den Broek Y. Effects of a health education programme with telephone follow-up during cardiac rehabilitation. Br J Clin Psycho. 1994;33:367–378. doi: 10.1111/j.2044-8260.1994.tb01133.x. [DOI] [PubMed] [Google Scholar]
  • 205.Vestfold Heartcare Study Group. Influence on lifestyle measures and five-year coronary risk by a comprehensive lifestyle intervention programme in patients with coronary heart disease. Eur J Cardiovasc Prev Rehabil. 2003;10:429–437. doi: 10.1097/01.hjr.0000107024.38316.6a. [DOI] [PubMed] [Google Scholar]
  • 206.Wallner S, Watzinger N, Lindschinger M, Smolle KH, Toplak H, Eber B, Dittrich P, Elmadfa I, Klein W, Krejs GJ, Wascher TC. Effects of intensified lifestyle modification on the need for further revascularization after coronary angioplasty. Eur Journal Clin Invest. 1999;29:372–379. doi: 10.1046/j.1365-2362.1999.00456.x. [DOI] [PubMed] [Google Scholar]
  • 207.Wdowik M, Kendall P, Harris M, Kelm K. Development and evaluation of an intervention program: control on campus. Diabetes Educ. 2000;26:95–104. doi: 10.1177/014572170002600110. [DOI] [PubMed] [Google Scholar]
  • 208.Welty FK, Stuart E, O'Meara M, Huddleston J. Effect of addition of exercise to therapeutic lifestyle changes diet in enabling women and men with coronary heart disease to reach Adult Treatment Panel III low-density lipoprotein cholesterol goal without lowering high-density lipoprotein cholesterol. Am J Cardiol. 2002;89:1201–1204. doi: 10.1016/s0002-9149(02)02305-6. [DOI] [PubMed] [Google Scholar]
  • 209.Whittemore R, Chase S, Mandle CL, Roy SC. The content, integrity, and efficacy of a nurse coaching intervention in type 2 diabetes. Diabetes Educ. 2001;27:887–898. doi: 10.1177/014572170102700614. [DOI] [PubMed] [Google Scholar]
  • 210.Wiggam J, French R, Henderson H. The effects of a token economy on distance walked by senior citizens in a retirement center. Am Correct Ther J. 1986;40:6–12. [Google Scholar]
  • 211.Willenheimer R, Rydberg E, Cline C, Broms K, Hillberger B, Oberg L, Erhardt L. Effects on quality of life, symptoms and daily activity 6 months after termination of an exercise training programme in heart failure patients. Int J Cardiol. 2001;77:25–31. doi: 10.1016/s0167-5273(00)00383-1. [DOI] [PubMed] [Google Scholar]
  • 212.Wing RR, Marcus M, Epstein L, Jawad A. A “Family-Based” approach to the treatment of obese type II diabetic patients. J Consult Clin Psychol. 1991;59:156–162. doi: 10.1037//0022-006x.59.1.156. [DOI] [PubMed] [Google Scholar]
  • 213.Wisnewski CA. A study of the health-promoting behavioral effects of an exercise educational intervention in adult diabetics [Dissertation] Denton, TX: Texas Woman's University; 1996. [Google Scholar]
  • 214.Worcester MU, Stojcevski Z, Murphy B, Goble AJ. Long-term behavioral outcomes after attendance at a secondary prevention clinic for cardiac patients. J Cardiopulm Rehabil. 2003;23:415–422. doi: 10.1097/00008483-200311000-00004. [DOI] [PubMed] [Google Scholar]
  • 215.Yates BC, Anderson T, Hertzog M, Ott C, Williams J. Effectiveness of follow-up booster sessions in improving physical status after cardiac rehabilitation: health, behavioral, and clinical outcomes. Appl Nurs Res. 2005;18:59–62. doi: 10.1016/j.apnr.2004.06.012. [DOI] [PubMed] [Google Scholar]
  • 216.Young DR, Appel LJ, Jee S, Miller E. The effects of aerobic exercise and Tai Chi on blood pressure in older people: results of a randomized trial. J Am Geriatr Soc. 1999;47:277–284. doi: 10.1111/j.1532-5415.1999.tb02989.x. [DOI] [PubMed] [Google Scholar]
  • 217.Young D, Kittke T, McCall M, Blume D. A prospective controlled study of in-hospital myocardial infarction rehabilitation. Journal of Cardiac Rehabilitation. 1982;2:32–40. [Google Scholar]
  • 218.Conn V, Hafdah A, LeMaster J, Ruppar T, Cochran J, Nielsen P. Interventions to improve self-management among adults with type 1 diabetes: Meta-analysis of metabolic outcomes. Am J Health Behav. doi: 10.5555/ajhb.2008.32.3.315. In press. [DOI] [PubMed] [Google Scholar]
  • 219.Conn V, Hafdahl A, Minor M, Nielsen P. Physical activity interventions among adults with arthritis: Meta-analysis of outcomes. Semin Arthritis Rheum. doi: 10.1016/j.semarthrit.2007.07.006. In press. [DOI] [PubMed] [Google Scholar]
  • 220.Conn V, Hafdahl A, Moore S, Nielsen P, Brown L. Meta-analysis of interventions to increase physical activity among adults with cardiovascular disease. Int J Cardiol. doi: 10.1016/j.ijcard.2008.03.052. In review. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 221.Vevea JL, Woods CM. Publication bias in research synthesis: Sensitivity analysis using a priori weight functions. Psychol Methods. 2005;10:428–43. doi: 10.1037/1082-989X.10.4.428. [DOI] [PubMed] [Google Scholar]
  • 222.Le Masurier GC, Sidman CL, Corbin CB. Accumulating 10,000 steps: does this meet current physical activity guidelines? Res Q Exercise Sport. 2003;74:389–94. doi: 10.1080/02701367.2003.10609109. [DOI] [PubMed] [Google Scholar]
  • 223.Tudor-Locke C, Bassett DR. How many steps/day are enough? Preliminary pedometer indices for public health. Sports Med. 2004;34:1–8. doi: 10.2165/00007256-200434010-00001. [DOI] [PubMed] [Google Scholar]
  • 224.Obarazanek E, Vollme WM, Lin PW, Cooper LS, Young DR, Ard JK, Stevens FJ, Simons-Morton DG, Svetkey LP, Harsha DW, Elmer PJ, Appel LJ. Effects of individual components of multiple behavior changes: The PREMIER trial. Am J Health Behav. 2007;31:545–560. doi: 10.5555/ajhb.2007.31.5.545. [DOI] [PubMed] [Google Scholar]
  • 225.Clark AM, Hartline L, Vandermeer B, McAlister FA. Quantitative synthesis documenting importance of secondary prevention. Ann Intern Med. 2005;143:659–72. doi: 10.7326/0003-4819-143-9-200511010-00010. [DOI] [PubMed] [Google Scholar]

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