Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2007 Jul 1.
Published in final edited form as: Diabetes Care. 2006 Jul;29(7):1656–1658. doi: 10.2337/dc06-0356

Should Group Education Classes Be Separated by Type of Diabetes?

Arlene Smaldone 1,2, Susan Lin 1, Om P Ganda 2,3, A Enrique Caballero 2,3, Sheila McMurrich 1, Katie Weinger 1,2, Keri Hannagan 1
PMCID: PMC1584305  NIHMSID: NIHMS12256  PMID: 16801595

Although the rising prevalence of type 2 diabetes and economic factors have resulted in more group diabetes education (1-4), little research has examined the effective use of group education or composition of groups. Regardless of group or individual education format, attention to individual learning needs through assessment of attitudes, health beliefs, motivation, and levels of self-care remain critical to tailoring programs to the adult learner. To maximize the benefit of the group format, educators must identify commonalities among group members to foster engagement and participation (5); however, this process can be difficult if participants vary in type of diabetes. In clinical practice, emphasis is typically on filling classes without attention to homogeneity; thus, assessing and addressing the needs of each group participant can be difficult (6). In this study, we examined whether adults with type 1 or type 2 diabetes requiring diabetes education differ in medical treatment issues, lifestyle, self-management, and psychosocial characteristics that may impact how they are educated in groups.

RESEARCH DESIGN AND METHODS

We evaluated the baseline data of 208 adults (type 1 diabetes, n = 101; type 2 diabetes, n = 107) enrolled in a longitudinal diabetes education study. The Committee on Human Subjects reviewed the study, and subjects provided informed written consent.

Subjects were eligible for the study if aged 18–75 years, if they had been diagnosed with type 1 or type 2 diabetes for ≥2 years, and if they had HbA1c (A1C) ≥7.6 and ≤14%. To be eligible, type 2 diabetic subjects needed to be treated with oral agents or insulin for at least 1 year. Exclusion criteria to prevent confounding factors and to maintain patient safety in the larger study included 1) initiation of intensive treatment within 6 months or current, or planning, pregnancy, as these may impact glycemia independent of diabetes education; and 2) presence of severe complication or comorbidity of diabetes that may place a person at risk when increasing physical activity (e.g., microalbuminuria, recent cardiovascular event, congestive heart failure, severe hypertension, eating disorder, unstable psychiatric disorder, or substance abuse).

We measured A1C, fasting lipid levels (unavailable for 20 of 101 type 1 diabetic participants), blood pressure, height, weight, and waist circumference. Subjects completed measures of frequency of self-care behaviors (Self-Care Inventory-Revised) (7), depressive symptoms (Brief Symptom Inventory 18) (8), diabetes-related emotional distress (Problem Areas in Diabetes) (9,10), diabetes quality of life (Diabetes Quality of Life Scale) (11,12), and coping styles (13). Subjects completed the 24-h food recall survey (14,15) and Seven-Day Physical Activity Recall (16,17), wore a pedometer for 3 days, and monitored glucose levels with study-provided meters and strips.

Data are presented as mean ± SD unless otherwise specified. All survey scores were converted to a 100-point scale for ease of interpretation (18). We used Nutritionist Pro to analyze food recall data and SAS 8.2 statistical software for data analysis.

RESULTS

Type 2 diabetic subjects were 1 decade older and had less formal education (Table 1). They had shorter diabetes duration and less intensive diabetes treatment regimens. Type 1 and type 2 diabetic participants were similar regarding depression (51.6 ± 10.3 vs. 50.8 ± 10.9), diabetes distress (39.3 ± 21.0 vs. 35.7 ± 19.3), and percent receiving anti-hypertensive therapy (38 vs. 45%). More type 2 diabetic subjects were treated for hyperlipidemia (46 vs. 32%; P = 0.04).

Table 1.

Sample characteristics for individuals with type 1 and type 2 diabetes

Type 1 diabetes Type 2 diabetes P value
n 101 107
Age (years)  44 ± 12.4  57 ± 9.2 <0.001
Diabetes duration (years)  24 ± 12.3  11 ± 7.8 <0.001
A1C (%) 9.0 ± 1.1   9.3 ± 1.3  NS
Blood pressure (mmHg)
  Systolic 121 ± 16.0  129 ± 13.4 <0.001
  Diastolic 73 ± 9.0  76 ± 8.7  0.01
Serum lipids (mg/dl)
  LDL cholesterol  99 ± 29.1  112 ± 33.5  0.01
  HDL cholesterol  63 ± 19.5   44 ± 12.1 <0.001
  Triglycerides  83 ± 47.8   161 ± 105.6 <0.001
BMI (kg/m2) 26.7 ± 5.0   32.6 ± 6.6  <0.001
Waist circumference (cm)
  Male 99.7 ± 13.2 110.0 ± 12.1 <0.001
  Female 83.5 ± 12.1 106.8 ± 18.2 <0.001
PAR metabolic expenditure (kcal/day) 2,483 ± 690   3,034 ± 650  <0.001
Pedometer (steps/day) 8,008 ± 3,781  5,491 ± 3,828 <0.001
Self-care
  Self-Care Inventory-Revised 56.7 ± 14.9 54.0 ± 16.4  NS
  Glucose monitoring (times per day) 3.5 ± 1.9 1.3 ± 1.1 <0.001
Psychosocial
  Coping styles
    Emotional 56.0 ± 13.9 48.2 ± 14.0 <0.001
    Self-controlled 65.4 ± 12.8 66.4 ± 12.2  NS
  Diabetes Quality of Life 63.6 ± 11.1 69.3 ± 10.3 <0.001
Sex (female) 63 (62) 47 (44)  0.008
Race/ethnicity  0.002
  Non-Hispanic white 96 (96) 81 (76)
  Non-Hispanic black 1 (1) 16 (15)
  Hispanic 2 (2) 5 (5)
  Asian, mixed, or other race 2 (2) 5 (5)
Education  0.02
  High school or less 17 (17) 34 (32)
  Some college 24 (24) 32 (30)
  College graduate or higher 60 (59) 41 (38)
Diabetes treatment regimen  0.001
  Oral medications 0 (0) 48 (46)
  NPH* 19 (19)  31 (29.5)
  Glargine* 58 (57) 25 (24)
  Insulin pump therapy 24 (24)  1 (0.5)
Treatment target goals met
  LDL cholesterol (n = 183) 43 (54) 44 (42) <0.001
  HDL cholesterol (n = 191) 76 (90) 50 (47) <0.001
  Triglyceride (n = 188) 73 (90) 60 (56) <0.001

Data are means ± SD or n (%) unless otherwise indicated.

*

May be combined with oral medications (type 2 diabetic subjects) or short-acting insulin (type 1 diabetic subjects).

LDL cholesterol <100 mg/dl on lipid-lowering agent or <130 mg/dl if not on lipid-lowing agent; HDL cholesterol >40 mg/dl male or >50 mg/dl female; triglycerides <150 mg/dl.

More type 1 diabetic subjects met blood pressure targets (19) (61 vs. 40%; P = 0.002). Fewer type 2 diabetic subjects met lipid treatment goals; they were also heavier and had larger waists. Type 2 diabetic participants reported lower daily calorie consumption and walked 2,500 fewer steps per day. However, they reported greater physical activity energy expenditure. Type 1 diabetic participants monitored blood glucose levels more frequently, reported poorer quality of life, and relied on emotional coping styles more frequently than type 2 diabetic participants.

CONCLUSIONS

The principle of extending education to many, while using limited resources, has driven the transition to group-based diabetes self-management education. This transition assumes homogeneity among participants, and individuals with diabetes do not necessarily fit into a homogenous group (20). We believe that discordance in patient characteristics and lifestyle behaviors minimizes the potential benefit of sharing experiences during group discussion. This discordance may force the educator to use a “one size fits all” educational approach (21). Our data suggest that adults with type 1 and type 2 diabetes differ along a wide range of characteristics and behaviors; these differences influence both participant learning requirements and educator's approach and strategy for teaching utilizing group process. Such differences in treatment regimens, cardiovascular risk, and lifestyle characteristics can negatively impact the success of education in facilitating lifestyle modification and treatment adherence (22).

Diabetes education focuses on self-care behavior, lifestyle issues, and understanding medications and prescriptions. Group education classes stimulate learning by allowing adults to incorporate their own experiences with diabetes into class discussion and, thus, actively engage in the learning process (5). To maximize the benefit of group education, participants must be able to relate to each other's shared experiences to inform or influence their own behavior (5).

Participants with type 2 diabetes reported lower caloric intake and higher physical activity levels, which are inconsistent with their much higher BMI, larger waist, and lower daily pedometer steps compared with type 1 diabetic subjects. The more objective measures (pedometer, BMI, and waist measurement) were consistent with the marked dyslipidemia and higher blood pressure found in the type 2 diabetic cohort. These reporting errors are consistent with prior research (23-25). Underreporting of caloric intake may be due to inattention to, or lack of knowledge of, healthy foods and portion size (26), both of which can negatively impact achievement of carbohydrate-counting proficiency. Overreporting of physical activity (23,24) may dampen motivation and impact strategies for setting and achieving goals. Both reporting errors may reflect the lack of awareness of their own lifestyle behaviors. Thus, in type 2 diabetic groups, awareness of one's behavior, basic healthy eating, and portion size activities may need to be a prerequisite before more sophisticated carbohydrate-counting activities can be meaningfully initiated. Different strategies for increasing physical activity may also be required. Setting physical activity goals as steps per day, rather than time spent exercising, may be more beneficial for those with type 2 diabetes (27). This study suggests that groups separated by type of diabetes may help participants when setting targeted, specific goals.

Our data support separating diabetes self-management education classes by type of diabetes to allow maximum benefit from group classes. Controlled trials are needed to further study this issue prospectively in order to provide evidence for defining high-quality diabetes education.

Acknowledgments

This work was supported by the National Institutes of Health (NIH) grant R01 DK60115 (to K.W.) and in part by NIH Research Resources M01 01032 to the Beth Israel Deaconess Medical Center and the Joslin Diabetes Center Satellite General Clinical Research Center, NIH Training Grant DK07260 (to A.S.), and the Diabetes and Endocrinology Research Core NIH P30 DK36836.

The following companies contributed glucose meters and test strips: Abbott Laboratories (Abbott Park, IL), LifeScan (Milpitas, CA), and Roche Diagnostics (Indianapolis, IN).

Footnotes

A.S. is currently an Assistant Professor of Nursing at Columbia University.

A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

References

  • 1.Rickheim PL, Weaver TW, Flader JL, Kendall DM. Assessment of group versus individual diabetes education: a randomized study. Diabetes Care. 2002;25:269–274. doi: 10.2337/diacare.25.2.269. [DOI] [PubMed] [Google Scholar]
  • 2.Plante WA, Lobato D, Engel R. Review of group interventions for pediatric chronic conditions. J Pediatr Psychol. 2001;26:435–453. doi: 10.1093/jpepsy/26.7.435. [DOI] [PubMed] [Google Scholar]
  • 3.Gary TL, Genkinger JM, Guallar E, Peyrot M, Brancati FL. Meta-analysis of randomized educational and behavioral interventions in type 2 diabetes. Diabetes Educ. 2003;29:488–501. doi: 10.1177/014572170302900313. [DOI] [PubMed] [Google Scholar]
  • 4.Roter DL, Hall JA, Merisca R, Nordstrom B, Cretin D, Svarstad B. Effectiveness of interventions to improve patient compliance: a meta-analysis. Med Care. 1998;36:1138–1161. doi: 10.1097/00005650-199808000-00004. [DOI] [PubMed] [Google Scholar]
  • 5.Zrebiec J. Tips for running a successful group. Diabetes Spectrum. 2003;16:108–110. [Google Scholar]
  • 6.Brown SA. Interventions to promote diabetes self-management: state of the science. Diabetes Educ. 1999;25:52–61. doi: 10.1177/014572179902500623. [DOI] [PubMed] [Google Scholar]
  • 7.Weinger K, Butler HA, Welch GW, La Greca AM. Measuring diabetes self-care: a psychometric analysis of the Self-Care Inventory-Revised with adults. Diabetes Care. 2005;28:1346–1352. doi: 10.2337/diacare.28.6.1346. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Derogatis LR, Melisaratos N. The Brief Symptom Inventory: an introductory report. Psychol Med. 1983;13:595–605. [PubMed] [Google Scholar]
  • 9.Welch GW, Jacobson AM, Polonsky WH. The Problem Areas in Diabetes Scale: an evaluation of its clinical utility. Diabetes Care. 1997;20:760–766. doi: 10.2337/diacare.20.5.760. [DOI] [PubMed] [Google Scholar]
  • 10.Polonsky WH, Anderson BJ, Lohrer PA, Welch G, Jacobson AM, Aponte JE, Schwartz CE. Assessment of diabetes-related distress. Diabetes Care. 1995;18:754–760. doi: 10.2337/diacare.18.6.754. [DOI] [PubMed] [Google Scholar]
  • 11.The DCCT Research Group Reliability and validity of a diabetes quality-of-life measure for the Diabetes Control and Complications Trial (DCCT) Diabetes Care. 1988;11:725–732. doi: 10.2337/diacare.11.9.725. [DOI] [PubMed] [Google Scholar]
  • 12.Jacobson AM, de Groot M, Samson JA. The evaluation of two measures of quality of life in patients with type I and type II diabetes. Diabetes Care. 1994;17:267–274. doi: 10.2337/diacare.17.4.267. [DOI] [PubMed] [Google Scholar]
  • 13.Peyrot M, McMurry JF, Jr, Kruger DF. A biopsychosocial model of glycemic control in diabetes: stress, coping and regimen adherence. J Health Soc Behav. 1999;40:141–158. [PubMed] [Google Scholar]
  • 14.Tippett K, Cypel Y. Design and Operation: The Continuing Survey of Food Intake by Individuals and the Diet and Health Knowledge Survey, 1994–1996. U.S. Department of Agriculture; Riverdale, MD: 1997. [Google Scholar]
  • 15.Ingwersen L, Anderson E, Tong A, Haggerty E, Anand J, Bodner J. USDA Food Instruction Booklet for CSFII 1994–96. U.S. Department of Agriculture; Riverdale, MD: 1998. [Google Scholar]
  • 16.Pereira MA, FitzerGerald SJ, Gregg EW, Joswiak ML, Ryan WJ, Suminski RR, Utter AC, Zmuda JM. A collection of physical activity questionnaires for health-related research. Med Sci Sports Exerc. 1997;29(Suppl 6):S1–S205. [PubMed] [Google Scholar]
  • 17.Blair SN, Applegate WB, Dunn AL, Ettinger WH, Haskell WL, King AC, Morgan TM, Shih JA, Simons-Morton DG. Activity Counseling Trial (ACT): rationale, design, and methods: Activity Counseling Trial Research Group. Med Sci Sports Exerc. 1998;30:1097–1106. doi: 10.1097/00005768-199807000-00012. [DOI] [PubMed] [Google Scholar]
  • 18.Trust M. How to Score the SF-36 Health Survey. Medical Outcomes Trust; Boston, MA: 1993. [Google Scholar]
  • 19.Chobanian AV, Bakris GL, Black HR, Cushman WC, Green LA, Izzo JL, Jr, Jones DW, Materson BJ, Oparil S, Wright JT, Jr, Roccella EJ, National Heart, Lung, and Blood Institute Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure, the National High Blood Pressure Education Program Coordinating Committee The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure: the JNC 7 report. JAMA. 2003;289:2560–2572. doi: 10.1001/jama.289.19.2560. [DOI] [PubMed] [Google Scholar]
  • 20.Funnell MM, Anderson RM, Austin A, Gillespie SJ. Individualization of diabetes self-management education. Diabetes Educ. 2002;28:741–745. doi: 10.1177/014572170202800515. 749. [DOI] [PubMed] [Google Scholar]
  • 21.Mensing C, Norris SL. Group education in diabetes: effectiveness and implementation. Diabetes Spectrum. 2003;16:96–103. [Google Scholar]
  • 22.Lacey KO, Chyun DA, Grey M. An integrative literature review of cardiac risk factor management in diabetes education interventions. Diabetes Educ. 2000;26:812–820. doi: 10.1177/014572170002600510. [DOI] [PubMed] [Google Scholar]
  • 23.Walsh MC, Hunter GR, Sirikul B, Gower BA. Comparison of self-reported with objectively assessed energy expenditure in black and white women before and after weight loss. Am J Clin Nutr. 2004;79:1013–1019. doi: 10.1093/ajcn/79.6.1013. [DOI] [PubMed] [Google Scholar]
  • 24.Lichtman SW, Pisarska K, Berman ER, Pestone M, Dowling H, Offenbacher E, Weisel H, Heshka S, Matthews DE, Heymsfield SB. Discrepancy between self-reported and actual caloric intake and exercise in obese subjects. N Engl J Med. 1992;327:1893–1898. doi: 10.1056/NEJM199212313272701. [DOI] [PubMed] [Google Scholar]
  • 25.Duncan GE, Sydeman SJ, Perri MG, Limacher MC, Martin AD. Can sedentary adults accurately recall the intensity of their physical activity? Prev Med. 2001;33:18–26. doi: 10.1006/pmed.2001.0847. [DOI] [PubMed] [Google Scholar]
  • 26.Black AE, Prentice AM, Goldberg GR, Jebb SA, Bingham SA, Livingstone MB, Coward WA. Measurements of total energy expenditure provide insights into the validity of dietary measurements of energy intake. J Am Diet Assoc. 1993;93:572–579. doi: 10.1016/0002-8223(93)91820-g. [DOI] [PubMed] [Google Scholar]
  • 27.Bjorgaas M, Vik JT, Saeterhaug A, Langlo L, Sakshaug T, Mohus RM, Grill V. Relationship between pedometer-registered activity, aerobic capacity and self-reported activity and fitness in patients with type 2 diabetes. Diabetes Obes Metab. 2005;7:737–744. doi: 10.1111/j.1463-1326.2004.00464.x. [DOI] [PubMed] [Google Scholar]
  • 28.Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol In Adults: Executive summary of the Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III) JAMA. 2001;285:2486–2497. doi: 10.1001/jama.285.19.2486. [DOI] [PubMed] [Google Scholar]

RESOURCES