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Published in final edited form as: Nurs Clin North Am. 2011 Dec 14;47(1):81–96. doi: 10.1016/j.cnur.2011.10.013

Community-Based Participatory Research and Smoking Cessation Interventions: A Review of the Evidence

Jeannette O Andrews 1,, Susan D Newman 2, Janie Heath 3, Lovoria B Williams 4, Martha S Tingen 5
PMCID: PMC3269631  NIHMSID: NIHMS333959  PMID: 22289400

SYNOPSIS

This article presents a review of the evidence on the use of community-based participatory research (CBPR) and smoking cessation interventions. An overview of CBPR is provided, along with a description of the search methods and quality scoring. Research questions are explored to determine: if CBPR improves the quality of research methods and community involvement in cessation intervention studies; and, cessation outcomes when using CBPR approaches. Results of the review are provided along with a comprehensive table summarizing all included studies. Strengths and challenges of the CBPR approach are presented with recommendations for future research.

Keywords: Smoking cessation, tobacco cessation, community-based participatory research, action research, participatory research


The Public Health Service (PHS) Guideline, Treating Tobacco Use and Dependence: 2008 Update [1], provides recommendations for tobacco cessation interventions for smokers in clinical and healthcare settings. Although tobacco cessation interventions delivered to marginalized populations in community settings have increased in the past decade, the effectiveness of novel community-based approaches is still unknown [1]. Over the past decade, one of these novel approaches, community-based participatory research (CBPR), has increasingly received credibility as a promising approach to address disparities in health outcomes in marginalized communities.

CBPR is a partnership approach to scientific inquiry that involves collaboration among community members, community partners and academic researchers throughout the research process [2]. CBPR strives for maximum feasible community participation on a continuum [3], including identifying issues to be addressed, design and delivery of interventions, evaluation of data, and dissemination of results [4,5]. Principally, as an orientation to research, CBPR can be incorporated with any research design, from descriptive studies to randomized controlled trials [3]. Compared to traditional research that is driven by academic investigators, CBPR offers the potential to improve intervention design and implementation, facilitates participant recruitment and retention, increases the quality and validity of the research, enhances the use and relevance of data, increase the rate of knowledge translation, and creates a shorter loop between research activity and community adoption of evidence-based practices [6,7].

Despite the lauded benefits and increased utilization of CBPR, there are only a few systematic reviews assessing the evidence of this approach, and none to date that have examined the evidence of CBPR and tobacco cessation interventions. The purpose of this paper is to review the relevant literature on the use, quality, and effectiveness of CBPR for smoking cessation interventions. The following research questions guided this integrative review:

  1. What is the evidence that a CBPR approach improves quality of research methodology and community involvement?

  2. What are the cessation outcomes of CBPR developed smoking cessation interventions?

Methods

An integrative review [8] was conducted using the following databases: Pub Med, Medline (OVID), PyscINFO, and Cumulative Index of Nursing and Allied Health Literature (CINAHL) from the dates January 1995 to June 2011. The following search terms were used: “smoking” or “smoking cessation” or “tobacco” or “tobacco cessation” AND “community based participatory research” or “action research” or “participatory research” or “academic-community partnerships” or “institutional community partnerships”. Search terms were determined after reviewing existing CBPR literature and compiling associated key words and subject headings. Reference lists were also searched of included studies for articles published that were not revealed in the initial search and for additional papers by the included authors for other supportive documents of the CBPR processes.

The following inclusion and exclusion criteria were used:

  • Inclusion Criteria
    1. smoking or tobacco cessation intervention;
    2. data-based studies with cessation outcomes reported;
    3. community partner identified; and
    4. description of community-partner involvement in the planning and/or execution of research.
  • Exclusion Criteria
    1. paper not available in English;
    2. tobacco prevention studies; or
    3. descriptive papers only with lack of reported cessation outcomes

Data Collection and Analyses

Two authors (JOA, SDN) independently reviewed the abstracts and articles for inclusion with 100% inter-rater reliability. Data extraction was conducted by using a standardized template developed by the research team to capture all relevant data. The template was reviewed by all members of the research team and consensus reached by discussion of team members.

Quality Scoring

The quality of the community participation and research methodology was scored using information available in the published articles. The tools used for quality scoring were originally developed by Viswanathan and colleagues [5] and adapted by Chen and colleagues [9]. The tool for quality of community participation [9] had two major domains: 1) nature of community involvement (selection of research questions, proposal development, financial responsibility for grant funds, study design, recruitment and retention of study participants, measurement instruments and data collection, intervention development and implementation, interpretation of findings, dissemination of findings, and application of findings to health concern identified); and, 2) evidence of community-based research elements (structure or mechanism for shared decision making, study designed to remove barriers to community participation, assessed social determinants of health (SDOH); addressed SDOH through design, research team flexibility, individual capacity building, community capacity building, dissemination to participants, application to health related intervention or policy change, and sustainability). Each item of the tool was scored from 1in (insufficient information), 1p (poor), 2 (fair) or 3 (good). Scores were summed and averaged, with possible scores ranging from 1–3, with higher scores indicating higher community involvement [9].

The tool [9] to score the quality of research methodology had 9 domains: research question, study population and external validity, control/comparison group, intervention/exposure, internal validity/fidelity, primary outcome measures, statistical analyses, blinding, and funding source. Scoring for this tool was the same as the quality tool described above, with possible scores ranging from 1–3, with higher scores representing higher quality and research rigor [9].

Search Results

A total of 247 abstracts were identified from the initial review. Of these, 108 were duplicates, and 122 did not meet the inclusion criteria, resulting in 17 papers for review. An additional hand search was conducted of reference lists with these included papers, yielding six additional papers, for a total of 23 papers, which described 11 cessation studies and associated CBPR partnerships.

Study Findings

Of the 11 studies, eight of these were cessation interventions targeted to adults and three to adolescents/young adults – see Table 1. All 11 studies were developed with a marginalized community. Two studies engaged partnerships with low socioeconomic African American communities [1015], three with Asian communities [1622], two with American Indian communities [2325], and one with a Native Hawaiian community [2628].

Table 1.

Summary of Studies Included in Review

Reference/
*Major
Paper
Purpose Community
Partners
Sample/Setting Approach/Design Intervention Cessation Outcomes Quality
Comm.
Involvement
Quality
Research
Comments
Andrews
et al.,
2005 [10]

Andrews
et al.,
2007 [11]

*Andrews
et al.,
2007 [12]

Andrews
et al.,
2011 [13]
Develop,
implement,
evaluate
cessation
intervention
in public
housing

“Sister to
Sister “
Housing
Authority;
Advisory
CAB
Board;
Lay
members
N=103
AA women

Setting:
2 public
housing
neighbor-
hoods
in
Southeast
US
- Described
partnership
development

- Intervention
development:
Focus groups,
key informant
interviews,
grounded theory
study,
quantitative
surveys

Design: Quasi-
experimental
with 2 groups
Multi-level
intervention:
-Community
health worker 1:
interaction weekly
× 12 weeks
- Group
counseling via
nurse × 6 weeks
- Nicotine patches
× 6 weeks
- Neighborhood
activities/policy

CL:
Written cessation
materials at
baseline and
group attention
weekly × 6 weeks
- 6 mo cessation
27.5% TX vs. 5.7%
CL (OR= 6.1–23.1)

- 7 day point
prevalence @ wk
12, 24 =
49%, 39%,39% in
vs. 15.%,7.6%,
11.5% CL

-validated via CO
2.8 2.6 -Met 100% recruitment
goals

-6 month retention rate:
87.5%

-Neighborhood level
policies

-Randomized cluster
design being conducted
in 14 neighborhoods in 2
states; n=406 women
*Bryce et
al., 2009
[29]
Develop,
implement,
evaluate a
midwife
intervention
to assist
pregnant
women and
partners to
quit
smoking

“Community
Action
on
Tobacco
for
Children’s
Health
(CATCH) “
Local
health
board;
midwife;
steering
group.
N=79
(65 women
14 male
partners)
Low SES
pregnant
smokers ≤
25 yrs and
partners

Setting:
Hospital
maternity
unit in West
Scotland
-Described
partnerships

-Needs
assessment
conducted;
training

Design:
Descriptive
study with 1
group
- Motivational
interviewing by
nurse midwife;
- Multiple
modalities offered
(1:1, couple, or
group)
- NRT;
- Home follow-up

(Duration of
intervention not
clear)
-3 mo cessation=
20.3%
-12 mo cessation =
12.7%

-validated by CO
1.65 1.5 -289 smokers eligible
(recruitment goals
unclear)

-88% retention at 3 mo

-47% retention at 12 mo
Burton et
al., 2004
[21]

*Shelly et
al.,2008
[22]
Estimate
the effect
of a
tailored
multicompo
nent
community-
based
smoking
cessation
intervention
within
context of
state and
city-wide
tobacco
control
initiatives
Community
based
organizations;
CAB
N= 2537
adults in
baseline
interview
(pre-test);
1384 from
original
cohort
completed
2nd interview
Chinese
immigrants
living in New
York City:
(post-test)

Setting:
TX
Community:
Flushing,
Queen, NY

CO
Community:
Sunset Park,
Brooklyn,
NY
-Household
interviews,
focus groups
prompt
mobilization

Design:
Pre-test, post-test
quasi-experimental
-Both communities
exposed to
tobacco control
public policy
changes over 2
year period (10-03
to 9-05)
-However, only
Flushing received
additional
linguistically and
culturally-specific
community-level
tobacco control
interventions
(public education,
social marketing,
posters,
brochures; acess
to language
specific cessation
resources)
-From 2002 to 2006
overall smoking
prevalence among
Chinese immigrants
declined from 17.7%
to 13.6% (relative
23% decrease)

-After controlling for
socio-demographic
characteristics, there
was an absolute
3.3% decrease in
smoking prevalence
attributed to policy
changes with an
additional absolute
decline in prevalence
of 2.8% in the
intervention
community relative to
the control
community

-Self report
2.0 2.4 -City wide policies

-Sustainable
Braun et
al., 2006
[26]

Braun et
al., 2006
[27]

*Santos
et al.,
2008
[28]
Test effect
of a
compre-
hensive
tobacco
cessation
protocol
that has
been
institutiona
lized in 5
Native
Hawaiian
Health
Care
Systems
(NHHCS)
Imi Hale-
Native
Hawaiian
Cancer
Network
represent
atives;
commun-
ity
outreach
workers;
Depart-
ment
of
Health;
others
-Clinics
developed
list of all
smokers in
past 6
months in 5
settings;
randomly
selected 30
charts at
each site for
review

Setting:
Five Native
Hawaiian
Health Care
Systems
(NHHCS)
-Described
partnership
development;
-Intervention
development;
statewide
surveys,
inventory
cessation
services;
groups,
interviews

Design:
Observational
-Culturally tailored
AHRQ protocols
for smoking
cessation in 5
health systems

-Offered brief,
intensive, and
systems
interventions
based on 5As.
-80%- 100% of
NHHCs clients asked
about tobacco use

-57%-100% clients
received brief
intervention

-21/50 (42%) clients
completing
intervention remained
abstinent at 3 months
-self report
2.1 1.7 -Varying levels of
adoption of intervention
at 5 sites

-6 years to develop
protocol

-System changes yield
likelihood of
sustainability
*Daley et
al., 2010
[23]
Develop,
implement,
evaluate
pilot
culturally
tailored
cessation
intervention
in urban
and
reservation
communities

“All Nations
Breath of
Life”
Native
American
commun-
ity
members
N=108
Native
American
adult
smokers

Setting:
Urban and
reservation
Native
American
communities
in Kansas
-Described
intervention
development:
-Focus groups;
pilot testing with
4 iterations of
the program;
Intervention
testing

Design:
Descriptive with
one group.
Intervention has 5
components:
-Group support
weekly × 9 groups
-Individual phone
counseling with
motivational
interviewing × 12
weeks
-educational
curriculum
-pharmacotherapy
(participant
choice)
-participant
incentives
-65% cessation at
program completion

- 6 mo cessation =
25%

-Self report
1.8 1.4 - Recruitment
target/eligibility unknown

-No retention rates
reported
*Froelicher
et al.,
2010
[14]

Malone et
al., 2006
[15]
Investigate
whether
tobacco
industry
documents
in a
cessation
program
contextuali
ze the
social
justice
implication
s of
tobacco
promotion
could
assist AA
quit
smoking

“Protecting
the hood
against
tobacco
(PHAT)”
San
Francisco
African
American
Tobacco
Free
Project;
and the
Bayview
and
Hunter's
Point
neighborhoods
N=60 AA
smokers

Setting:
Public clinic
adjacent to
large AA
neighbor-
hood
in San
Francisco
-Intervention
development
included focus
groups, town
hall meetings,
community
survey

Design:
RCT
TX: 5 week
intervention
program plus
tailored tobacco
industry and
media messages
(i.e., to reinforce
tobacco industry
targeting,
community
empowerment,
and social justice)
plus phone
support; NRT
available

CL: standard 5
week cessation
intervention, NRT
available
-6 mo cessation =
13.6% TX vs 11.5 CL

- 12 mo cessation =
15.8 TX vs 5.3 CL

-Validated by salivary
cotinine
1.55 2.2 -Recruitment goal= 270
participants

-Difficulty with
recruitment

-37% retention at 12 mo
*Horn et
al., 2005
[24]

Horn et
al., 2008
[25]
Test an
adapted
American
Lung
Association
program for
American
Indian
Teen
Cessation

“American
Indian Not
On
Tobacco
Program;
AINOT”
Tribal
partner
organizat
ion, other
local,
state,
national
partners;
CAB
N=74
(54 TX and
20 CO)
American
Indian
smokers 14–19 years old

Setting:
North
Carolina
American
Indian
community;
10 schools
-Described
partnership
development;
-Demonstrated
CBPR principles
throughout
study

Design:
Quasi-
experimental
with 2 groups
AI NOT
Intervention:
10 sessions, I hr
per week, up to 4
booster sessions
over 3 months in
group setting

CL: Brief
intervention (15
minute classroom
session)
- 3 mo cessation:
ITT18% TX vs. 10%
CO) (NS)

-28.6% males (n=6)
in TX vs. 14.3% (n=1)
males in CL reported
cessation; no females
reported cessation

-Self report
3 2.3 -Recruitment goal =200
youths;

-Challenge to recruit
expected sample in time
frame

-58% retention rates
Ma et al.,
2004 [16]

Ma et al.,
2005 [17]

Ma et al.,
2006 [18]

*Wu et
al., 2009
[19]
Develop
and test
culturally
tailored
smoking
cessation
for Chinese
American
Smokers
Asian
Tobacco
Educa-
tion
and
Cancer
Aware-
ness
Research
Special
Popula-
tion
Network;
Asian
Community
Health
Coalition
N=122 Asian
American
smokers

Setting:
New York
City
-Described
partnership
formation
-Feasibility
testing
-Comprehensive
CBPR model

Design:
Experimental;
pre-post test
design with 2
groups
-TX: 4
individualized
counselor led
motivational
interviewing
sessions and NRT

-CL: 4 health
education groups
-6 mo cessation
67% TX vs. 32% CL

-validated by CO
3.0 2.7 - Met recruitment goals

-88% retention at 6
months

-Planning larger RCT
*McDonnell
et al.,
2011
[20]
Develop,
implement,
and
evaluate
online
cessation
program
tailored for
Korean
Americans
“Quitting is
Winning”
Korean
CAB in
California
N=1112
Korean
American
smokers;
88% men

Setting:
Recruited
via ads in
major
newspapers
and
websites in
the Korean
American
Community
in US
-Described
partnership
formation
-Conducted in-
depth
interviews;
-Intervention
development

Design:
RCT
TX: Online self
help based on
Stop Smoking
Center program;
cognitive
behavioral self -
help program
based on stages
of change with 6
sections
CL: mailed booklet
version of online
program;
Both materials
translated into
Korean
-At 50 weeks, no
difference in 30-day
cessation between
the internet group
(11%) vs. booklet
(13%)

-Quitting was higher
among participants in
intervention group
who completed the
online program (26%
vs. 10%) who did not
complete

-self report
1.7 2.6 - 2 ½ year recruitment
period

-48% completed
assessments in TX and
57% in CL
Mendenhall
et al.,
2008 [31]

*Mendenhall
et al.,
2010
[32]
Develop,
implement
and test an
intervention
that
engages
local media
and
providers
to reduce
on-campus
smoking at
Job Corp

“Students
against
Nicotine
and
Tobacco
Addition
SANTA”
Students,
teachers,
and
administ-
rators
in
Minnie-
polis/
St
Paul Job
Corps
200–250
students on
campus on
average,
with 6–18 mo
residency;
40% smoke

Setting:
Job Corp
Campus in
Minneapolis/
St Paul
.
-Described
partnership
development;
-Intervention
development:
surveys, focus
groups;
Implementation
of system wide
changes

Design:
Cross-sectional
with prevalence
surveys every 3
months
Several system
wide changes on
campus involving:
1) fighting stress
and boredom
(alternative
activities)
2) changing
physical
environment
3) changing
policies
4) revising
smoking cessation
education and
support
-No change in overall
smoking prevalence
on campus
-Increasing number
of students report
smoking less
cigarettes per day
(p < .018)

-Self report
2.4 1.5 -Policy changes
- Sustainable beyond
grant funding
*Woodruff
et al.,
2007
[30]
Test
internet
based teen
cessation
intervention

“Breathing
room
study”
School
partners
N= 136 teen
smokers

Setting:
14 high
schools
randomized
to TX or CL
in San Diego
county
-Partnership
development;
-Contributions to
recruitment,
study design,
materials

Design:
Randomized
cluster design (7
schools per
condition);
analyses by
individuals
TX: Seven 45-
minute Internet
based, virtual
reality world
combined with
motivational
interviewing over
7-week period

CL: Measurement
only
-TX participants were
more likely to report
abstinence during
past week
immediately post
intervention (35% vs.
22% P < .01), yet no
differences at 12
months (38% vs.
29%).
-Only number of
times quit was
significant at 12
months (2.4 vs. 1.7, p
< .05)
-Self report
2.4 2.5 - Target recruitment
unknown; 300 students
showed interest, 200
eligible

-73% retained

CL = Control

CO = Comparison

NRT = Nicotine Replacement Therapy

CAB= Community Advisory Board

ITT= Intent to treat

RCT = Randomized Controlled Trial

Several studies used a CBPR approach to socio-culturally tailor the PHS Guidelines for individuals utilizing both behavioral counseling and pharmacotherapeutics [1019, 23, 29]. Shelley and colleagues [21, 22] evaluated the effect of community-wide policy changes on cessation, in addition to a cadre of PHS based cessation programs and resources in the treatment community. Froelicher and colleagues [14, 15] enhanced their 5-week PHS guided intervention (i.e., counseling, nicotine replacement therapy) with tailored tobacco industry and media messages to reinforce tobacco industry targeting to the African American community. Santos and colleagues [2628] implemented PHS recommendations for system level changes (i.e., 5 As - Ask, Advise, Assess, Assist, Arrange) in five health systems. Two studies used a CBPR approach to develop an internet-based cessation intervention: one for teens in school systems [30] and the other a tailored internet-based cessation for a national sample of Korean Americans [20].

Research Question #1: What is the evidence that a CBPR approach improves quality of community involvement and research methodology?

As guided by the inclusion criteria, all studies included academic or clinical investigators and community partners. Further, an advisory board or steering committee guided all intervention studies. It was evident in several studies that the original question and need for the tobacco cessation intervention originated from the community [1015, 20, 2325, 31,32]. In other studies, the origination was either unknown and/or originated from the academic or clinical partner. The partnerships were utilized to conduct needs assessment surveys (quantitative and/or qualitative) [1015, 21, 22, 29, 31, 32], intervention development [1019, 20, 2123, 2628, 3032], recruitment of participants (1028,3032], intervention delivery [1019, 2128, 31, 32], evaluation [1013, 1619, 2428,31,32], and dissemination [1013, 1619, 24, 25, 31,32].

The quality of community involvement varied, with quality scores ranging from 1.5 to 3 (highest score possible was 3). Those with lower community involvement scores tended to have challenges with participant recruitment and retention [14, 15, 29]. An exception was the study conducted by Horn and colleagues [24, 25] that tested a cessation intervention for Native American teens in school settings, and demonstrated high community involvement throughout the process (scored 3/3), yet only recruited 39% of the intended sample.

The studies with higher community scores were more likely to involve the community with dissemination [1013, 1619, 24, 25, 31, 32]. Dissemination in community settings was typically town hall forums or community meetings or workshops, advisory or steering groups, newsletters, and local media. Several studies implemented policy changes in the targeted setting [1013, 21, 22, 2628, 31, 32], which potentially may increase the likelihood of sustainability. Two of these authors [24, 25, 31, 32] described sustainability of the intervention post initial grant funding, as a result of leadership, systems and/or environmental changes, and governing infrastructures.

The quality of the research methodology varied, with quality scores ranging from 1.4 to 2.7. The seven studies with quasi-experimental or experimental designs [1022, 24, 25, 30] scored 2.2 or higher. The remaining four studies were descriptive or observational studies with one group only [2123, 29, 31, 32]. Eight studies measured abstinence rates at six months or longer [1023, 29, 30], yet four of these eight studies [2023, 30] did not biochemically validate self-report outcomes.

Research Question #2: What are the cessation outcomes of CBPR developed smoking cessation interventions?

As shown in Table 1, the cessation outcomes varied by study design, Intervention dosages and intensity, intervention content and delivery, study goals, resources, and duration. The two studies that scored 2.5 or higher quality scores for both quality in community involvement and research rigor demonstrated significant treatment outcomes for the six-month cessation compared to the control condition. For example, Wu and colleagues [1619] partnered with the Asian Community Health Coalition in New York City, which was part of the larger Asian Tobacco Education and Cancer Awareness Research (ATECAR) Special Population Network [18]. A series of formative studies were conducted, with the team revising the study design and implementation over time, leading to the development of an intervention with tailored motivational interviewing counseling sessions, packet of self-help materials, and nicotine replacement therapy (NRT). The investigators worked with the coalition and community members to tailor the intervention to meet the cultural and linguistic needs of the Chinese American community. The 7-day point prevalence abstinence at six months was 67% in the treatment condition compared to 32% in the control condition [19].

Similarly, Andrews and colleagues [1013] partnered with public housing officials and residents to develop a multi-level cessation intervention for African American women (i.e., Sister to Sister) in public housing neighborhoods. The original interest for the intervention was generated by a community partner, and over time, the partners developed an intervention with four major components: neighborhood-level component (two anti-smoking activities and one policy change); peer groups (behavioral counseling); 1:1 coaching sessions by community health workers; and NRT. The 7-day point prevalence abstinence at six months was 39% in the treatment condition compared to 11.5% in the control condition [12]. It is noteworthy that both of these studies adapted the PHS Guideline recommendations for the engaged community, as well as incorporated the local context of the community to develop and implement the intervention. Both of these studies were considered pilot studies for larger randomized trials, and based on these pilot data the Sister to Sister Intervention is currently being tested in a larger trial in 16 neighborhoods (NIH Grant # 5 R01HL090951-03, PI: J. Andrews).

Discussion

The review highlights several strengths of utilizing a CBPR approach and engaging with communities to develop, implement and evaluate smoking cessation interventions. First, a CBPR approach can be used by interprofessional academicians and diverse community partners to develop smoking cessation interventions with marginalized communities. CBPR can be effective in enhancing community input, building community capacity, and addressing barriers to health in study participants who have historically been underrepresented in research [33]. A CBPR approach with high levels of community involvement, as highlighted in this review, has been used successfully to partner with communities to conduct needs assessment surveys, develop interventions, recruit participants, deliver interventions, evaluate, and disseminate interventions. All studies included in this review had evidence of a community advisory or steering board to guide the processes of the research.

Another strength highlighted in this review, is that CBPR assists with the external validity challenges of traditional translational research, or translating specific findings from highly controlled trials to real world community interventions [4]. The majority of the studies in this review based their cessation interventions on the PHS Guideline recommendations, yet delivered these evidence-based modalities within diverse contexts, and situated the intervention within cultural, environmental, and community factors. While the academic partners contributed expertise on the PHS Guideline and evidence-based approaches to cessation, the community partners contributed expertise on the local context applicable to the community. Further, as suggested by others [34], the complexity of interactions between the structure, processes, and goals of the intervention and those of the community itself, arise from and are strengthened by the knowledge of the community. This unique type of partnership, blend of expertise, and knowledge generation helps to transcend some of these challenges in translating evidence-based interventions into complex community settings [2, 33].

One of the major goals of CBPR is to enhance collective action for change [1], and several papers demonstrated evidence of systems level and/or policy change in the engaged community practice or community setting. Systems level changes and policy changes are more likely to be sustained over time, as compared to traditional research that often ends once grant funding is over. The involvement and mobilization of community members from the onset, and working through the complexities of institutionalization and sustainability of a health promoting intervention, are likely to foster community empowerment and social action over time [3538]. Ideally, empowerment is both a process and an outcome of CBPR [39].

Besides highlighting strengths, this review also highlights several challenges of using CBPR. First, CBPR is utilized in varying degrees of the established principles of “ideal CBPR” frequently reported by Israel and colleagues [2]. For example, one of the major principles of CBPR is that the community is involved with all phases of the research process. However, there was evidence that the original research question was derived from the community in only six of the 11 studies. Less than half of the studies documented the community’s involvement with dissemination and even fewer discussed plans for sustainability of the intervention. As others report, [38] adherence to the ideal CBPR model is very challenging for these partnerships. The process of defining the community itself can be complex, whether it may be from a small geographically defined community that may be too small to adequately recruit participants for a clinical trial, in contrast to a community that is diffuse and larger, making it difficult to establish meaningful and representative partnerships [38].

Another challenge highlighted by the Froelicher study [14, 15] in this review and others in the literature [3, 38, 40] is the navigation of the Institutional Review Board (IRB) process for community-based studies. Navigating the IRB for CBPR studies is often time consuming. Either a lack of understanding and/or differing interpretations of the institutional and federal IRB regulations by IRB administrators and investigators may impede the process. There remains controversy about appropriate criteria for evaluating CBPR proposals and the associated ethical implications [3]. Until these controversies are resolved and consensus is reached, this area will likely remain a challenge for CBPR partnerships.

The time involved in developing relationships, building trust, and sustaining intervention effects is another frequently documented challenge in the conduct of CBPR [2, 4, 6, 7, 36, 39] and as noted in this review. Partnerships may take several years to develop, the development and feasibility testing of interventions take considerable time with these unique partnerships, which then is compounded with the challenges to sustain grant funding or other financial resources over many years. Several partnerships in this review had weathered this process and demonstrated a 10-year or longer relationship [1013, 1619]. However, the time factor can be problematic on many fronts, especially for the junior investigator attempting promotion and tenure status, changes in leadership in both the academic and community setting, and other transitions and unforeseen obstacles that may occur [13, 38]. This can be especially difficult in marginalized communities where both residents and involved partnering organizations may be transitory [13].

This review highlights the challenge of maintaining the rigor of academic preferred research designs (i.e., randomized controlled trials) and the “dance” of incorporating community preferences, which typically do not involve research, but rather services and programs in the community [4, 36, 38]. Seven of the 11 studies incorporated a quasi-experimental or experimental design, yet only three of these seven met other commonly accepted cessation treatment outcome criteria of reporting at least 6-month abstinence rates that are biochemically verified [41,42]. Increasingly, investigators support the practice that experimental designs may not always be feasible or appropriate to adequately test the effectiveness of community-based interventions [3, 34]. For example, observational studies, as utilized by four of the included studies in this review, are becoming increasingly recognized as a practical and ethical alternative to randomized controlled trials that allows for strong causal inference [34, 43, 44].

Community interventions are complex interactions, expensive, and labor intensive. Although this review did not assess the funding level for these partnerships and intervention studies, CBPR developed interventions are often unfunded or underfunded due to the complexities in which they are administered and within the prevailing political, social, and environmental interactions in which they occur [34]. Several partnerships and studies included in this review, discussed the challenges of not only sustaining the partnership, but also the funding over time to continue and to sustain the cessation intervention [13, 24, 25, 31, 32].

Besides strengths and challenges, this review also highlights the need for additional research. For example, several studies highlighted contributors to success in their partnership, such as “champions” and leaders at multiple levels within the community and engaged organizations who continue to facilitate the work and keep the partnerships mobilized [13, 1618, 24, 25]. Shared decision-making, communication processes, and mutual interest in the intervention were also frequently mentioned [13, 24,25, 31, 32]. These variables and others have been recently described in the literature as CBPR partnership readiness indicators [45,46]. While the concept of CBPR partnership readiness and related tools are emerging, additional research is needed to better understand how and why some partnerships are effective and others are not, as well as an improved understanding of levels of readiness and how to leverage partnership readiness (i.e., from partnership initiation to social action and policy change) for CBPR partners and their interventions.

Of the 11 studies included in this review, the two scoring highest in community involvement and research quality, demonstrated promise for effective cessation outcomes utilizing this approach [1013, 1619]. However, both of these studies were conducted with limited number of participants (i.e., 103–111 participants) and were pilot studies for larger randomized trials. The ability to sustain the partnerships, sustain the effects of the interventions, and promote policy and social action, are important aspects of CBPR to be achieved, yet little evidence exists on how to accomplish this. Further, is it possible to scale up a CBPR developed cessation intervention shown to be effective in one community to other heterogeneous communities for a randomized controlled trial? If the intervention is replicated in other communities, what additional CBPR processes need to be undertaken with the new communities to facilitate the buy-in, ownership, and adoption of the intervention? Further research will be needed to understand and guide best practices for these processes.

Finally, it is difficult to truly assess the “CBPR effect” of cessation interventions. Cessation intervention studies conducted with marginalized communities, regardless of CBPR or traditional approach, often vary in content, delivery, duration, and study design, making comparisons of outcomes a challenge [47]. As Buchanan and colleagues noted [3], to adequately test the CBPR effect, the ideal research design would be a cluster randomized trial that compared communities randomized to the CBPR process to a comparison condition of a traditional researcher-initiated investigation. This type of investigation, however, would be extremely complex and likely not practical [3].

There are several potential limitations of this review. The data compiled for this review, including quality scores, were derived from available published literature only. CBPR processes may not have been described in detail due to restrictions in publications (i.e., page limits). Further, the search strategy identified only articles published in peer-reviewed journals, and other dissemination materials from authors may have been excluded.

Conclusions

Although the quality of community involvement and research rigor varies, a well designed CBPR approach is showing promise in working with marginalized and “hard to reach communities” to promote cessation outcomes. A CBPR approach provides strengths in overcoming challenges in translating evidence into real-world settings, contextualizing the intervention, and sustaining long-term behavior change. Challenges, such as time requirements, complexities of the partnership and processes, IRB procedures, maintaining research rigor, and scaling up CBPR efforts to adequately test effects of interventions exist. This review provides a baseline of evaluation for current efforts of CBPR-developed smoking cessation interventions and recommendations to guide future intervention development and evaluation efforts.

Acknowledgments

Funding Support:

"This publication was supported by the South Carolina Clinical & Translational Research (SCTR) Institute, with an academic home at the Medical University of South Carolina, NIH/NCRR Grant number UL1 RR029882 and the National Institute of Heart Lung & Blood Institute, 5 R01HL090951-03. The contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH or NCCR.

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.

*

The authors have no financial disclosures and/or conflicts of interest to disclose.

Contributor Information

Jeannette O. Andrews, College of Nursing, Director, SCTR Community Engagement Core and Center for Community Health, Partnerships, Medical University of South Carolina, 99 Jonathan Lucas Street, MSC 160, Charleston, SC 29425-1600, andrewj@musc.edu, 843-792-1188.

Susan D. Newman, Center for Community Health Partnerships, College of Nursing, Medical University of South Carolina, Charleston, SC 29425 – 1600, newmansu@musc.edu, 843-792-9255.

Janie Heath, E. Louise Grant Endowed Chair, College of Nursing, Georgia Health Sciences University, 987 St. Sebastian Way, Augusta, Georgia 30912, jaheath@georgiahealth.edu, 706-721-0422.

Lovoria B. Williams, College of Nursing, Georgia Health Sciences University, 987 St. Sebastian Way EC-4511, Augusta, GA 30912, LWilliams@georgiahealth.edu, 706 721-4781.

Martha S. Tingen, Child Health Discovery Institute, Georgia Prevention Institute, Medical College of Georgia, Georgia Health Sciences University, Augusta, GA. 30912, mtingen@georgiahealth.edu, 706-721-0471.

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