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Community-based participatory research (CBPR) is an action research approach that emphasizes collaborative partnerships between community members, community organizations, health care providers, and researchers to generate knowledge and solve local problems. Although relatively new to the field of family social science, family and health researchers have been using CBPR for over a decade. This paper will introduce CBPR methods, illustrate the usefulness of CBPR methods in families and health research, describe two CBPR projects related to diabetes, and conclude with lessons learned and strengths and weaknesses of CBPR.
Community-based participatory research (CBPR) is an action research approach that emphasizes collaborative partnerships between community members, community organizations, health care providers, and researchers to generate knowledge and solve local problems (Doherty & Mendenhall, 2006; Israel, Eng, Schulz, & Parker, 2005; Minkler & Wallerstein, 2003). Hierarchical differences that typically arise between providers and patients are flattened through this partnership and all participants work together to co-create knowledge and effect change throughout all aspects of the research process (Mendennhall & Doherty, 2005; Lewin, 1946). Each partner contributes unique strengths and knowledge to improve the health and well-being of community members (Israel et al.; Minkler & Wallerstein).
CBPR has gained increased credibility in healthcare (e.g., medicine, nursing) and public health since the early 1990s because of its potential to inform understanding of individuals’ health-related experiences and inform the creation of workable and appropriate services (Heslop, Elsom, & Parker, 2000; Kovacs, 2000). CBPR has been used to address a wide variety of health issues in diverse communities, such as: hospice access and use by African Americans, mental health services for impoverished Hmong women, health audits, smoking cessation, primary care and diabetes management, dental and mouth-care practices, management of preoperative fasting, patient problem-solving skills, patient and practitioner satisfaction, patient-practitioner communication, and a number of other significant healthcare issues (de Amorim & Cavalcante, 1992; Hampshire, Blair, Crown, Avery, & Williams, 1999; Lindsey & McGuinness, 1998; McGarvey, 1993; McKibbin & Castle, 1996; Reese, Ahern, Nair, Faire, Warren, 1999; Yoshihama & Carr, 2002). Despite growth in other disciplines, CBPR is not widely used in family science or in families and health research. Thus, the purpose of this paper is to introduce CBPR methods, illustrate the usefulness of CBPR methods in families and health research, describe two CBPR projects related to diabetes, and conclude with lessons learned and both strengths and weaknesses of CBPR.
Several key tenets permeate CBPR projects (Israel, et al., 2005; Mendenhall & Doherty, 2003, 2005; Minkler & Wallerstein, 2003). First, CBPR acknowledges the community as a unit of identity in which all partners have membership. Second, CBPR emphasizes democratic partnerships between all project members as collaborators through every stage of knowledge- and intervention-development. Third, CBPR requires a deep investment in change that carries with it an element of challenging the status quo, improving the lives of members in a community and attending to social inequalities. Fourth, CBPR builds on strengths and resources within the community in order to address local concerns and solve relevant problems. Fifth, CBPR uses a cyclical process in which a problem is identified, solutions are developed within the context of the community’s existing resources, interventions are implemented, outcomes are evaluated, and interventions are modified in accord with new information as necessary. Sixth, CBPR promotes project partners’ humility and flexibility to accommodate changes as necessary across any part of a project and fosters co-learning and capacity building. Seventh, CBPR involves a long-term process and commitment to sustainability. (For a further review of CBPR see Minkler & Wallerstein and Mendenhall & Doherty, 2005.)
Due to the spreading interest in CBPR, authors have written about CBPR research conceptually and identified differing levels of involvement in which community members’ can participate. Arcury, Austin, Quandt, & Saavedra (1999) identified a broad range of what is considered CBPR, in that different members of a given community may take on varied roles in CBPR activities. “The range is characterized as active to passive, contractual to collegiate, and tokenism to degrees of citizen power” (p.564). They also emphasized that citizen power is the most effective type of active participation by community members, but is least likely achieved. Thinking of CBPR on a continuum of involvement by all stakeholders can produce beneficial outcomes. Our research corroborates the opinion that having community members involved at the highest level of collaboration, or utilizing “citizen power,” is the most effective and yields optimal outcomes, even though it requires more patience and diligence on the front end.
Although relatively new to family science research, community-based approaches can be linked to early family life education outreach efforts. There were several early roots connecting family life educators to community-based approaches. For instance, collaboration between church and state in the early 1800’s ensured that children were raised according to biblical standards. Similarly, child and mother community study groups (a type of support group) were created in the early 1900’s which became the Parent Teacher Association (PTA). Also, the growth of community-based parenting education programs in the 1920’s evolved into the National Extension Parent Education Model in the late 1990’s (Duncan & Goddard, 2005; Lewis-Rowley, Brasher, Moss, Duncan, & Stiles, 1993). More recently, CBPR has been used in family and health research by several family researchers (Author, 2008, in press; Garwick & Auger, 2003; Piercy & Thomas, 1998). In alignment with family systems thinking, which emphasizes the importance of relationships embedded in and across all aspects of family life (rather than focusing on the individual or community in exclusion of the family), CBPR methods have the potential to effect change on many system levels related to research, prevention, intervention, and education in the field of family science.
CBPR in families and health research is becoming more common due to its usefulness in activating individuals and families around the management of chronic conditions. Many chronic conditions have been resistant to traditional models of research inquiry due to the fact that traditional health care research typically aims to deliver health care “to” patients–rather than working “with” individuals and family members to increase ownership of the problem. CBPR is especially useful with families with members with chronic health conditions because family members, especially parents, typically struggle with how to help their family member without being overbearing or too protective (Berge & Holm, 2007; Berge & Patterson, 2004). CBPR allows family members to work together to find solutions in collaboration with professionals and community entities, which often get overlooked in traditional investigator driven research. Due to the highly collaborative nature of the method, the more people involved equates to more potential solutions and support for the implementation of the solutions. CBPR approaches have been found to be effective with chronic conditions in which provider and patient frustration is high due to poor disease management, such as diabetes, asthma, chronic pain, and depression (Davis, Clay, Smyth, Gittelsohn, Arviso, Flint-Wagner, et al., 2003; Garwick & Riesgraf, 2007; Mendenhall & Doherty, 2007; Mendenhall & Doherty, in press; Mendenhall, Doherty, Baird, & Berge, 2008).
We present two CBPR projects here that were guided by the Citizen Health Care model (Doherty & Mendenhall, 2006; Mendenhall et al., 2008). Our projects used the guiding principles and core strategies of the Citizen Health Care model because it is a CBPR approach applied specifically to the health care setting. As described elsewhere, the model includes six guiding principles (see Table 1) and seven core strategies (see Table 2) for implementing citizen action initiatives. It stresses the importance of civic engagement to strengthen family life, emphasizes the need to transcend traditional provider-consumer models of health care and professional service delivery, and offers a vision of families and professionals creating public initiatives together.
The Citizen Health Care Model is based on CBPR principles and tenets of the biopsychosocial systems model. First advanced by Engel (1977) and later extended by McDaniel, Hepworth, and Doherty (1992), the biopsychosocial systems model integrates multiple systems in the medical, behavioral health, and public health arenas, along with interactions among individuals, families, and health care providers. The model highlights the importance of collaborative work between professionals trained in a variety of disciplines, and utilizes treatments that attend to the complex, holistic nature of individuals’ and families’ experiences.
As outlined in Table 1, Citizen Health Care begins with the notion that all personal health problems can also be seen as public problems. For example, ethnic disparities in diabetes can be viewed in terms of its implications for an ethnic community’s sense of dignity and social pride. Similarly, depression can be viewed in terms of its consequences for families and the surrounding community. In addition, Citizen Health Care moves interdisciplinary collaboration from treating one individual at a time to collaborating with families and communities to effect change on a larger scale. The model is a systematic way to access a resource that is largely untapped in our contemporary health care system(s): the knowledge, lived-experience, wisdom, and energy of individuals and their families who face challenging health care issues in their everyday lives. The notion of “citizen” refers to individual and their families becoming activated along with their neighbors and others who face similar health challenges in order to make a difference for a community. Ordinary citizens become assets in heath care as they work as co-producers of health for themselves and their communities.
Table 2 outlines the main strategies for implementing the Citizen Health Care CBPR approach and “first steps” suggestions for initiating a project and community partnerships. These strategies and first steps have worked successfully for our research team as we have engaged a variety of communities in Citizen Health Care, tackling several important health care problems. The “ANGELS” project below will specifically highlight the “first steps” of a CBPR project.
One important element that is pervasive throughout the CBPR process is the aspect of “research”. Establishing statistical significance of CBPR projects is essential, otherwise the projects potentially could be misinterpreted to be program development projects only. Thus, a main focus of each project was to establish research elements from the beginning. The CBPR projects described below collected both qualitative and quantitative data that were agreed upon collaboratively by community members and researchers. Early on in the process the groups identified important research questions to investigate, including both community members’ and researchers’ agendas. As data were analyzed, findings were regularly presented back to the group who gave feedback regarding the accuracy, usefulness, and implications of the findings. The immediate relevancy of these data were ascertained in this process by the group, and data were acted upon (or not) according to this collaborative, self-sensitive feedback process.
Disseminating the research is another important aspect of CBPR. This allows for important findings to be distributed to both academic researchers and the families or community involved in the research. Results communicate success of the project, the changes brought about by the project, and the efforts of the researchers, families, and the community to sustain the project. In the following projects, researchers and community members have done several presentations together. Likewise, community members and researchers have done presentations and/or publications on their own. Each time a presentation or publication is submitted, a conversation ensues regarding who should be involved and in what capacity.
Similar to any new intervention study, CBPR projects begin as pilot studies that are honed and developed into randomized control trials. This is an important transition step, which brings credibility to the CBPR project. All of the projects mentioned below are in one of three stages: development (ANGELS), gathering pilot data (FEDS), or transitioning to an RCT (FEDS is now acquiring funding for an RCT). The “FEDS” project below will emphasize the “research process” of CBPR.
To improve the well-being of families who have adolescents living with diabetes.
Type 1 diabetes is the third most common chronic illness in youth (American Diabetes Association, 2005). Type 2 diabetes, once thought to occur almost exclusively in adults, is increasingly observed in childhood and adolescence (American Diabetes Association). Elevated diabetes among adolescence is a significant health concern because poor diabetes management in terms of glycemic control during adolescence is strongly associated with the onset and progression of a variety of short- and long-term diabetes-related complications in adulthood (Couper, Fotheringham, Taylor, & Sawyer, 1999; Hampson, Skinner, Hart, Storey, Gage, Foxcroft, et al., 2001).
Providers in the Pediatric Department of a large academic hospital had been frustrated for a long time with diabetes self-management with their adolescent patients. While some teens adhered to prescribed regimens of physical activity, diet, blood sugar monitoring, and insulin administration, a large proportion of individuals were managing their disease poorly. Conventional approaches to improving diabetes management such as teaching community classes about diabetes and self-care, and diabetes-related fairs and public forums were not effective for enhancing diabetes management. Similarly, warnings during standard care visits about a variety of long-term consequences associated with poor metabolic control were reported to be ineffective. Adolescents continued to evidence unhealthy physiological indicators of diabetes control, such as elevated hemoglobin A1c and body mass index, and they demonstrated little apparent motivation to change. Parents complained about being “nags” to teenagers who wanted to be left alone. Adolescents complained about adults (parents, providers) who would not “get off their backs” or allow them to have the same freedom and spontaneity as their peers. Providers felt triangulated into family conflicts, oftentimes while in the exam room, without any clear idea about what to do other than go over the same old information and cautionary warnings.
Initial conversations between the director of Pediatrics and University researchers ensued to identify new ideas for this old and increasing problem. The researcher suggested that a community-based participatory research approach be applied to this problem because it would move efforts beyond the conventional top-down services these adolescents and their families were resisting. The director had strong buy-in because he had seen numerous traditional attempts fail, but was optimistic that there was still an unknown solution yet to be found (action strategy #1; see Table 2). Not being familiar with interventions involving active individual and family participation in partnership with providers, but maintaining an investment to address the problem with an openness to try new solutions, the director mobilized other providers to meet (action strategy #2; see Table 2), learn about CBPR, and decide whether and how to proceed (action strategy #3; see Table 2).
Early meetings between researchers and providers addressed how to engage patients as collaborators in the design of supplemental services to standard care (action strategy #4; see Table 2). This would tap a variety of resources previously untapped, including individuals’ and families’ lived experience and wisdom of living with diabetes on a day-to-day basis. The Citizen Health Care Model was introduced as a guiding framework. The model views providers as citizens with specific knowledge and skills who work actively with other citizens who also possess important knowledge and skills. The model also argues that citizen partners must recognize and value the contributions that each member brings to the common mission, and that members must consciously and explicitly avoid conventional provider-consumer dynamics or hegemonic advantage to “experts”. Likewise, families are viewed as active producers and co-creators of action and change and do not function in a conventional consumer or patient role.
Six families, through their providers, were then invited to meet with providers and researchers to discuss ideas regarding the building of a citizen initiative that would benefit families whose adolescents were unsuccessfully managing their diabetes (action strategy #5; see Table 2). Adolescents and parents were enthusiastic about creating something new through CBPR, with the larger vision of developing a model of care by and for its citizens with all participants functioning as stakeholders in the process. Adolescents, in particular, were very active in the process because they felt listened to and valued. The group collaboratively identified key areas of concern and developed solutions within the contexts of the hospital and surrounding community’s resources. As adolescents, parents, providers, and researchers met over the following 6 months as the action planning group, an exciting new program was named by the group and began to take root (action strategy #6; see Table 2).
Through the ANGELS (A Neighbor Giving Encouragement, Love, and Support), adolescents and their parents who have lived experience with diabetes (called “support partners”) were connected with other families (called “members”) who were struggling with the illness. These efforts begin at the time of diagnosis, which occurs almost universally in the context of emergency hospitalization. It is during this time that the initiative’s teens maintained that they wanted the ANGELS to connect with members, because the motivation to adopt healthy lifestyles is the highest at a time of crisis. Support partners and members met at the time of hospitalization in a variety of combinations (e.g., adolescents with adolescents, parents with parents, families with families), and then continued to meet off hospital grounds (or via telephone, e-mail, internet discussion boards) after initial hospitalization. Sometimes members simply needed a pep talk; other times ongoing support was offered for several months. Adolescents and parents in the ANGELS program worked democratically with providers and researchers throughout every stage of its development – from initial brainstorming regarding the program’s mission, naming process, training design, public-visibility efforts, implementation, and ongoing problem-solving and maintenance (action strategy #7; see Table 2).
The ANGELS project is still in the development phase and the action planning group has been meeting to determine outcomes for a pilot project (Mendenhall & Doherty, 2007). For instance, they have identified outcomes such as: changes in diabetes control (A1c) and family functioning between groups receiving support through the ANGELS program in addition to standard care versus those receiving standard care exclusively (action strategy #7; see Table 2). Antidotal accounts suggest that the program’s usefulness will be further validated as these evaluative efforts are advanced.
Intentionally relying on existing community resources, the ANGELS program has maintained its democratic character and ensured its long-term viability as a resource within its community. Initial efforts are now in process regarding the training of a new generation of support partners – many of whom were members at one time that were connected with this program during their own crisis and early struggles with diabetes. Support partners’ sense of personal ownership in the ANGELS continues to be reflected in this progression as they assume responsibility for components of this training and long-term vision.
To improve the health of American Indian (AI) families and their family members who live with diabetes.
Diabetes is one of the most widespread chronic diseases in this country, with current prevalence estimates exceeding 6% of the general population (American Diabetes Association, 2005) The AI population is the hardest hit, with prevalence rates as high as 50% among certain tribes (Naylor, Schraer, Mayer, Lanier, Treat, & Murphy, 2003). Secondary prevention is also a critical concern, as AIs experience higher rates of diabetes-related complications – comorbid heart disease, reduced or lost vision, amputations, and kidney disease – compared to Caucasian and other ethnic groups (Parker, Haldane, Keltner, Strickland, & Tom-Orme, 2002).
AI community leaders and tribal elders in the Minneapolis / St. Paul area were worried about the ever-increasing prevalence of diabetes and its impact on families in the AI community. Intergenerational transmission of diabetes is common within AI tribes and many family members within the same generation frequently are living with diabetes. The pervasiveness of diabetes has been made even more alarming by the sense of defeat that many AI families communicate—that diabetes is expected and not preventable. Providers working with members of the AI community shared these concerns and were frustrated with the failure of conventional care to address these issues. They desired to address this “family problem” as a community and to find ways for families to feel empowered over the illness, rather than disempowered.
University of Minnesota (UMN) researchers, already situated within a health care clinic, and leaders in the St. Paul Department of Indian Work, already patients at the same clinic, had several informal conversations about the diabetes problem in AI families and the wider AI community. As they talked about the concerns regarding the sense of defeat, the researchers and community members decided to approach this challenge with a community-based participatory research paradigm, using Citizen Health Care as a guide. AI families in the community who were patients at the clinic were invited to participate in the action planning group. This was done by providers in the clinic nominating families who were managing diabetes well (though not perfectly). During the first six months of meeting together as an action planning group, considerable effort was spent in designing a partnership with providers that was very different than conventional top-down models of care. AI family community members succeeded in sensitizing clinical researchers regarding the process, pace, and importance of building trust within AI circles. As the team engaged in the ongoing meetings, discussions, and AI community events, this trust evolved. Researchers learned about AI culture, the diversity of cultures and tribes within this larger frame (e.g., Dakota, Ojibwe, Hocak), the importance of family, cultural belief systems, and manners. In turn, AI family community members gained more insight regarding how Western medicine is oriented and thereby gained insight into providers’ habitudes and perspectives in health care delivery.
After 6 months of the action planning group meeting, doing stakeholder interviews and creating an intervention, the Department of Indian Work’s (DIW) Family Education & Diabetes Series was implemented by community AI families, providers, and researchers as a supplement to standard care for families within the AI community who were touched by diabetes. Families (spouses, parents, children), the family member(s) with diabetes, and providers (physicians, nurses, dieticians, mental health personnel) came together every other week for an evening of fellowship, education, and support. Generally 6-7 providers, 4-5 tribal elders, and 12 families (approximately 35-40 community members) attended. Meetings began with all participants checking and recording each other’s blood sugars, weight, body mass index, and conducting foot checks. Families cooked meals together that were consistent with AI culture and traditions, and a great deal of discussion was put forth regarding the meal’s ingredients, portion sizes, and relevance to diabetes. Family meals were emphasized during this aspect of the project in order to address the common problems of: (a) eating individually or (b) the female head of household doing all the meal planning and cooking. Planning the menu and meal preparation were discussed as a “we” responsibility in order to help promote diabetes friendly meals and family connection. Educational sequences followed and took place in talking circles and across a variety of lively activities (e.g., traditional and modern music, chair dancing and aerobics, impromptu theater and role-plays). Instructional topics were similarly diverse, e.g., basic diabetes education, obesity, foot care, stress management, exercise, family relationships, retinopathy, dental care, and resources for medical services and supplies. FEDS evenings concluded with time for informal sharing and support. These bi-weekly series were scheduled to last for three hours, but most families arrived early and stayed late.
At the beginning of the CBPR process (approximately 3 months into the process), the action planning group discussed the research elements of the project. It was determined early on that hemoglobin A1c levels, weight, blood pressure, knowledge of diabetes, and psychosocial stress would be measured. These outcomes were identified by determining which issues each member of the action planning group was most worried about for AI families who were dealing with diabetes. As the issues were discussed a list was created and variables that could potentially measure these concerns were identified (e.g., concern = heart attack as complication of diabetes, variable to measure = blood pressure, weight, & A1c; concern = family stress, variable to measure = psychosocial stress). During this CBPR process one stakeholder’s perspective was not given advantage over another’s thus, outcome variables were not included unless all parties agreed. All assessment measures being utilized in the study were also examined and approved by the action planning group comprised of AI families, providers, and researchers. One example of the importance of using this CBPR process was made overt when the psychosocial assessment instrument was being discussed. The AI family community members identified that there was very sensitive material regarding sexual intimacy on the instrument. The providers and researchers were told that this would not be respectful to AI culture and that families may become suspicious of the research, or may not even participate, if the entire instrument was used. The action planning group decided to remove the subscale that involved sensitive material and use the rest of the instrument. This decision was beneficial because it did not alter the research question(s) being answered but did increase the likelihood of participation.
Data collection was also collaboratively done. The action planning group decided that AI family community members would be more trusting of data collection if other AI families were involved in the collection process. The action planning group also wanted to promote diabetes self-management skills, and by having AI family members collect each other’s data, they would also be learning how to improve their diabetes self-management skills. Thus, AI family members collected data that was appropriate to collect (weight & BMI, foot checks, exercise logs, blood sugars), and the providers and researchers collected data that was specialist-specific (paper assessments, A1c levels, and blood pressure). AI family community members, providers, and researchers were all present at the FEDS meetings in order to promote the idea of a partnership and co-creation of health.
As analyses were run by the researchers, the action planning group discussed the results and next steps. Many positive changes were seen related to weight, A1c, and psychosocial stress. One area that was not showing improvement, and in some cases was getting worse, was diabetes knowledge. The action planning group decided to investigate potential problems with this variable. The instrument itself was re-visited, how the information was being taught was looked at, and how the instrument was administered to the participants was examined. It was decided that how the information was being taught was not translatable into laypersons language. In the next series an AI elder taught the session about diabetes 101 and the diabetes knowledge score for participants went up or stayed consistent (rather than decreasing or being inconsistent).
As the project evolved, the action planning group discussed presentations and publications. It was decided by the action planning group that each time a presentation or publication was submitted, a conversation would ensue regarding who should be involved and in what capacity. Over 15 presentations have been done to-date, in which about half have been with family members of the AI community, providers, and researchers, while the other half have been done by researchers themselves or by AI family community members. Several publications have also resulted from this work. The action planning group decided that communicating the results of the project to a broad audience was important. Thus, some of the publications have been in academic peer reviewed journals, and others have been in newsletters, newspapers, or reports. Authorship was determined beforehand and followed a pre-set pattern. For example, the first author must be directly connected to the venue in which the article will be published (e.g., academic journal = researcher, medical newsletter = provider, newspaper, or community report = AI community family member). Grants have also been written collaboratively. The action planning group determined that the researchers would write the initial drafts of the grant; the AI community family members and providers then gave feedback on the draft, and final approval of the grant was given by the entire action planning group.
Pilot data (n = 40) has shown significant improvements in participants’ (individual with diabetes and family members) blood pressure and weight. Of note, participants with diabetes hemoglobin A1c levels have also significantly improved (Mendenhall, Berge, & Harper, under review). The results of this pilot data are now being used to obtain funding for a randomized control trial to test this intervention against a control group.
The above projects represent two of 13 CBPR projects that our research team has conducted over the past nine years (half specifically related to families and health issues). Many lessons have been learned from these projects (see Table 3). Also, we recognize there are strengths and weaknesses to every research approach; accordingly, below are a number of strengths and weaknesses inherent to CBPR. The strengths relate to the utility of CBPR in improving family and health research (broadly defined) and benefiting the lives of a community’s members. The limitations serve as cautions to those engaging in this type of inquiry, as well as challenges for those wishing to advance CBPR.
CBPR is carried out in the very context(s) that researchers seek to benefit (Coghlan & Casey, 2001; Piercy & Thomas, 1998). Families in the community define their concerns, develop and implement solutions to local-level problems with local-level resources, and take an active role in the research process. Instead of ever having to move research into the “real world” through practice and application, CBPR is conducted in the real world and utilizes investigation and action as inseparable facets of its overall course—what is produced is immediately relevant (Hambridge, 2000; McKibbin & Castle, 1996; Meyer, 2000).
CBPR taps resources that already exist in families and communities, but which have been underutilized or entirely untapped. These resources can be personal (e.g., leadership skills, lived-experience, and wisdom) or tangible (e.g., money, services), but they are not created through external funding. While external funding is often used to support the project, members gain an increased sense of ownership by identifying and using participant resources in solving the problem (Casswell, 2000; Hagey, 1997; Minkler, 2000).
CBPR’s forward-vision challenges the status quo, and its participants engage actively in the process. The democratic processes between professionals, families and community members facilitate a flat hierarchy so that all work together to generate knowledge and affect change. Participants and family members who once felt disempowered become empowered as stakeholders in the CBPR process. As all develop a sense of co-ownership in identifying problems and solving them, CBPR participants shift from an identity of passive recipients of inadequate services to active members of a team passionately invested in change (Hambridge, 2000; Piercy & Thomas, 1998).
CBPR is marked by a series of trials and errors through the iterative processes of identifying problems and generating solutions to improve the lives of a community (Hagey, 1997; Lindsey & McGuinness, 1998). It is common for participants in CBPR initiatives to see early efforts as completely or partially unsuccessful. Often researchers must return to the drawing board in order to accomplish the initiative’s shared goals. Unlike conventional research projects in which a timeline for participant recruitment, data collection, data analysis, and reporting of results can be tentatively outlined, CBPR can be entirely unpredictable. This can be frustrating to members in the CBPR process, and professional entities who are evaluating a researcher’s productivity are not as likely to be sensitive to this.
In addition, external funding at the outset can be a trap because of timelines and deliverables. Until recently, major grant funders (such as the National Institutes of Health) have not been eager to fund CBPR. Because CBPR is an iterative process with the end project usually looking very different from the beginning conceptualization, funders have been reluctant to fund such projects. However, our experience indicates that it is possible to describe specific outcomes that a CBPR project will address and measure with specific deliverables, while still maintaining the importance of the iterative CBPR process as a main component of the project. We have successfully obtained over eight grants to fund CBPR projects. We have also noticed, delightedly, an increase in program announcements from NIH and other funders calling for CBPR projects.
Still problematic is how CBPR is perceived by universities’ institutional review boards (IRBs) and how these regulatory bodies can be convinced that this type of research is acceptable in terms of participant safety and issues of confidentiality. Due to the ambiguity of what is ultimately going to result from CBPR efforts, it is difficult to meet standard notions of what informed consent requires. Also, the public nature of CBPR initiatives makes it challenging to maintain participants’ confidentiality. It is difficult to maintain anonymity in research write-ups, particularly since the participants are also the co-researchers. There are no easy answers to these questions as yet.
CBPR is here to stay, as evidenced by its increasing visibility in families and health research and healthcare circles. As our efforts to improve community problems and practice charge forward, so has our need to employ research strategies that permit analyses of information and the incorporation of change processes in real-time (Greenwood, 1994; Hampshire et al., 1999; Meyer, 2000). As these efforts proceed and we continue to work together to improve communities through any variety of actions, the following points are important to consider:
CBPR efforts must recognize the valuable knowledge and wisdom that multiple participants bring to the table. Many CBPR projects, however, do not involve professionals from a variety of disciplines. As professionals from a diversity of fields (e.g., medicine, nursing, social work, family science, marriage and family therapy, anthropology) employ CBPR, efforts to collaborate across disciplines will not only be practical, but also sensible, because they combine a discipline’s strengths with those of others around the table (Mendenhall & Doherty, 2003; Small, 1995).
CBPR has not yet received a great deal of attention in graduate research courses and young professionals’ exposure to this type of work is limited as a consequence (McNicoll, 1999; Small, 1995). Increasing CBPR’s visibility in graduate education will better prepare our next generation of researchers and practitioners to engage in investigatory efforts that are designed to immediately benefit the communities where they live. A challenge to this call rests in the likelihood that many of the professionals who are teaching graduate research are not, themselves, familiar with this approach. Current educators, therefore, maintain the responsibility to learn about CBPR in order to facilitate students’ learning.
We must also continue to increase CBPR’s visibility on a larger scale across professional arenas. This may take the form of publication in mainstream refereed journals, or increased attention in national and international forums through public presentations, posters, or discussion groups. All such efforts that facilitate widespread familiarity and exposure to CBPR will serve to augment and stabilize its position as an accepted research practice in family science and healthcare science. Its potential will only be realized when CBPR becomes an increasingly common way of working with families and communities. See Table 4 for several exemplar CBPR projects done in a variety of professional fields.
As mentioned earlier, major grant funders have been reluctant to fund CBPR projects. Recent changes, such as program announcements from NIH and other funders calling for CBPR projects, indicate promise for such research. CBPR researchers should continue to present and publish their findings in order to bring more visibility to this methodology. As funders continue to see the positive outcomes from CBPR projects they will continue to offer grant funding for these projects. Likewise, as more researchers are funded for CBPR projects the amount of grant money available will increase.