Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2018 Dec 1.
Published in final edited form as: Psychiatr Serv. 2017 Nov 1;68(12):1315–1320. doi: 10.1176/appi.ps.201700170

Comparative Effectiveness of Community Coalition Building versus Program Technical Assistance for Depression Services Quality Improvement: Do Both Health and Community-based Sector Clients Benefit?

Cathy D Sherbourne 1, Wayne Aoki 2, Thomas Belin 3, Elizabeth Bromley 4,5, Bowen Chung 6,7, Elizabeth Dixon 8, Megan D Johnson 9, Felica Jones 10, Paul Koegel 11, Dmitry Khodyakov 12, Craig Landry 13, Elizabeth Lizaola 14, Norma Mtume 15, Victoria Khanh Ngo 16, Michael Ong 17,18, Judith Perlman 19, Esmeralda Pulido 20, Vivian Sauer 21, Lingqi Tang 22, Yolanda Whittington 23, Ed Vidaurri 24, Pluscedia Williams 25, Aziza Lucas Wright 26, Lily Zhang 27, Jeanne Miranda 28, Loretta Jones 29, Kenneth Wells 30,31
PMCID: PMC5872839  NIHMSID: NIHMS941288  PMID: 29089009

Abstract

Objective

To compare effectiveness of Community Engagement and Planning (CEP) and Resources for Services (RS) for depression collaborative care, among healthcare and community sector clients.

Methods

In under-resourced communities, within 93 programs randomized to CEP or RS, 1,246 depressed clients enrolled; 1,018 completed baseline, 6, 12, or 36-month surveys. Regressions estimated intervention and intervention-by-sector interaction effects on depression and mental health-related quality of life, community-prioritized outcomes and services use.

Results

For outcomes, there were few significant interactions and stratified findings suggest CEP client benefits in both sectors. For services use, significant 36-month interactions suggest greater increase under CEP in primary-care, self-help visits and appropriate treatment for community clients; and in community-based services for healthcare clients.

Conclusion

Findings suggest CEP relative to RS benefited clients across sectors and shifted long-term utilization across sectors. Implementation of depression collaborative care may expand its reach by inclusion of community as well as healthcare sector clients.


Depressive disorders are associated with increased morbidity and mortality (1), with racial and ethnic disparities in access, quality and outcomes of depression services (2). Studies document effectiveness of collaborative care for depression in primary care, which may reduce racial/ethnic outcome disparities (3). Such programs are often unavailable in under-resourced communities, where individuals may seek help outside of healthcare (4). To address such disparities, Community Partners in Care (CPIC) compared two approaches to implement an expanded model of depression collaborative care across healthcare (primary care, public health, mental health, substance abuse programs) and community sectors (homeless and social services, faith-based, hair salons, park senior centers, exercise clubs) (5).

One model, Resources for Services (RS), used expert technical assistance to provide trainings and resources to individual programs for improving depression services based on collaborative care models that also supported non-licensed staff (4, 6, 7). The other model, Community Engagement and Planning (CEP), supported coalitions across healthcare and community sectors to collaborate in expanded collaborative care for depression. For largely ethnic minority depressed clients from all sectors, those in CEP compared to RS improved in mental health-related quality of life (MHRQL) (6 and 12 months), physical exercise (6 months) and physical health-related quality of life (PHRQL) (36 months); had reduced probability of multiple homelessness risk factors (6 months), behavioral health hospitalization (6 and 12 months) and fewer hospitalization nights (36 months); fewer specialty medication visits and more faith-based and park/senior center depression services (6 months); and greater probability of any community sector depression services at 36 months. There were no significant intervention effects on depressive symptoms, but also no usual-care group.

Studies of collaborative care focus on healthcare patients, rather than similar depressed individuals in social-community settings who may not use health services. We have not previously reported intervention effects separately for clients from these two different sectors, and overall intervention effects could be largely limited to healthcare clients with greater treatment access; or effects could differ with healthcare clients having health gains and community clients having social gains. Evidence of benefits of the coalition model across sectors could suggest that a community-wide approach drawing clients from diverse sectors may be beneficial for addressing disparities. There are few available data on coalition compared to technical assistance approaches to collaborative care for largely minority communities (8).

This study examines intervention-by-sector interaction effects on outcomes and long-term services utilization, and explores stratified findings on outcomes to confirm whether there is evidence for CEP benefits within each sector. We anticipated that some initial benefits (6,12 months) of CEP compared to RS in the whole sample would apply to each sector. We expected that by 3 years, due to greater emphasis on collaboration, CEP compared to RS would lead to greater services use outside of the sector where clients were identified (e.g., healthcare use by community clients and community service use by healthcare clients). The study is hypothesis-generating on how coalitions relative to technical support may affect clients in different sectors.

METHODS

Data are from CPIC (5), a group-randomized trial using Community-Partnered Participatory Research to promote equal leadership of community and academic partners (9). South Los Angeles and Hollywood-Metro were selected as under-resourced communities. Institutional review boards of RAND and participating agencies approved procedures, with post-enrollment ClinicalTrials.gov registration (NCT01699789). Informed consent was obtained from clients.

CPIC’s interventions encouraged but did not require use of depression services QI toolkits(4, 6, 7) (http://www.communitypartnersincare.org/community-engagement/cep/).

RS provided free technical assistance to individual programs for these toolkits, using a “train-the-trainer” model offered to program representatives via 12 phone or on-line webinars over two months. Representatives were encouraged to share toolkits with staff. A physician offered one site visit per primary-care site on medication management and clinical assessment. Referrals were made for supervision in Cognitive Behavioral Therapy.

CEP supported participating programs in each community in developing a coalition for developing and implementing a training plan and monitoring depression services based on the same toolkits. Program liaisons met bi-monthly for 4 months, supported by intervention experts and $15K per coalition for innovations in toolkit adaptations, and monthly for a year for monitoring and developing innovations. Lists of participating clients were provided to CEP but not RS administrators for safekeeping in a locked file.

As described elsewhere (5), from November 2008 to August 2010, health and community-based programs serving adults or parents of child clients were identified. Within eligible and recruited agencies, eligible programs, (i.e., providing services to ≥15 clients/week, having ≥2 staff or ≥1 staff for small programs, identifying a liaison and not focused on psychotic disorders or home services) were enumerated, including programs serving four community-prioritized groups: homeless, seniors, African Americans, and substance abuse programs. From 60 agencies, 133 programs were paired into units based on community, sector, size and funding sources and randomized to each intervention. At follow-up visits to confirm eligibility, 95 programs from 50 agencies enrolled. Participating and nonparticipating programs had comparable neighborhood characteristics (5).

Staff blinded to intervention assignment screened clients for eligibility in 2-3 day periods per program. Eligible clients were age ≥18 years, spoke English or Spanish, provided contact information, and were depressed (8-item Patient Health Questionnaire, modified PHQ-8 ≥ 10) and not grossly cognitively impaired. Of 4,649 adults approached March, 2010 to November, 2010, 4,440 (96%) agreed to screening in 93 programs; 1,322 (30%) were eligible; 1,246 (94%) consented; 981 (79%) completed baseline telephone surveys (April 27, 2010-January 2, 2011). Participants not refusing follow-up were invited to complete 6 and 12-month surveys. Enrollees with any survey data who had not refused follow-up or were known to have died were invited for 36-month surveys (5, 10) (Ong, in press).

Covariates include age, community, education, race/ethnicity, 12-month major depressive or dysthymic disorder (11) and baseline measure of each outcome.

Pre-specified primary outcomes are poor MHRQL (MCS-12 ≤ 40(12)) and probable depression (PHQ-8 ≥10(13)). Outcomes prioritized by community stakeholders were mental wellness (at least “sometimes in the prior 4 weeks” feeling calm or peaceful, having energy, or being happy (5)), PHRQL (PCS-12) (12); homelessness risk, i.e., homeless or living in a shelter or having 2 or more risk factors (i.e., no place to stay for 2 or more nights, eviction from a primary residence, financial crisis or food insecurity in the past 6 months); and behavioral health hospitalization nights.

Secondary outcomes included outpatient visits in the prior 6 months to health agencies (e.g., primary care, emergency or urgent care, specialty medication and counseling visits, any healthcare visit) and community agencies (e.g., social services for depression, any community depression services including social service, faith-based, parks, telephone hotline, and other places for information, referral, counseling, or medication management for depression/mental health) (5). Depression services were defined by participant report of receiving assessment, treatment or referral services. We summed “depression” visits and mental health self-help/family support visits. Treatment indicators included: use of antidepressants (5, 6) and probable appropriate treatment(6), defined as not depressed (PHQ-8<10) or having ≥2 months of antidepressant use or ≥4 specialty or primary-care-depression visits.

We compared baseline characteristics by intervention status within sector for the 1,018 analytic sample, with item-level imputation for missing data (14) and wave-level imputation for missing surveys adjusting to the analytic sample; and weights to account for non-enrollment and attrition (see Appendix). Main analyses used Taylor series linearization with SUDAAN version 11.0.1 (http://www.rti.org/sudaan/), accounting for clustering, weighting, and multiple imputations.

We conducted intent-to-treat analyses with intervention status as the main independent variable, screening sector and intervention-by-sector interactions for estimating intervention effects within sector, categorized as “healthcare” (i.e., primary care/public health, mental health or substance abuse program) or “social-community” (i.e., homeless, social service, faith-based, park senior center, hair salon, exercise or other program). With attrition as a limitation (8), we present end-status as main analyses, permitting multiple imputation and response weights; and unweighted longitudinal trajectory sensitivity analyses (Appendix).

We used linear regression for continuous, logistic for binary, and Poisson for count variables, adjusted for baseline status of dependent variable and covariates. Results are presented from linear models as between-group differences, logistic as odds ratios (ORs), and Poisson as incidence rate ratios (IRRs), with 95%-confidence intervals; illustrated by standardized predictions from fitted regression models. As exploratory analyses, we do not adjust for multiple comparisons but discuss implications.

RESULTS

Of the analytic sample, 715 were from healthcare and 303 from social-community sectors. Baseline factors did not differ significantly by intervention status within sector, except in the social-community sector, where CEP clients were on average 6 years older than RS (p=.03). Most participants were African American or Latino and had family income below federal poverty (Appendix).

Intervention-by-sector interactions were not significant except CEP compared to RS was associated with greater reduction at 6 months in behavioral health hospitalization nights for community than healthcare clients (IRR=.3, CI=.1-1.0, p=.04). In stratified analyses, CEP compared to RS was associated with a lower likelihood (OR=.7, CI=.5-0.9, p=.015) of poor MHQL at 6 months for healthcare clients and at 12 months for social-community clients (OR=.6, CI=.3-1.0, p=.045). CEP compared to RS was associated among healthcare clients with a higher likelihood of mental wellness at 6 months (OR=1.9, CI=1.0-3.3, p=.039) and greater PHRQL at 36 months (between-group difference=1.6, CI=.2-3.0, p=.025); and among social-community clients with less homelessness risk at 6 months (OR=.4, CI=0.2-0.9, p=.018).

There are few significant interactions or within-sector intervention effects for outpatient use at 6 or 12 months (Table 1). Among healthcare clients there was reduced use of mental health specialty medication visits at 6 months (IRR=.4, CI=.2-.6, p<.001) and antidepressants at 12 months for CEP compared to RS clients. At 36 months, significant interactions showed greater increases under CEP compared to RS for community clients in primary-care visits, mental health self-help or family support-group days, use of antidepressants and antipsychotics, probable appropriate treatment, and a trend for any healthcare visits; yet greater increases for healthcare clients in social-service depression visits and any community-program depression visit (each p<.01). Longitudinal analyses confirmed these interactions as significant (see Appendix).

TABLE 1.

Client Secondary Outcomes by Intervention Status from Intervention-by-Sector Interaction Model*

Social-community Screening Sector Healthcare Screening Sector

RS Estimate CEP Estimate CEP vs RS RS Estimate CEP Estimate CEP vs RS Interaction

Mean 95%CI Mean 95%CI IRR 95%CI p Mean 95%CI Mean 95%CI IRR 95%CI p p
Health Services
No. of visits to a PCP
 6-mo follow-up 4.0 2.7-5.8 3.9 2.9-5.2 1.0   .6-1.6 .944 4.5 3.1-6.4 3.9 3.3-4.6   .9   .6-1.3 .484 .709
 12-mo follow-up 3.0 2.3-3.9 3.7 2.7-5.1 1.2   .8-1.9 .338 3.2 2.3-4.4 3.5 3.0-4.2 1.1   .8-1.6 .580 .671
 36-mo follow-up 2.4 2.0-2.9 4.5 3.1-6.4 1.9 1.3-2.8 .003 4.5 3.0-6.7 4.0 3.2-4.9   .9   .6-1.4 .578 .035

% % OR % % OR

Any visit in healthcare sector
 6-mo follow-up 86.6 80.5-91.1 84.5 75.5-90.8   .8   .4-1.8 .646 90.9 86.6-94.0 89.2 84.0-92.9   .8   .4-1.6 .533 .950
 12-mo follow-up 80.2 70.4-87.3 84.4 77.6-89.4 1.4   .7-2.7 .375 83.5 78.6-87.5 84.5 78.6-89.0 1.1   .7-1.8 .770 .592
 36-mo follow-up 75.3 67.4-81.9 85.8 76.0-92.0 2.0   .9-4.5 .082 87.7 79.5-93.0 83.9 73.1-91.1   .7   .3-1.6 .402 .025
Community Services
Any social services for depression
 6-mo follow-up 19.0 14.0-25.4 13.7 8.8-20.6   .7   .3-1.3 .203 17.0 12.4-22.9 19.0 14.5-24.5 1.2   .7-1.9 .578 .126
 12-mo follow-up 12.9   8.2-19.7 8.8 3.9-17.9   .6   .2-1.9 .376 9.5   5.8-14.9 12.7   9.2-17.2 1.4   .7-2.8 .315 .133
 36-mo follow-up 18.8 11.0-29.9 9.3 3.8-20.3   .4   .1-1.3 .122 10.5   7.0-15.5 21.0 13.3-31.2 2.3 1.1-4.8 .030 .034
Any community sector visit for depression
 6-mo follow-up 28.2 21.4-36.1 29.4 22.3-37.7 1.1   .6-1.8 .813 29.8 24.4-35.8 31.9 25.1-39.6 1.1   .7-1.7 .633 .892
 12-mo follow-up 20.8 15.3-27.5 21.8 14.1-31.8 1.1   .5-2.2 .859 20.4 16.1-25.5 24.1 19.5-29.3 1.2   .8-1.9 .285 .640
 36-mo follow-up 31.0 22.1-41.5 25.4 17.1-36.0   .8   .4-1.4 .337 27.3 21.9-33.4 39.8 32.2-47.9 1.8 1.2-2.8 .009 .036
Community and/or Healthcare service

No. of days attended self-help or family support groups for MH problem Mean Mean IRR Mean Mean IRR

 6-mo follow-up 2.6 1.1-6.2 4.3 2.0-9.0 1.6   .5-5.1 .395 6.4 3.5-11.2 4.4 2.8-6.9   .7   .4-1.3 .262 .180
 12-mo follow-up 2.6   .8-7.8 6.5 3.0-14.0 2.6   .7-10.0 .169 8.8 6.1-12.6 5.0 2.8-8.9   .6   .3-1.0 .060 .046
 36-mo follow-up 2.1 1.0-4.3 6.4 3.5-11.4 3.1 1.2-8.1 .024 7.9 5.1-12.1 5.3 2.8-9.7   .7   .3-1.6 .301 .033
No. of outpatient contacts for depression all sectors
 6-mo follow-up 17.2 9.4-30.9 21.2 14.5-30.8 1.2   .6-2.6 .541 24.9 17.8-34.7 22.2 16.7-29.4   .9   .5-1.5 .628 .350
 12-mo follow-up 9.8 5.6-16.9 17.0 10.5-27.5 1.7   .8-3.7 .147 21.9 17.0-28.2 17.2 12.2-24.3   .8   .5-1.1 .190 .047
 36-mo follow-up 10.7 6.9-16.5 17.2 10.9-26.9 1.6   .8-3.0 .144 25.8 19.7-33.6 21.3 13.5-33.2   .8   .6-1.2 .305 .054
Treatment

Use of any antidepressant % % OR % % OR

 6-mo follow-up 31.4 24.4-39.2 30.6 21.0-42.2 1.0   .5-2.0 .894 44.0 34.7-53.7 35.5 28.3-43.4   .6   .4-1.2 .131 .300
 12-mo follow-up 28.4 19.6-39.2 30.7 22.0-41.0 1.1   .5-2.5 .743 39.3 32.0-47.0 29.1 24.3-34.4   .6   .4-0.9 .016 .143
 36-mo follow-up 14.2 9.2-21.2 33.1 24.7-42.6 3.2 1.6-6.4 .002 34.5 27.4-42.3 24.4 15.8-35.3   .6   .3-1.2 .135 .011
Probable appropriate treatment
 6-mo follow-up 74.1 65.0-81.0 75.5 67.2-82.3 1.1   .6-2.1 .802 77.9 69.6-84.5 79.2 74.1-83.6 1.1   .7-1.8 .727 .991
 12-mo follow-up 70.6 57.1-81.3 73.6 63.0-82.0 1.2   .5-2.5 .693 76.6 71.7-80.9 72.8 64.8-79.6   .8   .5-1.2 .327 .427
 36-mo follow-up 60.5 43.9-75.2 76.9 65.7-85.4 2.2 1.1-4.5 .033 72.8 65.1-79.4 65.5 57.4-72.9   .7   .4-1.2 .169 .031

DISCUSSION

We found no consistent, significant intervention-by-sector interactions on outcomes, suggesting results for the combined sample largely apply across clients identified in healthcare and community sectors. In addition, stratified findings, confirmed by longitudinal sensitivity analyses, reinforce potential benefits of CEP relative to RS within each sector at some time point, in this largely ethnic minority sample. Thus, inclusion of community-sector depressed clients, unusual for a collaborative care study, may be a promising way to extend the reach of depression interventions otherwise largely limited to healthcare clients and sectors.

Findings on long-term outpatient use suggest that CEP’s network approach relative to RS’s technical support, 2 years after study intervention support ended, may over time have increased community clients’ use of healthcare depression services and healthcare clients’ engagement in community depression services. Whether this pattern reflects client learning from initial exposure or effects of persistent network ties, is an issue for future research, as is whether these shifts in utilization improve later outcomes. The level of significance, consistency across models, and affecting multiple utilization indicators, suggests despite multiple comparisons that effects may be real and merit potential replication in future studies.

Limitations include self-report measures, program-level randomization within two communities, multiple outcomes with few significant interactions and an exploratory approach.

CONCLUSION

This study may inform future studies of community health homes seeking to reduce disparities. Findings suggest that it is feasible and may expand the reach of collaborative care (15) to include in such efforts not only clients from traditional healthcare sectors but those with similar needs from social-community sectors.

Supplementary Material

supplement

Acknowledgments

This CPIC outcome study was supported by the Patient Centered Outcomes Research Institute (PCORI) contract # 1845 for the 3-year extension study, R01MD007721 from the National Institute on Minority Health and Health Disparities for subgroup analyses and the parent CPIC study by R01MH078853, P30MH082760 and P30MH068639 from the National Institute of Mental Health; the parent CPIC study was also funded by 64244 from the Robert Wood Johnson Foundation, CMCH-12-97088 from the California Community Foundation, G08LM011058 from the National Library of Medicine, and UL1TR000124 from the NIH/National Center for Advancing Translational Science UCLA CTSI. The RAND Corporation, UCLA Semel Institute and the Los Angeles County Departments of Mental Health, Public Health and Health services provided institutional support. We thank 95 participating healthcare and community-based agencies, the CPIC Council and members of the Association of Clinical and Translational Science Team Science Award for CPIC (2014) and Campus-Community Partnerships for Health 2015 Annual Award. We acknowledge posthumously the contributions to study design and implementation of two CPIC Council leaders (Rev. Ron Wright and Rev. Terrance Stone) who passed away during preparation of this manuscript. We thank Erika Orellana for support for manuscript preparation.

Footnotes

DECLARATION OF INTERESTS

The authors report no financial relationships with commercial interests.

Contributor Information

Cathy D. Sherbourne, RAND Corporation

Wayne Aoki, Los Angeles Christian Health Centers, Los Angeles, California.

Thomas Belin, UCLA Fielding School of Public Health- Biostatistics, Los Angeles, California.

Elizabeth Bromley, UCLA - Semel Institute Center for Health Services and Society, Los Angeles, California; West Los Angeles Veterans Administration Healthcare System - Desert Pacific MIRECC, Los Angeles, California.

Bowen Chung, Los Angeles County Department of Mental Health; UCLA-Semel Institute Center for Health Services and Society, Los Angeles, California.

Elizabeth Dixon, UCLA – School of Nursing, Los Angeles, California.

Megan D. Johnson, Kaiser Permanent Southern California Department of Psychiatry, Los Angeles, California

Felica Jones, Health African American Families II (HAAF), Los Angeles, California.

Paul Koegel, RAND Corporation – Health, Santa Monica, California.

Dmitry Khodyakov, RAND Corporation, Los Angeles, California.

Craig Landry, University of California Los Angeles David Geffen School of Medicine, Los Angeles, California.

Elizabeth Lizaola, UCLA Semel Institute- Center for Health Services and Society, Los Angeles, California.

Norma Mtume, Shields for Families, Los Angeles, California.

Victoria Khanh Ngo, RAND Corporation – Health, Santa Monica, California.

Michael Ong, UCLA Geffen School of Medicine – General Internal Medicine, Los Angeles, California; West Los Angeles Veterans Administration Healthcare System - Desert Pacific MIRECC, Los Angeles, California.

Judith Perlman, RAND Corporation – Rand Health, Los Angeles, California.

Esmeralda Pulido, LA Care, Los Angeles, California.

Vivian Sauer, Jewish Family Services of Los Angeles, Los Angeles, California.

Lingqi Tang, UCLA Semel Institute Center for Health Services and Society, Los Angeles, California.

Yolanda Whittington, LA County Department of Mental Health, Los Angeles, California.

Ed Vidaurri, LA County Department of Mental Health, Los Angeles, California.

Pluscedia Williams, Healthy African American Families (HAAF), Los Angeles, California.

Aziza Lucas Wright, RAND Corporation – Health, Santa Monica, CA.

Lily Zhang, UCLA Semel Institute Center for Health Services and Society, Los Angeles, California.

Jeanne Miranda, UCLA Semel Institute Center for Health Services and Society, Los Angeles, California.

Loretta Jones, Healthy African American Families II (HAAF), Los Angeles, California.

Kenneth Wells, RAND Corporation, Santa Monica, California; UCLA Geffen School of Medicine- Psychiatry and Behavioral Sciences, Los Angeles, California.

References

  • 1.Kessler R, Chiu W, Demler O, et al. Prevalence, severity, and comorbidity of 12-month DSM-IV disorders in the National Comorbidity Survey Replication. Archives of General Psychiatry. 2005;62:617–27. doi: 10.1001/archpsyc.62.6.617. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Miranda J, McGuire T, Williams D, et al. Mental health in the context of health disparities. American Journal of Psychiatry. 2008;165:1102–8. doi: 10.1176/appi.ajp.2008.08030333. [DOI] [PubMed] [Google Scholar]
  • 3.Gilbody S, Bower P, Fletcher J, et al. Collaborative care for depression: A cumulative meta-analysis and review of longer-term outcomes. Archives of Internal Medicine. 2006;166:2314. doi: 10.1001/archinte.166.21.2314. [DOI] [PubMed] [Google Scholar]
  • 4.Miranda J, Chung JY, Green BL, et al. Treating depression in predominantly low-income young minority women. Journal of the American Medical Association. 2003;290:57–65. doi: 10.1001/jama.290.1.57. [DOI] [PubMed] [Google Scholar]
  • 5.Wells KB, Jones L, Chung B, et al. Community-partnered cluster-randomized comparative effectiveness trial of community engagement and planning or resources for services to address depression disparities. Journal of General Internal Medicine. 2013;28:1268–78. doi: 10.1007/s11606-013-2484-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Wells KB, Sherbourne C, Schoenbaum M, et al. Impact of disseminating quality improvement programs for depression in managed primary care. Journal of the American Medical Association. 2000;283:212. doi: 10.1001/jama.283.2.212. [DOI] [PubMed] [Google Scholar]
  • 7.Unützer J, Katon W, Callahan CM, et al. Collaborative care management of late-life depression in the primary care setting. Journal of the American Medical Association. 2002;288:2836–45. doi: 10.1001/jama.288.22.2836. [DOI] [PubMed] [Google Scholar]
  • 8.Anderson LM, Adeney KL, Shinn C, et al. Community coalition-driven interventions to reduce health disparities among racial and ethnic minority populations. The Cochrane Library. 2015 doi: 10.1002/14651858.CD009905.pub2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Jones L, Wells K. Strategies for academic and clinician engagement in community-participatory partnered research. The Journal of the American Medical Association. 2007;297:407–10. doi: 10.1001/jama.297.4.407. [DOI] [PubMed] [Google Scholar]
  • 10.Chung B, Ong M, Ettner SL, et al. 12-Month Outcomes of Community Engagement Versus Technical Assistance to Implement Depression Collaborative Care: A Partnered, Cluster, Randomized, Comparative Effectiveness Trial. Annals of internal medicine. 2014;161:S23–S34. doi: 10.7326/M13-3011. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Sheehan DV, Lecrubier Y, Sheehan KH, et al. The Mini-International Neuropsychiatric Interview (MINI): The development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. Journal of Clinical Psychiatry. 1998;59:22–33. [PubMed] [Google Scholar]
  • 12.Ware JE, Sherbourne CD. The MOS 36-item short-form health survey (SF-36): I. Conceptual framework and item selection. Medical Care. 1992:473–83. [PubMed] [Google Scholar]
  • 13.Kroenke K, Strine TW, Spitzer RL, et al. The PHQ-8 as a measure of current depression in the general population. Journal of Affective Disorders. 2009;114:163–73. doi: 10.1016/j.jad.2008.06.026. [DOI] [PubMed] [Google Scholar]
  • 14.Lavori PW, Dawson R, Shera D. A multiple imputation strategy for clinical trials with truncation of patient data. Statistics in Medicine. 1995;14:1913–25. doi: 10.1002/sim.4780141707. [DOI] [PubMed] [Google Scholar]
  • 15.Pham HH, Cohen M, Conway PH. The Pioneer accountable care organization model: improving quality and lowering costs. Jama. 2014;312:1635–6. doi: 10.1001/jama.2014.13109. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

supplement

RESOURCES