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Outcomes for Youths From Racial-Ethnic Minority Groups in a Quality Improvement Intervention for Depression Treatment
Victoria K. Ngo, Ph.D.; Joan R. Asarnow, Ph.D.; Jane Lange, M.S.; Lisa H. Jaycox, Ph.D.; Margaret M. Rea, Ph.D.; Christopher Landon, M.D.; Lingqi Tang, Ph.D.; Jeanne Miranda, Ph.D.
Psychiatric Services 2009; doi: 10.1176/appi.ps.60.10.1357
View Author and Article Information

Dr. Ngo and Dr. Jaycox are affiliated with RAND Corporation, 1776 Main St., Santa Monica, CA 90407 (e-mail: vngo@rand.org). Dr. Asarnow, Dr. Tang, and Dr. Miranda are with the Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles. Ms. Lange is with the Department of Biostatistics, University of Washington, Seattle. Dr. Rea is with the School of Medicine, University of California, Davis, Sacramento. Dr. Landon is with Ventura County Medical Center, Ventura, California.

Objective: This study examined racial-ethnic differences in the impact of the Youth Partners in Care quality improvement intervention. The intervention was designed to improve access to evidence-based depression care, primarily cognitive-behavioral therapy and medication, through primary care. Previous analyses have shown that the quality improvement intervention was associated with improved depression and quality-of-life outcomes at the end of the six-month intervention period. Methods: A randomized controlled trial comparing quality improvement and usual care for youths from diverse racial-ethnic groups from five health care organizations, including managed care, the public sector, and academic center clinics, was conducted. Depressed youths (N=325), who self-identified as black (N=59), Latino (N=224), and white (N=42), aged 13–21 years, were included in these analyses. To evaluate intervention effects within racial-ethnic groups, regression models were constructed, which adjusted for baseline and study site variation in depression symptoms, mental health status, satisfaction with mental health care, and mental health service utilization. Results: Differential intervention effects were found across racial-ethnic groups. Black youths in the intervention group experienced significant reductions in depression symptoms and had higher rates of use of specialty mental health care at the six-month follow-up. Among Latino youths, the intervention was associated with significantly greater satisfaction with care. Intervention effects were weak among white youths. Conclusions: Quality improvement interventions may help to reduce disparities in mental health care for youths from racial-ethnic minority groups. (Psychiatric Services 60: 1357–1364, 2009)

Abstract Teaser
Figures in this Article

Racial-ethnic diversity among children in the United States is increasing. In 2000 children from minority groups accounted for 39% of the population under 18 (1), and the proportion is projected to rise to 48% in the next quarter century (2). Increasingly, evidence-based mental health interventions have been found effective for youths from ethnic minority groups (3,4). Nevertheless, these children are less likely than white youths to receive high-quality mental health services (5,6) and more likely to leave treatment prematurely (7).Strategies for addressing mental health disparities among youths are needed, because untreated depression in this population is associated with suicide, school dropout, pregnancy, substance abuse, and depression in adulthood (8,9,10,11,12,13,14).

A promising approach to address health disparities has been to improve the quality of mental health services provided in primary care settings (15,16,17,18), because primary care is a gateway to mental health care for individuals from racial-ethnic minority groups. Quality improvement interventions in primary care settings aimed at improving access to evidence-based depression treatments have been found to be more effective than usual care for diverse groups of depressed adults (16,17,19), elderly persons (20), and adolescents (21). In the Partners in Care study of adults, intervention effects on clinical outcomes were greatest for blacks and Latinos (22). The quality improvement interventions significantly decreased the likelihood of participant reports of probable depression at six- and 12-month follow-ups for blacks and Latinos in the study, whereas their white counterparts showed no such difference (22). In the IMPACT Study of elderly adults, all racial-ethnic groups (blacks, Latinos, and whites) in the quality improvement condition showed greater rates of depression care, lower depression severity, and less health-related functional impairments than patients in the usual care group (23).

No study has examined racial-ethnic differences in the impact of quality improvement interventions in an adolescent population. Youth Partners in Care is the first and largest study to evaluate a quality improvement intervention for depression among youths that was delivered in primary care settings. Results indicated that quality improvement aimed at increasing rates of evidence-based depression care (primarily cognitive-behavioral therapy [CBT] and medication) was associated with improved depression and quality-of-life outcomes, satisfaction with care, and increased rates of care—primarily counseling (21). The study reported here examined the differential impact of the quality improvement intervention among racial-ethnic groups, with the overall goal of informing efforts to decrease mental health disparities and improve outcomes for youths from minority groups. We hypothesized that racial-ethnic differences similar to those found in studies of adults would result from the quality improvement intervention, such that black and Latino youths would report greater improvement in depression symptoms than their white counterparts six months after the intervention.

We used data from Youth Partners in Care, a multisite randomized effectiveness trial conducted between 1999 and 2003 that compared a quality improvement intervention with usual care. The study protocol was approved by the institutional review boards of all participating organizations. All participants over the age of 18 and legal guardians for youths under age 18 provided informed consent, with youths under age 18 providing assent. The methodology, including study design, data collection procedures, and measures, has been described in detail elsewhere (21,24).

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Sample

Following common adolescent medicine practices (25), we defined adolescence broadly, extending into the transitional-age period. Youths aged 13 through 21 who presented at clinics for a primary care visit were screened. Patients completed brief self-administered screening questionnaires in the clinics. Enrollment eligibility was based on meeting either of two criteria. First, the youth had to endorse "stem items" for major depression or dysthymia from the 12-month Composite International Diagnostic Interview (CIDI) (26) and have a total score of 16 or higher on the Center for Epidemiological Studies Depression Scale (CES-D) (16). (For adolescents who reported having experienced depression symptoms for at least one week in the past month, the CIDI was modified slightly to conform to DSM-IV diagnostic criteria.) Second, the youth had to have a CES-D score of 24 or higher (27,28). Youths were excluded if they did not speak English, had providers who were not in the study, or had a sibling already in the study. Participants' racial-ethnic group was based on self-report; they were provided a list of racial-ethnic groups and could endorse more than one.

Participants were randomly assigned to either the quality improvement or usual care condition. Staff members who conducted the screening and enrollment were blind to randomization status and did not conduct the assessment. The median time delay between screening and random assignment was 21 days. Among the 418 youths enrolled, 344 (82%) completed the six-month follow-up assessment. Follow-up rates did not differ significantly across conditions (171 youths, or 81%, in the quality improvement intervention and 173 youths, or 84%, in usual care). In the analyses for this study, we included only youths classified as Latino, black, or white, which yielded a sample of 325 youths at six-month follow-up.

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Usual care and intervention conditions

The usual care condition was enhanced by giving primary care providers training and educational materials on depression evaluation and treatment (21). Participants assigned to usual care had access to usual care at the site, but they did not have access to providers who were trained in a quality improvement model that included CBT or care management services.

The quality improvement intervention included expert-led teams at each site that adapted and implemented the intervention; master's- or doctoral-level care managers who supported primary care providers with patient evaluation, education, medication, and psychosocial treatment and linkage to specialty mental health services; training for care managers in manualized CBT for depression; and patient and provider choice of treatment modalities (CBT, medication, combined CBT and medication, care management follow-up, and referral). Primary care providers were informed of patient participation in the study only if the participant was in the quality improvement condition.

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Cultural modifications

Youth Partners in Care strategies for addressing cultural issues in the intervention included a focus on training staff on cultural sensitivity issues, tailoring examples to fit the cultural context of each youth and family, ensuring when possible that the care manager and participant spoke the same language (3,21,29), and providing consultation with cultural researchers. We encouraged care managers to attend to cultural issues. For example, the traditional Latino view is that important decisions, including those involving mental health care, should be made by the father, and youths may resent this tradition. The care managers were also reminded of the importance of cultural concepts, such as "simpatico"—warm and caring interactions that emphasize understanding and concern for the welfare of the entire family.

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Data collection

Baseline and six-month follow-up assessments were conducted by interviewers from the Battelle Survey Research Institute who were blind to group assignment. Interviews with the youths assessed clinical characteristics, including depression, posttraumatic stress disorder (PTSD), substance abuse, and problem behaviors, including suicidal behaviors. To diagnose depression, the CIDI was used at baseline; the CES-D was administered only at the six-month follow-up. To capture a broad range of youth depression, investigators diagnosed major depression or dysthymia and screened for other comorbidities, including mania, PTSD, and substance abuse. The Mental Health Index-5 (MHI-5) (30) was also used to measure general emotional distress at baseline. In addition to clinical characteristics, the six-month interview assessed demographic characteristics, mental health-related quality of life, satisfaction with mental health care, and mental health service use in the past six months.

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Measures

The CES-D is a 20-item self-report measure of depression symptoms during the past week (27). The MHI-5 (30) is a five-item general mental health measure constructed from items that best predict a summary score from the 38-item Mental Health Inventory. Items assess symptoms of depression and anxiety, loss of behavioral or emotional control, and psychological well-being in the previous month. The Youth Self Report (YSR) is a self-report questionnaire designed for assessment of adolescents' problems (31). The externalizing subscale was used to assess aggressive and delinquent behavior. A single YSR item (suicidal ideation) was also used to assess suicide risk. The Problem Oriented Screening Instrument for Teenagers is a brief dichotomous screening tool for identification of ten functional problem areas among teenagers (32). We used the substance use-abuse subscale (13 items) to identify substance use. A positive response to even one question is considered to reflect a moderate risk of a significant substance abuse problem.

The Primary Care PTSD Screen is a four-item screen (33). Endorsement of any symptom indicates risk for PTSD. The mental component summary scale (MCS-12) (34) is a 12-item self-report measure derived from the Medical Outcomes Study 36-Item Short-Form Health Survey. It is thus a short-form generic measure that assesses quality of life and functioning. The scale is scored with norm-based methods and has a mean of 50 and a standard deviation of 10 in the general U.S. population. Thus all scores above and below 50 are above and below the average in the population. Higher scores indicate better health-related quality of life and functioning.

Satisfaction with mental health care was assessed with two items that used a 5-point scale ranging from 1, very dissatisfied, to 5, very satisfied (35). Mental health service utilization was assessed by items about receipt of psychotherapy or counseling; mental health specialty services from a psychologist, psychiatrist, or therapist; mental health treatment by primary care provider; and medication for mental health problems (21). The respondent was also asked to report the frequency of psychotherapy visits within the past six months. [A list of items used to assess mental health service utilization is available as an online supplement to this article at ps.psychiatryonline.org.]

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Data analysis

We examined the association between baseline demographic and clinical characteristics and racial-ethnic group. We used chi square tests for categorical variables and analysis of covariance (ANCOVA) for continuous variables. Because the study was not powered to detect differential intervention effects across racial-ethnic groups, we focused on intervention effects within each racial-ethnic group (blacks, Latinos, and whites). To increase power, we reallocated the 47 mixed-race participants using the following criteria. Individuals who self-identified as Latino but not as black were classified as Latino (N=21). (These individuals may also have endorsed other racial-ethnic groups but not black on the list provided). Those who self-identified as black or "other" but not Latino were reclassified as black (N=14). Those who self-identified as both Latino and black and reported that Spanish was spoken at home were classified as Latino (N=6), because use of the Spanish language is strongly associated with first-generation immigrant status, a lower level of acculturation, and Latino identity (36,37). Those who self-identified as both black and Latino and who reported that Spanish was not spoken at home were classified as black (N=6), because among blacks who do not speak Spanish at home, black identity and phenotype in the United States are salient and predictive of a wide variety of outcomes, including socioeconomic status, health status, and educational attainment (38,39,40).

With these criteria, the baseline sample included 390 participants (76 blacks, 261 Latinos, and 53 whites). The six-month follow-up sample included 325 participants (59 blacks, 224 Latinos, and 42 whites). We conducted analyses before and after reallocation of mixed-race participants and found similar results.

We conducted intent-to-treat analyses. Data for participants were analyzed according to the experimental group to which they were assigned regardless of whether they received treatment or used study resources such as care management. We fitted ANCOVA models for continuous outcomes (CES-D score, MCS-12 score, and satisfaction with mental health care) and logistic regression models for dichotomous outcomes (service use). Independent variables included intervention status, racial-ethnic group, and interactions between intervention status and racial-ethnic group, and analyses adjusted for the baseline measure for the same outcome and study site. Two-step modeling was used by first fitting random intercept models for sites and then including the estimated random effects for sites in the final ANCOVA model (41). For analysis of CES-D scores at follow-up, we used the baseline MHI-5 score as a covariate because the CES-D was not used at baseline. CES-D and MHI-5 scores were highly correlated at follow-up (r=.78, p<.001); therefore, the baseline MHI-5 score was used to control for baseline CES-D score.

To show effect sizes, we present adjusted group means and differences as well as odds ratios by intervention and racial-ethnic groups, adjusted for the baseline measure (42). We used nonresponse weighting (43,44) to address missing data for 18% of patients who did not complete the six-month assessment. The objective of nonresponse weighting is to extrapolate from the observed six-month sample to the original intent-to-treat sample. Nonresponse weights were constructed by fitting logistic regression models to predict follow-up status from baseline clinical and demographic characteristics. Separate models were fitted for each intervention group. The reciprocal of the predicted follow-up probability was used as the nonresponse weight for each participant. Intent-to-treat analyses for intervention effects, weighted by nonresponse weights, were conducted by using survey commands in SUDAAN, version 9 (45). Weighted and unweighted analyses yielded similar results, and where results varied, the differences are noted below.

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Racial-ethnic group differences at baseline

Baseline characteristics of the sample are presented by race and ethnicity in Table 1. No significant baseline differences were found between racial-ethnic groups in depression and other mental health indicators, including externalizing behavior, PTSD, substance use, and suicidal behavior. However, some differences in demographic characteristics were found. Specifically, blacks were less likely to have at least one parent employed, a greater proportion of Latinos were bilingual, and Latinos were more likely to have immigrant parents. Consistent with the literature indicating less access to high-quality mental health care for individuals from racial-ethnic minority groups (4,5), use of mental health services was significantly higher among whites as measured by provider type (mental health specialty care and mental health treatment by primary care providers), service type (counseling and medication), and frequency of counseling sessions at baseline. No significant racial-ethnic differences in mental health indicators were found between the quality improvement group and the usual care group at baseline.

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Intervention effects by racial-ethnic group

Results showed a significant reduction in depression symptoms among blacks in the intervention group. Among Latinos in the intervention group the only significant improvement was in satisfaction. No intervention effects were found for whites. We did not observe a statistically significant interaction between intervention status and racial-ethnic group in any model.

As shown in Table 2, intervention effects were significant for black youths, who experienced a large reduction in depression symptoms as a result of the quality improvement intervention (p=.001) compared with the other two groups. No intervention effects on depression symptoms were found for Latino or white youths.

No significant racial-ethnic differences in mental health-related quality of life were observed between the intervention and usual care groups. In terms of satisfaction with mental health care, intervention effects were significant only for Latinos (p=.02).

At the six-month follow-up we found that the intervention effects noted above were associated with increased rates of mental health service use, primarily for counseling and psychotherapy (Table 3). Among blacks, youths in the intervention group had greater odds of receiving any counseling (37% compared with 18% of blacks in the usual care group) and specialty mental health care (42% and 9%). No differences between the intervention and usual care groups were found for medication use or mental health treatment by a primary care clinician. The total amount of psychotherapy visits reported by black patients also significantly increased as a function of the quality improvement intervention. Findings were similar for Latino patients, with significant increases in the intervention group in the proportion using specialty mental health care (28% compared with 17% in the usual care group) and a trend toward significantly greater use of counseling (p=.07). No significant effects were found in rates of medication use or in any mental health care by primary care provider. In contrast, no significant intervention effects were found for whites on the variables related to mental health service use, although the increase in number of psychotherapy visits by those in the intervention group approached significance (p=.055).

Findings from Youth Partners in Care, the largest effectiveness trial to evaluate quality improvement in the treatment of depression among youths, support the value of quality improvement for addressing racial-ethnic disparities in health care utilization and outcomes. This is the first practical trial demonstrating that improvements in the quality of depression treatment for youths in primary care settings can improve depression outcomes and rates of use of mental health care (primarily psychotherapy and counseling), particularly among black youths. Although similar trends were found for Latinos, the intervention effect on depression outcomes was strongest for blacks.

Our results also suggest that the intervention may have operated through different mechanisms across racial-ethnic groups. Among Latinos the availability of intervention resources resulted in more satisfaction among youths and greater use of specialty mental health treatment, even though the intervention effect on depression symptoms was weak. These findings suggest that the intervention may have had a different impact on Latino youths than on white or black youths, underscoring the need to clarify racial-ethnic differences in outcomes. Research should further address differential pathways to care and strategies for improving outcomes for various racial-ethnic minority groups.

It is interesting that no significant intervention effects were found among whites, although a marginal improvement in the frequency of psychotherapy visits was noted. Because more white youths were already receiving mental health treatment at baseline, the Youth Partners in Care intervention algorithm would have encouraged "watchful waiting" by the primary care providers to monitor mental health status and treatment adherence among youths, with coordination of care between primary care providers and mental health providers. Furthermore, as might be expected because of the higher rates of mental health care utilization at baseline, whites in the usual care condition may have shown improvement during the intervention period. Thus the weaker intervention effects among whites may result from earlier access to mental health care, which may have led to comparable depression outcomes among the quality improvement and usual care groups at six-month follow-up. This would be consistent with results from adult studies suggesting that quality improvement interventions are particularly needed and powerful among persons from minority groups.

This study has several limitations. Sites were not selected at random. Although analyses adjusted for site, race-ethnicity was not equally distributed across sites and different effects might have emerged in different racial-ethnic groups. Additional research with greater power to detect effects on racial-ethnic groups is needed to further clarify the needs of various racial-ethnic groups and optimal approaches for addressing mental health needs of youths from diverse backgrounds. It is also possible that the null finding for whites could be related to the small sample size, which resulted in low power to detect differences for this group in particular. In addition, outcomes were based on youth self-report. Given our sample size and lack of detail about services provided by care managers and primary care providers, results are preliminary and clearly need to be replicated in larger samples.

The Youth Partners in Care results are consistent with findings from large quality improvement studies of depressed adult and elderly populations, in which quality improvement interventions benefited persons from racial-ethnic minority groups more than their white counterparts. Building on prior demonstrations of improved outcomes from quality improvement interventions for adult and late-life depression (16,17,19), our results indicate that this approach can be adapted successfully for younger populations from diverse backgrounds and can yield similar outcomes. Both Youth Partners in Care and the adult Partners in Care (16) achieved a difference of roughly 10 percentage points in the proportion of patients whose CES-D scores indicated clinically significant depression. Because evidence supporting depression treatments is less established for racial-ethnic minority groups, it is significant that similarly designed quality improvement interventions have been effective for youths from racial-ethnic minority groups, for adults, and for elderly persons (22,23). This has clear implications for improving racial-ethnic disparities in mental health care.

The results of this study offer hope that quality improvement interventions in primary health care settings can close the gap in depression care for youths from underserved racial-ethnic minority groups. Future research and service development are needed to clarify optimal strategies for meeting needs and improving mental health outcomes among the diverse youths in our nation.

Primary support for the Youth Partners in Care study was provided by grant HS09908 from the Agency for Healthcare Research and Quality. Additional support for the study reported here was provided by grants MH073517:04A1, 1P30MH082760–01, P30MH068639, and 2P20MD000182-06 from the National Institute of Mental Health; grant 2P30AG021684-06 from the National Center on Minority Health and Health Disparities; grant 2P30AG021684-06 from the National Institute on Aging; and the John D. and Catherine T. MacArthur Foundation. The authors thank the participating sites and their clinicians, staff, and patients, whose commitment to the project made the study possible.

Dr. Asarnow has provided consultation on CBT and has received unrestricted research funding from Philip Morris USA, Inc. The other authors report no competing interests.

O'Hare WP: The Child Population: First Data From the 2000 Census. A Kids Count/Population Reference Bureau Report on Census 2000. Baltimore, Annie E Casey Foundation, 2001
 
Census 2000 Redistricting (Public Law 94–171) Summary File. Washington, DC, US Census Bureau, 2001
 
Miranda J, Bernal G, Lau A, et al: The state of the science for psychosocial interventions for ethnic minorities. Annual Review of Clinical Psychology 1:113–142, 2005
 
Huey S, Polo A: Evidence-based psychosocial treatments for ethnic minority youth. Journal of Clinical Child and Adolescent Psychology 37:262–301, 2008
 
Elster A, Jarosik J, VanGeest J, et al: Racial and ethnic disparities in health care for adolescents: a systematic review of the literature. Archives of Pediatric Adolescent Medicine 157:867–874, 2003
 
Shaffer D, Fisher P, Dulcan M, et al: The NIMH Diagnostic Interview Schedule for Children Version 2.3 (DISC-2.3): description, acceptability, prevalence rates, and performance in the MECA Study—Methods for the Epidemiology of Child and Adolescent Mental Health Disorders Study. Journal of the American Academy of Child and Adolescent Psychiatry 35:865–877, 1996
 
Bui KV, Takeuchi DT: Ethnic minority adolescents and the use of community mental health care services. American Journal of Community Psychology 20:403–417, 1992
 
Asarnow JR, Ben-Meir S: Children with schizophrenia spectrum and depressive disorders: a comparative study of premorbid adjustment, onset pattern and severity of impairment. Journal of Child Psychology, Psychiatry and Allied Disciplines 29:477–488, 1988
 
Hammen CA: Cognitive approaches to depression in children: current findings and new directions; in Advances in Clinical Child Psychology. Edited by Lahey BB, Kazdin AE. New York, Plenum, 1990
 
Kandel DB, Davies M: Adult sequelae of adolescent depressive symptoms. Archives of General Psychiatry 43:255–262, 1986
 
Kessler RC, Foster CL, Saunders WB, et al: Social consequences of psychiatric disorders: I. educational attainment. American Journal of Psychiatry 152:1026–1032, 1995
 
Kovacs M, Goldston D: Cognitive and social cognitive development of depressed children and adolescents. Journal of the American Academy of Child and Adolescent Psychiatry 30:388–392, 1991
 
Rao U, Ryan ND, Birmaher B, et al: Unipolar depression in adolescents: clinical outcome in adulthood. Journal of the American Academy of Child and Adolescent Psychiatry 34:566–578, 1995
 
Ryan ND, Puig-Antich J, Ambrosini P, et al: The clinical picture of major depression in children and adolescents. Archives of General Psychiatry 44:854–861, 1987
 
Mental Health: Culture, Race and Ethnicity: A Supplement to Mental Health: A Report of the Surgeon General. Rockville, Md, Substance Abuse and Mental Health Services Administration, Center for Mental Health Services, 2001
 
Wells KB, Sherbourne CD, Schoenbaum M, et al: Impact of disseminating quality improvement programs for depression in managed primary care: a randomized controlled trial. JAMA 283:212–220, 2000
 
Wells KB, Sherbourne CD, Schoenbaum M, et al: Five-year impact of quality improvement for depression: results of a group-level randomized controlled trial. Archives of General Psychiatry 61:378–386, 2004
 
Wells KB, Sherbourne C, Duan N, et al: Quality improvement for depression in primary care: do patients with subthreshold depression benefit in the long run? American Journal of Psychiatry 162:1149–1157, 2005
 
Katon W, Von Korff M, Lin EH, et al: Stepped collaborative care for primary care patients with persistent symptoms of depression: a randomized trial. Archives of General Psychiatry 56:1009–1115, 1999
 
Unützer J, Katon W, Callahan CM, et al: Collaborative care management of late-life depression in the primary care setting: a randomized controlled trial. JAMA 288:2836–2845, 2002
 
Asarnow JR, Jaycox LH, Duan N, et al: Effectiveness of a quality improvement intervention for adolescent depression in primary care clinics: a randomized controlled trial. JAMA 293:311–319, 2005
 
Miranda J, Duan N, Sherbourne C, et al: Can quality improvement interventions improve care and outcomes for depressed minorities? Results of a randomized controlled trial. Health Services Research 38:613–630, 2003
 
Areàn PA, Ayalon L, Hunkeler E, et al: Improving depression care for older, minority patients in primary care. Medical Care 43:381–390, 2005
 
Asarnow J, McKowen J, Jaycox L: Improving care for depression: integrating evidence-based depression treatment within primary care services; in Treatment of Adolescent Depression. Edited by Essau CA. London, Oxford University Press, 2009
 
Society for Adolescent Medicine: A position statement of the Society for Adolescent Medicine. Journal of Adolescent Health 16:413, 1995
 
Composite International Diagnostic Interview (CIDI) Core Version 2.1 Interviewer's Manual. Geneva, World Health Organization, 1997
 
Radloff LS: The CES-D scale: a self report depression scale for research in the general population. Applied Psychological Measurement 1:385–401, 1977
 
Clarke GN, Hawkins W, Murphy M, et al: Targeted prevention of unipolar depressive disorder in an at-risk sample of high school adolescents: a randomized trial of group cognitive intervention. Journal of the American Academy of Child Adolescent Psychiatry 34:312–321, 1995
 
Guidelines on Multicultural Education, Training, Research, Practice, and Organizational Change for Psychologists. Washington, DC, American Psychological Association, 2002. Available at www.apa.org/pi/multiculturalguidelines
 
Ware JE, Sherbourne CD: The MOS 36-item Short-Form Health Survey (SF-36): I. conceptual framework and item selection. Medical Care 30:473–483, 1992
 
Achenbach TM: Manual for the Youth Self Report and 1991 Profile. Burlington, University of Vermont, Department of Psychiatry, 1997
 
Rahdert E: The Adolescent Assessment and Referral System Manual. DHHS pub no (ADM) 91-1735. Rockville, Md, National Institute on Drug Abuse, 1991
 
Prins A, Ouimette PC, Kimerling R, et al: The Primary Care PTSD screen (PC-PTSD). Primary Care Psychiatry 9:9–14, 2003
 
Ware JE Jr, Kosinski M, Keller SD: A 12-Item Short-Form Health Survey: construction of scales and preliminary tests of reliability and validity. Medical Care 34:220–233, 1996
 
Edlund MJ, Young AS, Kung FY, et al: Does satisfaction reflect the technical quality of mental health care? Health Services Research 38:631–645, 2003
 
Cruz TH, Marshall SW, Bowling JM, et al: The validity of a proxy acculturation scale among US Hispanics. Hispanic Journal of Behavioral Sciences 30:425–446, 2008
 
Deyo RA, Diehl AK, Hazuda H, et al: A simple language-based acculturation scale for Mexican Americans: validation and application to health care research. American Journal of Public Health 75:51–55, 1985
 
Keith VM, Herring C: Skin tone and stratification in the black community. American Journal of Sociology 97:760–779, 1991
 
Health United States 2006, With Chartbook on Trends in the Health of Americans. Hyattsville, Md, National Center for Health Statistics, 2006
 
Healthy People 2010 Midcourse Review. Washington, DC, US Department of Health and Human Services, 2005. Available at www.healthypeople.gov/publications
 
Raudenbush SW, Bryk AS: Hierarchical Linear Models: Applications and Data Analysis Methods, 2nd ed. Newbury Park, Calif, Sage, 2003
 
Graubard B, Korn EL: Predictive margins with survey data. Biometrics 55:652–659, 1999
 
Brick JM, Kalton G: Handling missing data in survey research. Statistical Methods of Medical Research 5:215–238, 1996
 
Kalton G: Handling wave nonresponse in panel surveys. Journal of Official Statistics 2:303–314, 1986
 
SUDAAN Language Manual, release 9.0. Research Triangle Park, NC, Research Triangle Institute, 2004
 
Table 1  Characteristics of the baseline sample of 390 youths participating in the Youth Partners in Care study, by racial-ethnic group
Table 2  Outcome measures at the six-month follow-up among 325 youths assigned to the quality improvement intervention or usual care, by racial-ethnic group
Table 3  Mental health service use during the six-month follow-up period among 325 youths assigned to the quality improvement intervention or usual care, by racial-ethnic group
Table 1  Characteristics of the baseline sample of 390 youths participating in the Youth Partners in Care study, by racial-ethnic group
Table 2  Outcome measures at the six-month follow-up among 325 youths assigned to the quality improvement intervention or usual care, by racial-ethnic group
Table 3  Mental health service use during the six-month follow-up period among 325 youths assigned to the quality improvement intervention or usual care, by racial-ethnic group
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References

O'Hare WP: The Child Population: First Data From the 2000 Census. A Kids Count/Population Reference Bureau Report on Census 2000. Baltimore, Annie E Casey Foundation, 2001
 
Census 2000 Redistricting (Public Law 94–171) Summary File. Washington, DC, US Census Bureau, 2001
 
Miranda J, Bernal G, Lau A, et al: The state of the science for psychosocial interventions for ethnic minorities. Annual Review of Clinical Psychology 1:113–142, 2005
 
Huey S, Polo A: Evidence-based psychosocial treatments for ethnic minority youth. Journal of Clinical Child and Adolescent Psychology 37:262–301, 2008
 
Elster A, Jarosik J, VanGeest J, et al: Racial and ethnic disparities in health care for adolescents: a systematic review of the literature. Archives of Pediatric Adolescent Medicine 157:867–874, 2003
 
Shaffer D, Fisher P, Dulcan M, et al: The NIMH Diagnostic Interview Schedule for Children Version 2.3 (DISC-2.3): description, acceptability, prevalence rates, and performance in the MECA Study—Methods for the Epidemiology of Child and Adolescent Mental Health Disorders Study. Journal of the American Academy of Child and Adolescent Psychiatry 35:865–877, 1996
 
Bui KV, Takeuchi DT: Ethnic minority adolescents and the use of community mental health care services. American Journal of Community Psychology 20:403–417, 1992
 
Asarnow JR, Ben-Meir S: Children with schizophrenia spectrum and depressive disorders: a comparative study of premorbid adjustment, onset pattern and severity of impairment. Journal of Child Psychology, Psychiatry and Allied Disciplines 29:477–488, 1988
 
Hammen CA: Cognitive approaches to depression in children: current findings and new directions; in Advances in Clinical Child Psychology. Edited by Lahey BB, Kazdin AE. New York, Plenum, 1990
 
Kandel DB, Davies M: Adult sequelae of adolescent depressive symptoms. Archives of General Psychiatry 43:255–262, 1986
 
Kessler RC, Foster CL, Saunders WB, et al: Social consequences of psychiatric disorders: I. educational attainment. American Journal of Psychiatry 152:1026–1032, 1995
 
Kovacs M, Goldston D: Cognitive and social cognitive development of depressed children and adolescents. Journal of the American Academy of Child and Adolescent Psychiatry 30:388–392, 1991
 
Rao U, Ryan ND, Birmaher B, et al: Unipolar depression in adolescents: clinical outcome in adulthood. Journal of the American Academy of Child and Adolescent Psychiatry 34:566–578, 1995
 
Ryan ND, Puig-Antich J, Ambrosini P, et al: The clinical picture of major depression in children and adolescents. Archives of General Psychiatry 44:854–861, 1987
 
Mental Health: Culture, Race and Ethnicity: A Supplement to Mental Health: A Report of the Surgeon General. Rockville, Md, Substance Abuse and Mental Health Services Administration, Center for Mental Health Services, 2001
 
Wells KB, Sherbourne CD, Schoenbaum M, et al: Impact of disseminating quality improvement programs for depression in managed primary care: a randomized controlled trial. JAMA 283:212–220, 2000
 
Wells KB, Sherbourne CD, Schoenbaum M, et al: Five-year impact of quality improvement for depression: results of a group-level randomized controlled trial. Archives of General Psychiatry 61:378–386, 2004
 
Wells KB, Sherbourne C, Duan N, et al: Quality improvement for depression in primary care: do patients with subthreshold depression benefit in the long run? American Journal of Psychiatry 162:1149–1157, 2005
 
Katon W, Von Korff M, Lin EH, et al: Stepped collaborative care for primary care patients with persistent symptoms of depression: a randomized trial. Archives of General Psychiatry 56:1009–1115, 1999
 
Unützer J, Katon W, Callahan CM, et al: Collaborative care management of late-life depression in the primary care setting: a randomized controlled trial. JAMA 288:2836–2845, 2002
 
Asarnow JR, Jaycox LH, Duan N, et al: Effectiveness of a quality improvement intervention for adolescent depression in primary care clinics: a randomized controlled trial. JAMA 293:311–319, 2005
 
Miranda J, Duan N, Sherbourne C, et al: Can quality improvement interventions improve care and outcomes for depressed minorities? Results of a randomized controlled trial. Health Services Research 38:613–630, 2003
 
Areàn PA, Ayalon L, Hunkeler E, et al: Improving depression care for older, minority patients in primary care. Medical Care 43:381–390, 2005
 
Asarnow J, McKowen J, Jaycox L: Improving care for depression: integrating evidence-based depression treatment within primary care services; in Treatment of Adolescent Depression. Edited by Essau CA. London, Oxford University Press, 2009
 
Society for Adolescent Medicine: A position statement of the Society for Adolescent Medicine. Journal of Adolescent Health 16:413, 1995
 
Composite International Diagnostic Interview (CIDI) Core Version 2.1 Interviewer's Manual. Geneva, World Health Organization, 1997
 
Radloff LS: The CES-D scale: a self report depression scale for research in the general population. Applied Psychological Measurement 1:385–401, 1977
 
Clarke GN, Hawkins W, Murphy M, et al: Targeted prevention of unipolar depressive disorder in an at-risk sample of high school adolescents: a randomized trial of group cognitive intervention. Journal of the American Academy of Child Adolescent Psychiatry 34:312–321, 1995
 
Guidelines on Multicultural Education, Training, Research, Practice, and Organizational Change for Psychologists. Washington, DC, American Psychological Association, 2002. Available at www.apa.org/pi/multiculturalguidelines
 
Ware JE, Sherbourne CD: The MOS 36-item Short-Form Health Survey (SF-36): I. conceptual framework and item selection. Medical Care 30:473–483, 1992
 
Achenbach TM: Manual for the Youth Self Report and 1991 Profile. Burlington, University of Vermont, Department of Psychiatry, 1997
 
Rahdert E: The Adolescent Assessment and Referral System Manual. DHHS pub no (ADM) 91-1735. Rockville, Md, National Institute on Drug Abuse, 1991
 
Prins A, Ouimette PC, Kimerling R, et al: The Primary Care PTSD screen (PC-PTSD). Primary Care Psychiatry 9:9–14, 2003
 
Ware JE Jr, Kosinski M, Keller SD: A 12-Item Short-Form Health Survey: construction of scales and preliminary tests of reliability and validity. Medical Care 34:220–233, 1996
 
Edlund MJ, Young AS, Kung FY, et al: Does satisfaction reflect the technical quality of mental health care? Health Services Research 38:631–645, 2003
 
Cruz TH, Marshall SW, Bowling JM, et al: The validity of a proxy acculturation scale among US Hispanics. Hispanic Journal of Behavioral Sciences 30:425–446, 2008
 
Deyo RA, Diehl AK, Hazuda H, et al: A simple language-based acculturation scale for Mexican Americans: validation and application to health care research. American Journal of Public Health 75:51–55, 1985
 
Keith VM, Herring C: Skin tone and stratification in the black community. American Journal of Sociology 97:760–779, 1991
 
Health United States 2006, With Chartbook on Trends in the Health of Americans. Hyattsville, Md, National Center for Health Statistics, 2006
 
Healthy People 2010 Midcourse Review. Washington, DC, US Department of Health and Human Services, 2005. Available at www.healthypeople.gov/publications
 
Raudenbush SW, Bryk AS: Hierarchical Linear Models: Applications and Data Analysis Methods, 2nd ed. Newbury Park, Calif, Sage, 2003
 
Graubard B, Korn EL: Predictive margins with survey data. Biometrics 55:652–659, 1999
 
Brick JM, Kalton G: Handling missing data in survey research. Statistical Methods of Medical Research 5:215–238, 1996
 
Kalton G: Handling wave nonresponse in panel surveys. Journal of Official Statistics 2:303–314, 1986
 
SUDAAN Language Manual, release 9.0. Research Triangle Park, NC, Research Triangle Institute, 2004
 
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