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Youth Partners in Care: Depression and Quality Improvement

Youth Partners in Care: Depression & Quality Improvement

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02030782
Acronym
YPIC
Enrollment
418
Registered
2014-01-09
Start date
1999-10-31
Completion date
2003-12-31
Last updated
2014-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression

Keywords

depression, quality improvement, treatment, adolescents

Brief summary

This randomized effectiveness trial evaluates a quality improvement intervention aimed at providing access to evidence-based depression treatments (particularly cognitive-behavior therapy for depression and or pharmacotherapy) through primary care for youth ages 13-21, as compared to enhanced usual care. The major hypothesis is that the quality improvement intervention will be associated with improved outcomes, relative to enhanced usual care.

Interventions

OTHERQuality Improvement (QI) for depression

Major intervention components included a) expert leader teams who planned and implemented the intervention at each clinic, b) care managers who supported primary care clinicians with depression evaluation and management, c) access to cognitive-behavior therapy for depression within each primary care clinic, and d) patient and provider choice regarding treatment modality.

OTHERUsual Care

Usual care enhanced by provider education regarding depression evaluation and management

Sponsors

RAND
CollaboratorOTHER
Kaiser Permanente
CollaboratorOTHER
University of Pittsburgh
CollaboratorOTHER
Venice Family Clinic
CollaboratorOTHER
Agency for Healthcare Research and Quality (AHRQ)
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
13 Years to 21 Years
Healthy volunteers
No

Inclusion criteria

* Met either of two criteria: 1) endorsed stem items for major depression or dysthymia from the 12-month Composite International Diagnostic Interview(CIDI-12,2.1) modified slightly to conform to diagnostic criteria for adolescents, 1-week or more of past-month depressive symptoms, and a total Center for Epidemiological Studies- Depression Scale(CES-D)40 score ≥ 16, or 2) CES-D score ≥ 24. * Age 13-21 * Presented at primary care clinic

Exclusion criteria

* not English-speaking * provider not in study * sibling already in study * completed eligibility screener previously

Design outcomes

Primary

MeasureTime frame
Self-reported depressive symptoms on the CES-D (Center for Epidemiologic Studies Depression Scale)6-months

Secondary

MeasureTime frameDescription
mental health related quality of life as assessed using self-report on the Medical Outcomes Study Short Form 12 Health Survey.6 months, with follow up at 12 and 18 months
satisfaction with care6 months with follow up at 12 and 18 months
Rates of mental health care, counseling/psychotherapy, and medication treatment.6-months with follow-up at 12 and 18 monthsYouth self report on the study version of the Service Assessment for Children & Adolescents provided measures of rates of mental health care(dichotomous indicator of whether any mental health treatment received), counseling/psychotherapy (dichotomous indicator of whether counseling/psychotherapy was received, number of counseling/psychotherapy sessions), and medication treatment (dichotomous indicator of whether youth received any medication treatment for mental health problems). These measures were obtained using .

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026