CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 1,112 enrolled
Drug / intervention
Replicating Effective Programs plus External Facilitation +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02543840
NCT02543840N/ACompleted

Hybrid Controlled Trial to Implement Collaborative Care in General Mental Health

VA Boston Healthcare System·interventional·Posted Sep 7, 2015·Updated Jun 23, 2020

In Brief

A clinical study evaluating Replicating Effective Programs plus External Facilitation and Educational Materials for Mental Health Disorders. Completed, enrolled 1,112 participants across 1 site.

Detailed Summary

This randomized program evaluation is undertaken in conjunction with the Department of Veterans Affairs (VA) Office of Mental Health Operations (OMHO) and the Quality Enhancement Research Initiative. It is designed to answer two related questions: (1) Can an evidence-based implementation strategy using the Center for Disease Control (CDC)'s Replicating Effective Programs plus External Facilitation (REP-F) enhance the adoption of team-based care in VA General Mental Health (GMH) Clinics, and (2) Does the establishment of such teams via implementation enhance Veterans' health status, satisfaction, and perceptions of care? The model for team-based care is the evidence-based Collaborative Chronic Care Model (CCM). In conjunction with a nation-wide roll-out of the VA's Behavioral Health Interdisciplinary Program team (BHIP) initiative, the investigators have structured a randomized, controlled program evaluation to answer these questions. Specifically, using a stepped wedge design the investigators will randomize 9 VAMCs that have requested support in establishing a BHIP to 1 of 3 waves of REP-F support: immediate implementation support vs. 4-month vs. 8-month wait with dissemination of CCM materials (3 sites per wave). Fidelity and health outcome measures will be collected in a repeated measures design at 6-month intervals, and analyzed with general linear modeling.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedSep 7, 2015
Enrollment StartMar 7, 2016
Primary CompletionApr 26, 2018
TodayJul 2, 2026
Enrollment to primary: 2.1 yearsPosted 10.8 years ago

Interventions

Replicating Effective Programs plus External Facilitationother

Packaging, training and technical assistance according to the Replicating Effective Programs model plus External Facilitation

Educational Materialsother

Dissemination of educational materials on the collaborative chronic care model for 4 or 8 months prior to cross-over to REP-F