Remote Supervision for Implementing Collaborative Care for Perinatal Depression

NCT02976025 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2021-04-28

No results posted yet for this study

Summary

This study evaluates the impact of a longitudinal remote consultation (LRC) implementation strategy for collaborative care depression treatment among perinatal women. All participating health centers will receive training in collaborative care. Cluster randomization will be used to assign the addition of LRC to select health centers. Differences in implementation success, clinical outcomes, and costs will be compared after a 12 month implementation period and 13-21 month sustainment period.

Conditions

  • Perinatal Depression

Interventions

OTHER

Longitudinal Remote Consultation

Longitudinal Remote Consultation utilizes video conferencing to efficiently link providers to consultants who provide timely feedback and training in collaborative care. LRC will be provided in addition to standard collaborative care training and support.

OTHER

Collaborative Care

Standard collaborative care implementation training and support.

Sponsors & Collaborators

  • OCHIN, Inc.

    collaborator OTHER
  • Oregon Social Learning Center

    collaborator OTHER
  • University of Pennsylvania

    collaborator OTHER
  • Washington University School of Medicine

    collaborator OTHER
  • National Institute of Mental Health (NIMH)

    collaborator NIH
  • University of Washington

    lead OTHER

Principal Investigators

  • Ian Bennett · University of Washington

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-04-01
Primary Completion
2021-07-31
Completion
2021-07-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02976025 on ClinicalTrials.gov