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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02976025
Other study ID # STUDY00001294
Secondary ID 1R01MH108548-01
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date April 1, 2017
Est. completion date July 2021

Study information

Verified date April 2021
Source University of Washington
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Description:

Depression is a common and serious disorder among pregnant women but few from low income groups receive effective treatment. The highly evidence based collaborative care (CC) model for depression has been shown to work for women in pregnancy but has not been widely implemented in this population. The proposed study targets improving dissemination of the evidence based CC treatment model for pregnant and postpartum women with depression, a common disorder of the perinatal period (pregnancy and the first year following birth). Longitudinal remote consultation (LRC) is an implementation strategy that has been have shown to improve fidelity to evidence-based practices and patient outcomes for mental health innovations. The investigators believe LRC can be used with equal benefit for complex interventions such as CC. The purpose of this study is to compare two implementation strategies for Collaborative Care depression treatment: 1) standard implementation and 2) standard implementation + Longitudinal Remote Consultation (LRC). This research is being done in order to assess implementation and patient outcomes in sites receiving a standard implementation approach with and without LRC. The results of the proposed study will provide information on the benefits and relative value of ongoing consultation, such as LRC, for implementation of complex interventions like collaborative care. The proposed study will involve twenty health centers providing prenatal care which are part of the national OCHIN Network or other health center network. All sites will receive a standard implementation approach. After pre-implementation training ten of the sites will be randomly selected to receive LRC. Implementation and clinical outcomes as well as costs will be compared between the study conditions after a 12 month implementation period and a 13-21 month sustainment period. The results of the proposed study will provide critical generalizable knowledge regarding the benefits of ongoing consultation for implementation of complex interventions like collaborative care.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 20
Est. completion date July 2021
Est. primary completion date July 2021
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Patient Participants: Inclusion Criteria: - Patient participants must be perinatal women, - Age 18-45, - Receiving care at one of the 20 OCHIN or non-OCHIN health centers participating in the study and must have major depression as determined by a score of =10 on the PHQ-9 depression screener. Exclusion Criteria: - Age <18 or >45, - Male. Health Center Participating Sites: Inclusion Criteria: - Use of the shared OCHIN Epic electronic record for perinatal care or use of the secure AIMS CMTS/Caseload Tracker/spreadsheet patient registry for perinatal care and - A minimum of 50 prenatal patients annually.

Study Design


Intervention

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.
Collaborative Care
Standard collaborative care implementation training and support.

Locations

Country Name City State
United States University of Washington Seattle Washington

Sponsors (6)

Lead Sponsor Collaborator
University of Washington National Institute of Mental Health (NIMH), Ochin, Inc., Oregon Social Learning Center, University of Pennsylvania, Washington University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Cost and cost-effectiveness For a cost-benefit analysis, the investigators will use of the Cost of Implementing New Strategies (COINS) method to assess costs in the two conditions. This methodology takes advantage of the SIC-CC instrument as a costing template to map the use of resources and associated costs to these to study conditions. Costs associated with implementation in each of these conditions will be carried out for all 20 health centers included in the study. 12-month post-implementation of collaborative care
Primary Clinical depression outcomes Patient Health Questionnaire-9 (PHQ-9); level of depression symptomatology and functional impairment. 12 months post-initiation of collaborative care
Secondary Implementation outcomes To assess the degree to which sites in the two conditions complete implementation, the investigators will use the Stages of Implementation Completion tool tailored for collaborative care, SIC-CC. 12 month post-implementation of collaborative care
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