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Longitudinal Remote Consultation for Postpartum Depression (MInD-I Trial)

N/A
Waitlist Available
Led By Ian Bennett
Research Sponsored by University of Washington
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months post-initiation of collaborative care
Awards & highlights

MInD-I 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.

Eligible Conditions
  • Postpartum Depression

MInD-I Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months post-initiation of collaborative care
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 months post-initiation of collaborative care for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Clinical depression outcomes
Secondary outcome measures
Implementation outcomes
Other outcome measures
Cost and cost-effectiveness

MInD-I Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Longitudinal Remote ConsultationExperimental Treatment1 Intervention
This is the active treatment arm consisting of 10 cluster randomized health centers receiving both training in collaborative care and longitudinal remote consultation (LRC) support.
Group II: Collaborative CareActive Control1 Intervention
This comparator arm will consist of 10 cluster randomized health centers who receive training in collaborative care.

Find a Location

Who is running the clinical trial?

National Institute of Mental Health (NIMH)NIH
2,785 Previous Clinical Trials
2,689,736 Total Patients Enrolled
25 Trials studying Postpartum Depression
8,143 Patients Enrolled for Postpartum Depression
University of WashingtonLead Sponsor
1,740 Previous Clinical Trials
1,847,650 Total Patients Enrolled
1 Trials studying Postpartum Depression
40 Patients Enrolled for Postpartum Depression
OCHIN, Inc.OTHER
21 Previous Clinical Trials
8,725,085 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Remote Supervision for Implementing Collaborative Care for Perinatal Depression
Ian Bennett 2017. "Remote Supervision for Implementing Collaborative Care for Perinatal Depression". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT02976025.
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~2 spots leftby Apr 2025
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