RecruitingNot ApplicableNCT06253676

Sensing Technologies for Maternal Depression Treatment in Low-Resource Settings


Sponsor

George Washington University

Enrollment

120 participants

Start Date

May 15, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

In certain low- and middle- income country settings, there is a disproportionate level of untreated postpartum depression that presents both acute and long-term risks to a mother's well-being. Although there is increasing willingness among health systems to involve non-specialists, such as community health workers, in the delivery of psychosocial interventions for postpartum depression, the effectiveness of these interventions has been mixed. The incorporation of digital technology, though, has the potential to improve the effectiveness of non-specialist-delivered interventions. The goal of this clinical trial is to evaluate the acceptability and clinical efficacy of the StandStrong intervention- a non-specialist, passive sensing technology-informed (i.e., digital) mental health intervention- as compared to a standard non-specialist mental health intervention among postpartum-depressed mothers in Nepal. Successful completion of the trial will contribute to the optimization of psychosocial intervention delivery for the postpartum context in low- and middle-income country settings.


Eligibility

Sex: FEMALEMin Age: 15 YearsMax Age: 45 Years

Plain Language Summary

Simplified for easier understanding

This study explores whether wearable sensors and smartphone technology can help identify and monitor depression in new mothers in low-resource settings. Researchers want to understand how digital tools can support mental health care for mothers experiencing postpartum depression, particularly in places with limited access to mental health professionals. **You may be eligible if...** - You are a mother aged 15–39 - Your baby is within the first 1,000 days of life (roughly under 3 years old) - Your depression score on the PHQ-9 questionnaire is 8 or above - You have access to a device charger at home - You plan to remain in the study area for at least 6 months **You may NOT be eligible if...** - Your PHQ-9 depression score is below 8 - You and your baby live at different addresses - You or your baby have an acute medical need or are hospitalized at the time of enrollment - You show signs of psychosis Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALProblem Management Plus (PM+)

Validated across multiple low- and middle-income country settings, PM+ is World Health Organization-developed, five-session task-sharing intervention for mild to moderate distress. Per the (manualized) intervention, trained non-specialist providers coach eligible clients to address practical problems and/or distress in their daily lives via the use of fundamental cognitive behavioral strategies (e.g., deep breathing and stress management, behavioral activation, strengthening of social support, etc.).


Locations(1)

Transcultural Psychosocial Organization Nepal

Kathmandu, Nepal

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NCT06253676


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