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Exercise and Socialization in Post-partum Depression

Post-partum Depression in Kentucky: A Community Based Intervention and a Novel AI-powered Screening Tool

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06801847
Enrollment
0
Registered
2025-01-30
Start date
2025-03-28
Completion date
2025-11-30
Last updated
2025-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Partum Depression

Brief summary

This community-engaged research project aims to address the critical need for alternative treatments of post-partum depression (PPD). The goal of this research is to investigate the efficacy of a novel 8-week intervention combing exercise with social support to reduce PPD symptoms. It is hypothesized that exercise in addition to social support will more effectively reduce PPD symptom severity compared to social support alone. By collaborating with PPD mothers, clinicians, researchers, and local fitness instructors, the researchers aim to develop an intervention that is accessible, culturally appropriate, effective, and increases treatment adherence. Additionally, the researchers will investigate if mother-infant interactions during exercise can enhance bonding, thereby reducing the detrimental effects of maternal PPD on their off-spring.

Interventions

BEHAVIORALSocialization

Socialization lasting from 30-60 minutes each session

BEHAVIORALWalking

Twice weekly walking (30 minutes)

Twice weekly moderate exercise (30 minutes)

Sponsors

Laura Peterson-Brown
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Over the age of 18 years old * Two-weeks to 12 months post-partum * EPDS over 10 * Read and Speak English * Willing to supply contact information for their clinician and consent to their clinician being contacted in the event their depression worsens.

Exclusion criteria

* Use of anti-depression medication(s) at time of enrollment * Unable to give consent * Prisoner, parolee, state probationer, or awaiting sentence for a felony conviction

Design outcomes

Primary

MeasureTime frameDescription
Change in Edinburgh Post-natal Depression Scale (EPDS) scoreBaseline, 4 weeks, 8 weeksEPDS scores range between 0 and 30. EDPS depression ranking system: * 0 to 6: No depression or minimal depression * 7 to 13: Mild depression * 14 to 19: Moderate Depression * 20 to 30: Severe Depression

Secondary

MeasureTime frameDescription
Change in Mother-Infant Bonding Questionnaire (MIBQ) scoreBaseline, 4 weeks, 8 weeksMIBQ scores are between 0 and 24. Higher score indicates poor mother-baby bonding.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026