Clinical Trial

Tailored Resistance Training After Adverse Pregnancy Outcomes

Study acronym: RT after APOs
Completed
View on ClinicalTrials.gov →
Summary
Approximately 7-10 postpartum people with recent adverse pregnancy outcomes (APOs: preeclampsia, gestational diabetes, hypertensive disorders of pregnancy, fetal growth restriction or low birth weight baby, or preterm birth) will be invited to complete 4 weeks of a resistance training intervention, including associated incentives, communication, and marketing materials.
Protocol Amendment History 3 changes
critical Trial completed 2026-04-09
notable Enrollment reduced: 10 -> 7 participants 2026-04-09
minor Completion moved earlier: 2026-05 -> 2026-03-07 2026-04-09
Trial Details
NCT Number NCT07058818
Lead Sponsor University of Michigan
Collaborators: Women's Health Innovation Fund
Conditions Postpartum, Adverse Pregnancy Outcomes
Enrollment 7 participants
Start Date 2026-01-08
Primary Completion 2026-03-07 (estimated)
Study Completion 2026-03-07 (estimated)
Updated on ClinicalTrials.gov 2026-04-08