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Tailored Resistance Training After Adverse Pregnancy Outcomes

NCT07058818 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 7

Last updated 2026-04-08

No results posted yet for this study

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.

Conditions

  • Postpartum
  • Adverse Pregnancy Outcomes

Interventions

BEHAVIORAL

Resistance training

Full-body physical therapy and resistance training intervention

Sponsors & Collaborators

Principal Investigators

  • Abbi Lane, PhD · University of Michigan

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-01-08
Primary Completion
2026-03-07
Completion
2026-03-07

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07058818 on ClinicalTrials.gov