Tailored Resistance Training After Adverse Pregnancy Outcomes

Not Applicable

Not yet recruiting

• Conditions: Postpartum; Adverse Pregnancy Outcomes

• Registration Number: NCT07058818
• Lead Sponsor: University of Michigan

Brief 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.

Detailed Description

People who had APOs have a higher risk of heart disease and diabetes in the future. Resistance training might help lower risk of heart disease and diabetes in people who had APOs, but it can be difficult for postpartum people to perform exercise as they are juggling demands of a new baby and healing from pregnancy and child birth. The goal of this project is to find an exercise plan that works for individuals who recently gave birth. This study will determine whether a resistance training intervention co-designed by researchers and postpartum individuals is do-able for individuals who recently had APOs.

Participants in this trial will have height and weight measured. One exercise session, including a warm-up, resistance training, and cool-down with stretching will be completed in the School of Kinesiology at the University of Michigan. Then participants will receive an exercise program to perform over the next 4 weeks. They will receive a text or email message every day for those 4 weeks asking them to reply and tell the study team if they did the resistance training and if they did the program as it was written (as prescribed).

A few survey questions about participants mood regarding physical activity before and after exercise and belief in the ability to continue to exercise at the beginning and end of the intervention will be asked. Some questions regarding what participants thought about the marketing materials and the exercise program in general will be asked at the end of the intervention.

Study Timeline

• Status Verified: 2025-06
• Study First Submitted: 2025-06-11
• Study First Submitted QC: 2025-06-30
• Last Update Submitted: 2025-06-30
• Study First Posted: 2025-07-10
• Last Update Posted: 2025-07-10
• Study Start: 2025-09-01
• Primary Completion: 2025-12
• Study Completion: 2026-02-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: Female
• Target Recruitment: 10

Inclusion Criteria

• Had a single baby in your most recent pregnancy
• Are 18-45 years old
• Are 3-15 months postpartum
• Are not currently pregnant
• Had an adverse pregnancy outcome/medical complication in your most recent pregnancy, including preeclampsia, gestational diabetes, hypertensive disorders of pregnancy, fetal growth restriction or low birth weight baby, or preterm birth
• Your doctor told you that you are able to participate in exercise
• Can attend a visit at the University of Michigan's School of Kinesiology Building
• Are willing to perform resistance exercise twice a week for 4 weeks
• Are willing to receive and respond to a daily message sharing whether you completed resistance exercise that day and completed it as recommended

Exclusion criteria:

• Had a multiple birth (twins, triplets, etc) in your most recent pregnancy
• Are <18 or >45 years old
• Are <3 months or >15 months past your last birth
• Are currently pregnant
• Are unable to exercise or have been told by a healthcare provider not to exercise
• Did not have an adverse pregnancy outcome, including preeclampsia, gestational diabetes, hypertensive disorders of pregnancy, fetal growth restriction or low birth weight baby, or preterm birth, in your most recent pregnancy
• Are unable to attend a study visit at the University of Michigan's School of Kinesiology Building
• Are not willing to perform 4 weeks of resistance training
• Are not willing to receive and send daily messages

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Adherence	4 weeks	Proportion of prescribed resistance exercise sessions completed
Compliance	4 weeks	Proportion of prescribed resistance exercise sessions completed as prescribed/directed

Secondary Outcome Measures

Name	Time	Method
Self-efficacy (assessed with validated survey)	4 weeks	Exercise self-efficacy survey
Physical activity enjoyment (assessed with validated survey)	4 weeks	Enjoyment questionnaire

Trial Locations

Locations (1)

School of Kinesiology; 🇺🇸 Ann Arbor, Michigan, United States