School of Kinesiology
Ann Arbor, Michigan, 48109, United States
NCT Number: NCT07058818
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.
Looking for future studies?
Notify Me18 year–45 year
Female
Interventional
Not applicable
Ann Arbor, Michigan, 48109, United States
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. An exercise session at around the midpoint of the program will be supervised by a trainer as a check point. 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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Full-body physical therapy and resistance training intervention
Time frame: 4 weeks
Proportion of prescribed resistance exercise sessions completed
Time frame: 4 weeks
Proportion of prescribed resistance exercise sessions completed as prescribed/directed
Time frame: 4 weeks
Exercise self-efficacy survey
Time frame: 4 weeks
Enjoyment questionnaire
Time frame: 4 weeks
Program feedback provided during a semi-structured interview at the end of the intervention.
University of Michigan
Other
Acronym: RT after APOs
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07342127
Factor II Heterozygous Mutation, Factor V Leiden Heterozygous Mutation
Bron, France
View Trial DetailsNCT06947837
Nurses, Postpartum
Wuhan, Hubei, China
View Trial DetailsNCT07089147
Coccydynia, Postpartum
Konya, Karatay, Turkey (Türkiye)
View Trial DetailsNCT07252466
Bonding, Newborn
Istanbul, Ataşehir, Turkey (Türkiye)
View Trial Details