🔎 Trials Near Me

Home › NCT05849649

Mobile Application-based Exercise Intervention for Pregnant Women

RecruitingHealthy volunteers welcome

Increasing Physical Activity Through a Mobile Health Intervention Among Pregnant and Postpartum Women in a Rural Setting

Who can join

Ages 18 to 44 · Women · Healthy volunteers welcome

Full eligibility criteria
Inclusion Criteria:

* Age 18-44
* Confirmed singleton viable pregnancy
* English-Speaking (the app is currently only available in English)
* Physician release to participate in exercise prior to study participation
* Ownership of a smartphone
* Patient at either Graves Gilbert Clinic or Women's Health Specialists
* Plans to deliver at The Medical Center in Bowling Green, KY.

Exclusion Criteria:

* Multiple gestation pregnancy
* Inability to provide voluntary informed consent
* Any medical condition (pregnancy-related or not) that would preclude exercise.

About the study

The overarching goal of this randomized controlled clinical trial is to test the efficacy of the mHealth app (BumptUp) for improving physical activity levels among pregnant and postpartum women in a rural setting. Secondary outcomes include weight status, dietary intake, glucose tolerance, blood pressure, and mental health.

Specific Aim 1. Conduct an RCT (N=176) to assess the efficacy of the mHealth intervention for increasing physical activity levels during pregnancy (13-15, 23-25, and 35-37 weeks gestation) and postpartum (6 and 12 weeks) among women in a rural setting.

Research Activities: The efficacy of BumptUp® will be determined by measuring physical activity levels (via accelerometry and surveys) between women who use the mobile app (intervention) and women who use only an educational brochure (attention control).

Specific Aim 2: Assess the efficacy of the mHealth intervention on important obstetric outcomes including maternal weight status, dietary intake, glucose tolerance, blood pressure, and mental health.

Research Activities: Maternal weight status, glucose tolerance, and blood pressure values will be obtained from patient charts. Dietary intake will be assessed via the National Cancer Institute Multifactor Screener. Maternal mental health status will be measured via The Edinberg Postpartum Depression Questionnaire, Center for Epidemiological Studies Depression Scale, and the State-Trait Anxiety Inventory.

What is being tested

Sponsor: Western Kentucky University · Participants: 176 · Started: Aug 1, 2023

Contact the study team

Official record on ClinicalTrials.gov — NCT05849649

Locations in the U.S.

KentuckyRachel Tinius, Bowling Green

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.