Actively Recruiting
Weight Loss and Physical Fitness Following Pregnancy in Active Duty Women
Led by Tripler Army Medical Center ยท Updated on 2025-09-17
74
Participants Needed
2
Research Sites
170 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Pregnancy and delivery are major stressors on the female body and contribute significantly to permanent weight gain and associated morbidity in women. This can profoundly affect the ability of active duty (AD) women to advance in their career. The first 12 weeks postpartum are the time period during which the most significant weight loss occurs and is critical in achieving a healthy weight in the first year postpartum. Many factors contribute to effective weight loss in this period among which the most critical are diet, exercise, and sleep. Breast feeding and depression may also affect weight changes postpartum. Research has shown diet to likely be the most crucial of these factors. The PADaWL study is designed as a randomized controlled trial to assess the effects of dietary intervention on weight and physical fitness versus routine postpartum care in the first year postpartum. Subjects will be primiparous AD women from any military service recruited in the obstetric clinic in the third trimester of pregnancy at Tripler Army Medical Center. Data will collected in an ambi-directional fashion with pre-pregnancy physical fitness data, demographic and pregnancy data collected at time of enrollment. Subjects will be randomized to receive intensive virtual sessions with a dietician vs routine postpartum care for the first 12 months postpartum. We will utilize a biometric device to monitor activity levels and sleep, web-based diaries to monitor breast feeding and diet, and validated questionnaires to evaluate depression as well as diet and sleep. Subjects will be monitored weekly for the first 12 weeks postpartum and will then be further evaluated at 6, 9 and 12 months postpartum. Primary outcome is weight at 12weeks postpartum and whether subjects have achieved military standards. Secondary outcome will be weight at 12 months postpartum and whether subject has achieved weight and fitness standards. The study intends to collect large amounts of data, and we intend to analyze which factors may be contributing to weight retention postpartum. This study should provide an accurate assessment of the effects of pregnancy on AD women. It should generate a clean and accurate dataset on which multiple follow-on studies can be performed and provide data for designing further intervention studies in postpartum women. The results of this study should also be able to assist in developing policy and guidance concerning AD women and pregnancy.
CONDITIONS
Official Title
Weight Loss and Physical Fitness Following Pregnancy in Active Duty Women
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Active duty from any military service branch
- Any military rank
- First pregnancy
- Singleton pregnancy
- Delivery planned between 36 and 41 weeks of pregnancy
- Non-obese with BMI less than 30 at first trimester appointment
- Any type of delivery planned (vaginal or cesarean)
- Live birth expected
- Documented standardized fitness evaluation before pregnancy
- Plan to remain on active duty at least 18 months after delivery
- Not planning another pregnancy within 18 months after delivery
- Planning to stay on Oahu for at least 12 months after delivery
You will not qualify if you...
- Obese with BMI over 30 at first trimester appointment
- Delivery before 36 weeks of pregnancy
- Severe maternal complications requiring hospital stay longer than 1 week after delivery
- Newborn admitted to NICU for more than 2 weeks
- Physical limitations preventing exercise or fitness testing
- Planning to take leave or separate from duty within 18 months after delivery
- No fitness test recorded in the year before pregnancy
- Previous pregnancy beyond 20 weeks gestation
- Planning another pregnancy within 18 months after delivery
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Tripler Army Medical Center
Honolulu, Hawaii, United States, 96859
Actively Recruiting
2
Desmond Doss Health Clinic
Schofield Barracks, Hawaii, United States, 96786
Actively Recruiting
Research Team
A
Alan P Gehrich, MD
CONTACT
C
Chothika Mekonnen, BS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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