Actively Recruiting
Physical Activity and Sedentary Behavior During Pregnancy
Led by University Hospital, Clermont-Ferrand · Updated on 2024-09-24
630
Participants Needed
1
Research Sites
159 weeks
Total Duration
On this page
Sponsors
U
University Hospital, Clermont-Ferrand
Lead Sponsor
R
Réseau de Santé en Périnatalité d'Auvergne
Collaborating Sponsor
AI-Summary
What this Trial Is About
Our main objective is to evaluate the intervention that best enables women's adherence to physical activity (PA). Our hypothesis is that identifying types of interventions suitable for pregnant women (in-person PA sessions, videoconferences or mixed format) could help improve their PA level and simultaneously reduce their sedentary behavior (SB).
CONDITIONS
Official Title
Physical Activity and Sedentary Behavior During Pregnancy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant women aged 18 years or older monitored for pregnancy in the Clermont-Ferrand metropolitan area
- Planning to give birth in a maternity unit in the Clermont-Ferrand metropolitan area (CHU Estaing or Clinique de la Chataigneraie)
- Agree to be randomized and follow the physical activity program offered
- Willing to participate in follow-up as part of the study
- Able to provide informed consent
- Affiliated with a social security scheme
- Between 14 weeks 0 days and 21 weeks 6 days of gestation
You will not qualify if you...
- Women under guardianship, curatorship, deprived of liberty, or under court protection
- History of recurrent miscarriage
- Multiple pregnancy
- Hemoglobin level below 9 g/dL or symptomatic anemia
- Eating disorders or body mass index (BMI) less than or equal to 18.5 or greater than or equal to 40
- Orthopedic limitations
- Cardiovascular or pulmonary disease
- Uncontrolled thyroid disease
- High level of smoking
- Significant health problems
- Premature rupture of membranes
- Premature labor during this pregnancy or history of at least 2 premature births
- Persistent vaginal bleeding
- Cervical incompetence
- Evidence of intrauterine growth restriction
- Uncontrolled epilepsy
- Diabetes (previous or gestational, diagnosed in the first trimester) or chronic hypertension
- Planned home birth
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CHU de Clermont-Ferrand
Clermont-Ferrand, France, 63000
Actively Recruiting
Research Team
L
Lise Laclautre
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
4
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