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Physical Activity and Sedentary Behavior During Pregnancy

Study acronym: PREGMOUV
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 11 months later Oct 2027 → Oct 2028
See other at-risk trials from University Hospital, Clermont-Ferrand

Record History

See every version on ClinicalTrials.gov ↗

  1. Notable Primary and study completion pushed from Oct 2027 to Oct 2028 Show 5 more changesShow less
    • Primary endpoints: details revised at 1 of 1 entry
    • Enrollment target: 630 to 654
    • Eligibility criteria expanded, about 24 words
    • Secondary endpoints: details revised at 12 of 35 entries
    • Collaborators: details revised at 2 of 6 entries
  2. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Sep 2024 to Sep 10, 2024
    • Site details revised
    v2
  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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).
Trial Details
NCT Number NCT06585085
Lead Sponsor University Hospital, Clermont-Ferrand
Collaborators: Réseau de Santé en Périnatalité d'Auvergne, ASM Omnisports - Pôle Sport-Santé, Office Municipal du Sport - Espace Sport Santé, Observatoire national de l'activité physique et de la sédentarité, Ville de Clermont-Ferrand, Ministère de la Santé et de la Prévention
Conditions
(from sponsor)
Pregnant Woman
Related terms Motor Activity
Enrollment 654 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov