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Routine Activity and Preterm Delivery Risk in Women With a Short Cervix

RecruitingNAAges any - anyFemaleWolfson Medical Center
NCT06884761 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The goal of this clinical trial is to evaluate the effect of routine activity versus rest on the risk of preterm delivery in pregnant women with a short cervix diagnosed between 24 and 34 weeks of gestation. The main questions it aims to answer are: Does routine activity influence the gestational age at delivery? How does routine activity affect secondary outcomes such as preterm labor, premature rupture of membranes, delivery mode, maternal anxiety, and satisfaction? Researchers will compare women instructed to maintain routine activity (control group) to women advised to practice maximal rest (intervention group) to see if physical activity impacts preterm birth outcomes. Participants will: Wear a smart band to monitor step counts over a two-week period. Be randomized into two groups: one encouraged to maintain routine activity and the other advised to follow strict rest protocols.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Singleton pregnancies between 24+0 and 34+6 weeks. * Short cervical length (\<25 mm) confirmed via transvaginal ultrasound. * No medical contraindications to physical activity. Exclusion Criteria: * Twin pregnancies or higher-order multiples. * Medical indications for reduced mobility (e.g., symphysiolysis, fall risk). * Maternal comorbidities, fetal distress, vaginal bleeding, PPROM, or need for immediate delivery.
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What it tests

  • Maximal Rest
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Where

1 site
The Edith Wolfson Medical Center
Holon, Israel
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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