Clinical trial Recruiting at 1 site Interventional Women only

Impact of activity levels on preterm delivery risk in women with a short cervix

Official title: The Effect of Routine Activity on the Risk for Preterm Delivery in Women With a Short Cervix. A Randomized Control Trial

Run by Wolfson Medical Center · NCT06884761 · Data updated 2026-11-12

This study is testing if staying active instead of resting a lot can help pregnant women with a short cervix avoid having their babies too early.

Quick facts

Study typeInterventional
SexWomen only
Enrollment100 (estimated)
SponsorWolfson Medical Center
Government
Locations1 site (Holon)
StatusRecruiting
StartedJanuary 15, 2025
Main results expectedDecember 29, 2027
Study endsDecember 29, 2027
Registry record updatedApril 17, 2025
Trial IDNCT06884761 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are pregnant women with singleton pregnancies between 24 and 34 weeks who have a cervical length of less than 25 mm.

Probably not a fit

Patients with twin pregnancies, medical contraindications to physical activity, or other serious maternal or fetal complications may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial evaluates the effects of routine physical activity compared to strict bed rest on the risk of preterm delivery in pregnant women diagnosed with a short cervix between 24 and 34 weeks of gestation. Participants will be randomized into two groups: one group will maintain their usual activity levels while the other will be advised to rest maximally. The study aims to determine if routine activity influences gestational age at delivery and secondary outcomes such as preterm labor and maternal anxiety. Participants will wear a smart band to monitor their activity levels over a two-week period and will have regular follow-ups at a high-risk pregnancy clinic.

Why it matters

Potential benefit: If successful, this study could provide evidence that routine activity may reduce the risk of preterm delivery in women with a short cervix.

How similar studies have gone: While there have been studies on activity levels during pregnancy, this specific approach focusing on women with a short cervix is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
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.

Where it's running

  • The Edith Wolfson Medical Center
    Holon, Israel
    Recruiting

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.