Actively Recruiting
Routine Activity and Preterm Delivery Risk in Women With a Short Cervix
Led by Wolfson Medical Center · Updated on 2025-04-17
100
Participants Needed
1
Research Sites
154 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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. Undergo regular follow-ups at a high-risk pregnancy clinic and have their data collected through hospital records and smart band tracking. This randomized controlled trial will assess gestational age at delivery as the primary outcome, along with secondary maternal and neonatal outcomes, providing insight into the role of physical activity in managing pregnancies complicated by a short cervix.
CONDITIONS
Official Title
Routine Activity and Preterm Delivery Risk in Women With a Short Cervix
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant with a single baby between 24+0 and 34+6 weeks gestation
- Short cervical length less than 25 mm confirmed by transvaginal ultrasound
- No medical reasons preventing physical activity
You will not qualify if you...
- Pregnant with twins or higher-order multiples
- Medical conditions requiring reduced mobility, such as symphysiolysis or fall risk
- Maternal health issues, fetal distress, vaginal bleeding, premature rupture of membranes, or need for immediate delivery
AI-Screening
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Trial Site Locations
Total: 1 location
1
The Edith Wolfson Medical Center
Holon, Israel, 5822012
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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