The Effect of Reflexology on Time to Delivery During Induction of Labor
Recruiting · NCT07168187 · Interventional (participants receive a specific treatment) · Lead sponsor: Wolfson Medical Center
View the official record on ClinicalTrials.gov →Interventions studied
What this trial is about
This prospective, randomized controlled trial evaluates the effect of reflexology on maternal anxiety, labor duration, and pain in women undergoing labor induction with an extra-amniotic balloon (EAB). Eligible participants are women with a singleton, term pregnancy, cephalic presentation, intact membranes, and a Bishop score \<6, without prior cesarean delivery or contraindications to vaginal delivery. Participants will be randomized to two groups: an intervention group receiving reflexology by a certified practitioner following EAB placement, and a control group receiving standard care. Maternal anxiety will be assessed using the State-Trait Anxiety Inventory (STAI) before and after the intervention. Labor duration and pain scores will also be recorded. The study plans to enroll 84 participants over two years. Reflexology is a safe, non-invasive complementary therapy, and this study aims to determine whether it provides measurable benefits during labor induction.
Who can take part
Inclusion criteria
- Age of ≥18 years
- Gestational age of \>37 weeks
- Vertex presentation
- Intact membranes
- Station of the fetus's head \< S-4
- Bishop score of \<6.
Exclusion criteria
- Patients who had undergone a previous cesarean delivery
- Patients with a contraindication for vaginal delivery
- Patients with a known fetal malformation patients undergoing termination of pregnancy.
Where it is running
1 location listed.
- Edith Wolfson Medical Center - Holon, Israel