Clinical Trial

Effect of Preoperative Abdominal Effleurage on Postoperative Constipation

Active, Not Recruiting
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Summary
This randomized controlled study aims to evaluate the effect of preoperative abdominal superficial effleurage training on the development of postoperative constipation in patients undergoing abdominal surgery. Participants will be randomly assigned to an intervention group receiving abdominal superficial effleurage training in addition to routine care or to a control group receiving routine care only. The effleurage technique will be taught preoperatively and performed by patients postoperatively. Postoperative constipation will be assessed on the 10th postoperative day using the Bristol Stool Form Scale. The findings of this study are expected to contribute to non-pharmacological nursing interventions for the prevention of postoperative constipation.
Protocol Amendment History 3 changes
critical Trial status changed: Not Yet Recruiting → Active, Not Recruiting 2026-07-08
notable Primary completion moved earlier: 2026-07-10 -> 2026-05-10 2026-07-08
minor Completion moved earlier: 2026-09-10 -> 2026-07-10 2026-07-08
Trial Details
NCT Number NCT07344532
Lead Sponsor Ege University
Conditions Constipation, Abdominal Surgery, Postoperative Constipation
Enrollment 42 participants
Start Date 2026-03-10
Primary Completion 2026-05-10 (estimated)
Study Completion 2026-07-10 (estimated)
Updated on ClinicalTrials.gov 2026-07-07