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Clinical Trials in Turkey / NCT07344532
Active, not recruiting Not applicable

Effect of Preoperative Abdominal Effleurage on Postoperative Constipation

NCT07344532 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-03-10
Last updated
2026-07-07

Condition(s) studied

ConstipationAbdominal SurgeryPostoperative Constipation

Investigational drug(s) / intervention(s)

Abdominal Superficial Effleurage Training

Abdominal Superficial Effleurage Training: Abdominal superficial effleurage is a gentle abdominal massage technique involving stroking movements from the right upper quadrant toward the left lower quadrant of the abdomen. Participants will be trained preoperatively to perform the technique, which will take approximately five minutes per session and will be performed one to three times daily postoperatively during pain-free periods.

Study 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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients scheduled to undergo abdominal surgery * Patients who are able to communicate verbally * Patients who agree to participate in the study and provide written informed consent Exclusion Criteria: * Patients with preoperative constipation * Patients with known gastrointestinal diseases affecting bowel motility * Patients who are unable to perform abdominal superficial effleurage * Patients with cognitive impairment or communication difficulties * Patients who refuse to participate in the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ege University Izmir Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07344532 on ClinicalTrials.gov ↗ ← All trials in Turkey