Effect of Preoperative Abdominal Effleurage on Postoperative Constipation

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorEge University

About this trial

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 criteria

Qualifiers

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

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Abdominal Superficial Effleurage Training

Treatment groups

42 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators