Effect of Preoperative Abdominal Effleurage on Postoperative Constipation

NCT ID: NCT07344532

Last Updated: 2026-01-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

42 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-03-10

Study Completion Date

2026-09-10

Brief Summary

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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.

Detailed Description

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Postoperative constipation is a common complication following abdominal surgery and may negatively affect patient comfort, recovery, and quality of life. Non-pharmacological nursing interventions that support bowel motility are therefore of increasing interest in perioperative care. Abdominal superficial effleurage is a gentle massage technique applied to the abdominal surface and is thought to stimulate intestinal peristalsis and promote bowel function.

This prospective, randomized controlled study will be conducted with patients scheduled to undergo abdominal surgery. A total of 42 patients will be randomly assigned to either the intervention group (n=21) or the control group (n=21) using a computer-generated randomization method. Patients in the intervention group will receive preoperative training on abdominal superficial effleurage in addition to routine clinical care, while patients in the control group will receive routine clinical care only. To minimize interaction between groups, data from the control group will be collected prior to the intervention group.

Abdominal superficial effleurage will be taught during the preoperative period and performed by patients postoperatively. The technique involves gentle stroking movements starting from the right upper quadrant of the abdomen and progressing toward the left lower quadrant. Each session will last approximately five minutes and will be performed one to three times daily during periods when the patient is not experiencing pain. Postoperative constipation will be evaluated on the 10th postoperative day through a telephone interview using the Bristol Stool Form Scale. Study data will be analyzed using appropriate descriptive and inferential statistical methods.

Conditions

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Constipation Abdominal Surgery Postoperative Constipation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Participants will be randomly assigned to either an intervention group receiving preoperative abdominal superficial effleurage training in addition to routine care or a control group receiving routine care only.
Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Abdominal Superficial Effleurage Group

Participants in this group will receive preoperative training on abdominal superficial effleurage in addition to routine clinical care. Following surgery, patients will perform the effleurage technique for approximately five minutes, one to three times daily, during periods without pain.

Group Type EXPERIMENTAL

Abdominal Superficial Effleurage Training

Intervention Type BEHAVIORAL

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.

Control Group

Participants in the control group will receive routine clinical care only and will not receive abdominal superficial effleurage training during the study period.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ege University

OTHER

Sponsor Role lead

Responsible Party

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Mehmet Ozkeskin

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Mehmet Ozkeskin, PhD

Role: PRINCIPAL_INVESTIGATOR

Ege University

Central Contacts

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Mehmet Ozkeskin, Associate Professor

Role: CONTACT

+90 505 663 18 33

Other Identifiers

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MOzkeskin7126

Identifier Type: -

Identifier Source: org_study_id

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