NCT07344532

Brief 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.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
42

participants targeted

Target at P25-P50 for not_applicable

Timeline
4mo left

Started Mar 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress32%
Mar 2026Sep 2026

First Submitted

Initial submission to the registry

January 7, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

January 15, 2026

Completed
2 months until next milestone

Study Start

First participant enrolled

March 10, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 10, 2026

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 10, 2026

Last Updated

January 27, 2026

Status Verified

January 1, 2026

Enrollment Period

4 months

First QC Date

January 7, 2026

Last Update Submit

January 25, 2026

Conditions

Keywords

Postoperative ConstipationAbdominal SurgeryAbdominal EffleurageNon-Pharmacological Intervention

Outcome Measures

Primary Outcomes (1)

  • Postoperative Constipation

    Postoperative constipation will be assessed using the Bristol Stool Form Scale through a telephone interview conducted on the 10th postoperative day. Stool types 1 and 2 will be considered indicative of constipation.

    10 days postoperatively

Secondary Outcomes (1)

  • Stool Consistency

    10 days postoperatively

Study Arms (2)

Abdominal Superficial Effleurage Group

EXPERIMENTAL

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.

Behavioral: Abdominal Superficial Effleurage Training

Control Group

NO INTERVENTION

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

Interventions

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.

Abdominal Superficial Effleurage Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Constipation

Condition Hierarchy (Ancestors)

Signs and Symptoms, DigestiveSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Mehmet Ozkeskin, PhD

    Ege University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Mehmet Ozkeskin, Associate Professor

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: 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.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

January 7, 2026

First Posted

January 15, 2026

Study Start

March 10, 2026

Primary Completion (Estimated)

July 10, 2026

Study Completion (Estimated)

September 10, 2026

Last Updated

January 27, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share