Effect of Preoperative Abdominal Effleurage on Postoperative Constipation
The Effect of Preoperative Abdominal Superficial Effleurage Training on the Development of Postoperative Constipation in Patients Undergoing Abdominal Surgery
1 other identifier
interventional
42
0 countries
N/A
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2026
Shorter than P25 for not_applicable
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
First Submitted
Initial submission to the registry
January 7, 2026
CompletedFirst Posted
Study publicly available on registry
January 15, 2026
CompletedStudy Start
First participant enrolled
March 10, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 10, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 10, 2026
January 27, 2026
January 1, 2026
4 months
January 7, 2026
January 25, 2026
Conditions
Keywords
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
EXPERIMENTALParticipants 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.
Control Group
NO INTERVENTIONParticipants 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.
Eligibility Criteria
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
- Ege Universitylead
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mehmet Ozkeskin, PhD
Ege University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- 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