Ignite Creation Date:
2026-03-26 @ 3:17 PM
Ignite Modification Date:
2026-03-31 @ 11:10 AM
Study NCT ID:
NCT07344532
Status:
NOT_YET_RECRUITING
Last Update Posted:
2026-01-27
First Post:
2026-01-07
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Effect of Preoperative Abdominal Effleurage on Postoperative Constipation
Sponsor:
Ege University
Organization:
Study Overview
Official Title:
The Effect of Preoperative Abdominal Superficial Effleurage Training on the Development of Postoperative Constipation in Patients Undergoing Abdominal Surgery
Status:
NOT_YET_RECRUITING
Status Verified Date:
2026-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
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.
Detailed Description:
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.
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.
Study Oversight
Has Oversight DMC:
False
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?: