Effect of Preoperative Abdominal Effleurage on Postoperative Constipation

Ege University

Status: Begins enrollment this month

Conditions: Abdominal Surgery; Constipation; Postoperative Constipation

Treatments: Behavioral: Abdominal Superficial Effleurage Training

Study type: Interventional

Funder types: Other

Identifiers

NCT07344532

MOzkeskin7126

Details and patient eligibility

About

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.

Full 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.

Enrollment: 42 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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42 participants in 2 patient groups

Abdominal Superficial Effleurage Group

Experimental group

Description:

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.

Treatment:

Behavioral: Abdominal Superficial Effleurage Training

Control Group

No Intervention group

Description:

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