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Effect of Abdominal Massage on Bowel Evacuation After Cranial Surgery

The Effect of Abdominal Massage on Bowel Evacuation After Cranial Surgery: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04373772
Enrollment
80
Registered
2020-05-04
Start date
2015-07-01
Completion date
2016-02-28
Last updated
2020-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abdominal Massage, Constipation

Keywords

Cranial surgery, bowel evacuation, constipation, abdominal massage, nursing

Brief summary

Many factors in patients undergoing cranial surgery (CS) may affect the bowel evacuation of patients, resulting in constipation, which could lead to the use of the valsalva maneuver. The aim of this study was to determine the effect of abdominal massage (AM) on bowel evacuation of patients treated in intensive care units (ICU) after CS.

Detailed description

The sample of this prospective parallel two-arm randomized controlled trial included 80 patients who underwent CS. The patients were randomly assigned (1:1) to the AM and control groups. The constipation risk of all the patients following CS was assessed with Constipation Risk Assessment Scale (CRAS). Those patients in the AM group received a total of 30 minutes of massage, 15 minutes every morning and evening, until the first defecation. The bowel sounds of all the patients in the AM and control groups were assessed on a daily basis. The days when bowel sounds were heard and the first defecation took place were recorded in a Bowel Evacuation Form.

Interventions

OTHERabdominal massage

the patients in the AM group were given a total of 30 minutes of AM by the nurses (HD, OM) everyday for 15 minutes in the morning and evening.In this study AM, which included effleurage, strokes, petrissage and vibration techniques, was applied to the patients for 15 minutes in each session at 9:00 am and 9:00 pm.

Sponsors

Mersin University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Masking description

In this study, due to the nature of the intervention, only the patient was blinded. The researchers involved in the running of the study were not blinded.

Intervention model description

prospective, parallel, two arm (1:1), randomized controlled clinical trial

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients who * volunteered to participate in the study, * were 18 years old or older and underwent CS, * stayed in the ICU for ≥ 3 days,

Exclusion criteria

Patients who * have percutaneous endoscopic gastrostomy, * abdominal hernia, * irritable bowel syndrome * bowel cancer, * history of abdominal surgery, * pregnancy,

Design outcomes

Primary

MeasureTime frameDescription
Primery outcome: bowel soundsup to 10 daystime return of bowel sounds
Primery outcome: first defecationup to 10 daystime of the first defecation

Secondary

MeasureTime frameDescription
constipation riskup to 24 hoursconstipation risk in intensive care unit

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026