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Effect of Abdominal Massage on Bowel Evacuation After Cranial Surgery

Primary Purpose

Constipation, Abdominal Massage

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
abdominal massage
Sponsored by
Mersin University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Constipation focused on measuring Cranial surgery, bowel evacuation, constipation, abdominal massage, nursing

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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,

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    abdominal massage group

    control group

    Arm Description

    the abdominal massage group received a total of 30 minutes of massage, 15 minutes every morning and evening, until the first defecation.

    Routine care for the control group

    Outcomes

    Primary Outcome Measures

    Primery outcome: bowel sounds
    time return of bowel sounds
    Primery outcome: first defecation
    time of the first defecation

    Secondary Outcome Measures

    constipation risk
    constipation risk in intensive care unit

    Full Information

    First Posted
    April 27, 2020
    Last Updated
    April 30, 2020
    Sponsor
    Mersin University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04373772
    Brief Title
    Effect of Abdominal Massage on Bowel Evacuation After Cranial Surgery
    Official Title
    The Effect of Abdominal Massage on Bowel Evacuation After Cranial Surgery: A Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2020
    Overall Recruitment Status
    Completed
    Study Start Date
    July 1, 2015 (Actual)
    Primary Completion Date
    February 28, 2016 (Actual)
    Study Completion Date
    February 28, 2016 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Mersin University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    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.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Constipation, Abdominal Massage
    Keywords
    Cranial surgery, bowel evacuation, constipation, abdominal massage, nursing

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    prospective, parallel, two arm (1:1), randomized controlled clinical trial
    Masking
    Participant
    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.
    Allocation
    Randomized
    Enrollment
    80 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    abdominal massage group
    Arm Type
    Experimental
    Arm Description
    the abdominal massage group received a total of 30 minutes of massage, 15 minutes every morning and evening, until the first defecation.
    Arm Title
    control group
    Arm Type
    No Intervention
    Arm Description
    Routine care for the control group
    Intervention Type
    Other
    Intervention Name(s)
    abdominal massage
    Intervention Description
    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.
    Primary Outcome Measure Information:
    Title
    Primery outcome: bowel sounds
    Description
    time return of bowel sounds
    Time Frame
    up to 10 days
    Title
    Primery outcome: first defecation
    Description
    time of the first defecation
    Time Frame
    up to 10 days
    Secondary Outcome Measure Information:
    Title
    constipation risk
    Description
    constipation risk in intensive care unit
    Time Frame
    up to 24 hours

    10. Eligibility

    Sex
    All
    Gender Based
    Yes
    Gender Eligibility Description
    ≥18 years old
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    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,

    12. IPD Sharing Statement

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    Effect of Abdominal Massage on Bowel Evacuation After Cranial Surgery

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