The Effect of Bowel Preparation Training Given to Patients Undergoing Colonoscopy (training)

December 6, 2023 updated by: Saglik Bilimleri Universitesi

The Effect of Bowel Preparation Training Given to Patients Planned to Undergo Colonoscopy and the Monitoring Carried Out by the Nurse on Anxiety, Compliance With Bowel Preparation and Bowel Cleansing

This study was planned to examine the effect of bowel preparation training and monitoring given to patients planned to undergo colonoscopy on the level of anxiety, compliance with bowel preparation and bowel cleansing. The research sample was collected at the Sultan II. University of Health Sciences affiliated to the Istanbul Provincial Health Directorate between December 2022 and August 2023. 34 intervention and 34 control groups will be randomly selected from outpatients who apply to the Colonoscopy Unit of Abdülhamid Han Training and Research Hospital and meet the inclusion criteria.

In this study, it is aimed to increase the effect of bowel preparation training, supported by nurses in the clinic and via instant messaging/calling or communication application, on patients' anxiety level, level of compliance with bowel preparation, and bowel cleansing in patients scheduled for colonoscopy.

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

80

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
    • Uskudar
      • Istanbul, Uskudar, Turkey, 34100
        • University of Health science

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Colonoscopy is planned
  • Understands Turkish, can read and write,
  • Patients who volunteer to participate in the research.

Exclusion Criteria:

  • Patients who do not attend planned training and do not receive telephone counseling

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Control Group: Data Collection

  1. PRE-TEST

    a) Who is decided to have a colonoscopy, using the Patient Information Survey, Procedure Compliance Survey and Beck Anxiety Scale.

  2. ROUTINE APPLICATION

    1. Patients who are planned to undergo colonoscopy and are included in the control group will be trained according to the bowel preparation protocol routinely applied by the clinical nurse.
    2. The Procedure Compliance Survey, which is routinely used as a clinical procedure, is given to the patient/patient's relative after the training of the clinical nurse.

  3. FINAL TEST

    1. Immediately after the procedure, data will be collected again with the Patient Information Survey, Procedure Compliance Survey and Beck Anxiety Scale.
    2. After the procedure, the cleanliness of the intestines will be evaluated by the physician with the Ottawa Bowel Preparation Scale.
    3. The control group will be given training and a booklet after all data collection is completed.
Other: Intervention group: nurse-led education for bowel preparation of colonoscopy

  1. PRE-TEST

    a) Patients will be evaluated using the Patient Information Survey, Procedure Compliance Survey and Beck Anxiety Scale.

  2. INTERVENTION

    1. Patients will be given face-to-face training in the clinic training room of the unit.
    2. After face-to-face training is given, an educational brochure will be given to the patient.
    3. If the patient is constipated, the bowel preparation diet is requested to be started 5 days in advance. If the patient is not constipated, the bowel preparation diet is started 3 days in advance.
    4. After the intervention group is given bowel preparation training, reminders about colonoscopy will be made via instant messaging 3 to 5 days before the day of the colonoscopy.

  3. LAST TEST

    1. Data will be collected again using the Patient Information Survey, Procedure Compliance Survey and Beck Anxiety Scale.
    2. The cleanliness of the intestines will be evaluated by the physician using the Ottawa Bowel Preparation Scale.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Patient Information Survey
Time Frame: baseline, pre-intervention (pre-colonoscopy procedure)
It includes data about the personal characteristics
baseline, pre-intervention (pre-colonoscopy procedure)
Beck Anxiety Inventory
Time Frame: pre-intervention (pre colonoscopy procedure)
It measures the level of anxiety before colonoscopy prosedure
pre-intervention (pre colonoscopy procedure)
Procedure Compliance Survey
Time Frame: immediately post-intervention (post colonoscopy procedure)
It measures the level of compliance to interventions after colonoscopy prosedure
immediately post-intervention (post colonoscopy procedure)
Ottawa Bowel Preparation Scale
Time Frame: immediately post-intervention (post colonoscopy procedure)
It is used to assess a patient's bowel preparation for colonoscopy
immediately post-intervention (post colonoscopy procedure)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Saglik Bilimleri Universitesi

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 15, 2023

Primary Completion (Actual)

August 15, 2023

Study Completion (Estimated)

December 15, 2023

Study Registration Dates

First Submitted

November 8, 2023

First Submitted That Met QC Criteria

December 6, 2023

First Posted (Estimated)

December 7, 2023

Study Record Updates

Last Update Posted (Estimated)

December 7, 2023

Last Update Submitted That Met QC Criteria

December 6, 2023

Last Verified

December 1, 2022

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • BBUYUKKILIC

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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