Patient Education and Text Message Reminders in Colonoscopy

April 21, 2025 updated by: Arif Murat Alagöz, Amasya University

The Effect of Patient Education and Text Message Reminders on Bowel Preparation and Anxiety Level Before Colonoscopy

This study will be conducted to examine the effects of detailed education and text message reminders given to patients undergoing colonoscopy on bowel cleansing, vital signs and anxiety.

Study Overview

Detailed Description

İntroduction: The highest level of bowel preparation before the colonoscopy procedure is necessary for the successful completion of colonoscopy. Considering that the bowel preparation procedures required for colonoscopy are performed by patients, it is very important to inform patients about the content and duration of diet and bowel preparation practices. Today, with the widespread use of technology in our lives, technological education methods such as web-based trainings, text message reminders, telemedicine methods have started to be used in patient education methods as well as classical methods.

Purpose: This study will be conducted to examine the effects of detailed education and text message reminders given to patients undergoing colonoscopy on bowel cleansing, vital signs and anxiety.

Method: This study will be a randomized controlled trial. hospital. The sample of the study will include individuals who will undergo colonoscopy procedure in the endoscopy unit of a state hospital and who meet the inclusion criteria. Data will be collected using personal information form, beck anxiety scale, boston bowel readiness scale. In this study, in addition to the standard patient education protocol, the effectiveness of colonoscopy education with more intensive content and supported by visuals and diagrams will be evaluated in the education group. Individuals in the other group will receive text message reminders, which is one of the new methods that have started to be used in patient education with the technology that has become widespread today.

Conclusion: It is thought that more intensive and materialized trainings and text message reminders to patients compared to standard colonoscopy preparations will increase the level of bowel cleansing, improve vital signs and reduce anxiety.

Study Type

Interventional

Enrollment (Actual)

84

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

      • Amasya, Turkey
        • Amasya U

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:

Individuals who understand Turkish

Individuals who know how to use a phone and read text messages

Individuals over 18 years of age

Patients undergoing colonoscopy for the first time

Exclusion Criteria:

Patients with cognitive dysfunction

Patients with neuro-psychiatric disorders

Individuals who do not know how to use a phone

Individuals undergoing colonoscopy in emergency situations

Individuals who did not give consent to participate in the research

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: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Education Group
The training material will be created by researchers by reviewing national and international guidelines for colonoscopy practices. Using the "Colonoscopy Patient Preparation Guide", individuals will be given face-to-face, information and preparation training on colonoscopy preparation, its importance, the preparation medication to be used and the procedure process for an average of 15-20 minutes in a private room in the unit. After the training, individuals will be given the "Colonoscopy Patient Preparation Guide" brochure developed by the researchers.
The training material will be created by researchers by reviewing national and international guidelines for colonoscopy practices. Using the "Colonoscopy Patient Preparation Guide", individuals will be given face-to-face, information and preparation training on colonoscopy preparation, its importance, the preparation medication to be used and the procedure process for an average of 15-20 minutes in a private room in the unit.
Experimental: Text Message Group
Individuals will be subjected to the routine colonoscopy preparation procedure of the hospital by the investigator. Starting three days before the colonoscopy is performed, individuals will be informed via text messages about the foods and beverages that they can consume in their diet and those that are forbidden to consume until the morning of the colonoscopy, the amount of fluids they should consume daily, the use of medication, the use of soda and enema, appointment time reminders.
. Starting three days before the colonoscopy is performed, individuals will be informed via text messages about the foods and beverages that they can consume in their diet and those that are forbidden to consume until the morning of the colonoscopy, the amount of fluids they should consume daily, the use of medication, the use of soda and enema, appointment time reminders.
No Intervention: Control Group:
Individuals in the control group will be subjected to the standard procedure applied in the clinic. No additional education and educational brochures will be given to these patients and text message reminders will not be applied.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Beck Anxiety Scale
Time Frame: One day
Beck Depression Scale (BDS) was developed by Beck. The scale was created to include clinical symptoms seen in depression. The items of the BDS are organized based on clinical observations and data. The scale consists of 21 symptom categories. Each symptom category is addressed with scored sentences ranging from 0-3. The maximum score that can be obtained from the scale is 63. A high total score on the scale indicates a high level or severity of depression
One day
Boston Bowel Readiness Scale
Time Frame: One day

The scale has a four-point (0-3) scoring system applied separately for each of the three parts of the colon.

3- 0 (İnsuffıcıent) : Unprepared colon in which the mucosa cannot be evaluated due to uncleared solid fecal matter.

  1. (Bad) = Part of the mucosa is visible in the colon, but other parts are not visible due to contamination, residual fecal matter and/or opaque fluid.
  2. (Good) = Colon mucosa is well visualized but there is a small amount of impurities, small pieces of stool and/or opaque fluid.
  3. (Excellent) = The entire mucosa of the colon is well visible. No impurities, small pieces of pus or opaque fluid.
One day

Collaborators and Investigators

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

Investigators

  • Study Chair: Neşe Uysal, Amasya U

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)

August 28, 2023

Primary Completion (Actual)

January 6, 2025

Study Completion (Actual)

April 14, 2025

Study Registration Dates

First Submitted

October 3, 2023

First Submitted That Met QC Criteria

October 3, 2023

First Posted (Actual)

October 10, 2023

Study Record Updates

Last Update Posted (Actual)

April 24, 2025

Last Update Submitted That Met QC Criteria

April 21, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • AmasyaU-MA-292

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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