- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06073782
Patient Education and Text Message Reminders in Colonoscopy
The Effect of Patient Education and Text Message Reminders on Bowel Preparation and Anxiety Level Before Colonoscopy
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Amasya, Turkey
- Amasya U
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
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
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.
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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.
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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.
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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
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One day
|
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Boston Bowel Readiness Scale
Time Frame: One day
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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.
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One day
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Neşe Uysal, Amasya U
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- AmasyaU-MA-292
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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