NCT06234865

Technology-based Constipation Prevention Training

The Effect of Technology-based Constipation Prevention Training on Constipation Management in Hospitalised Orthopaedic Patients
Mehmet Akif Ersoy University·ClinicalTrials.gov·otherRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Constipation
Drug/Device/Intervention
Control Group
Study type
Interventional
Intervention type
other
Sponsor & location
Primary sponsor
Mehmet Akif Ersoy University
Location
Burdur, Turkey
Timeline & enrollment
Phase
N/A
Start date
Feb 08, 2024
End date
Nov 01, 2024
Enrollment
70 participants
Primary outcome

Bristol Stool Consistency Scale,Costipation Severity Scale

Summary

The aim of this study is to determine the effect of technology-assisted constipation
 prevention training on the management of constipation in hospitalised orthopaedic patients.
 This is a quasi-experimental study. The population of the study will consist of patients
 admitted to the Orthopaedic Clinic of Burdur State Hospital between January 2024 and November
 2024. The sample of the study is planned to consist of patients over 18 years of age, who are
 able to communicate, who do not have sensory loss related to advanced vision and hearing, who
 do not have psychiatric disorders at a level that prevents communication, and who are
 hospitalised at the Orthopaedic Clinic and who volunteer to participate in the research. Data
 for the study will be collected using the Patient Introduction Form, Constipation Risk
 Assessment Scale (CRAS), Bristol Stool Consistency Scale, Use of Constipation Prevention
 Methods Form, Constipation Education Questionnaire, Constipation Severity Scale. During
 the implementation of the research, it is planned to form two groups, the first 35 patients
 in the control group and the second 35 patients in the experimental group, from the patients
 hospitalised in the Orthopaedic Clinic. The data will be collected at 3 times: (1) before the
 training, (2) 2 weeks after the training, (3) 4 weeks after the training. The data will be
 digitalised in the SPSS 23 package and the necessary statistical analyses will be performed.

ICD-10 classifications
ConstipationIrritable bowel syndrome with predominant constipation [IBS-C]Other laxativesPoisoning: Other laxativesOther functional intestinal disorders
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06234865
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06234865 through Pure Global AI's free database. This phase not specified trial is sponsored by Mehmet Akif Ersoy University and is currently Recruiting. The study focuses on Constipation. Target enrollment is 70 participants.

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