Baylor Continence Scale Validity in Anorectal Malformation
ConditionAnorectal Malformations
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age6-18
SponsorIzmir Bakircay University
About this trial
The aim of this study is to evaluate the validity and reliability of the Baylor Continence Scale in Turkish-speaking children diagnosed with anorectal malformations. The scale is used to assess continence levels, helping healthcare providers make informed decisions regarding treatment and follow-up. The study includes a sample of children with confirmed anorectal malformations, and data collection consists of language adaptation, statistical validation, and reliability testing. Results will contribute to the standardization of continence assessment in Turkish clinical settings, ensuring accurate evaluations for pediatric patients.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Having undergone surgery due to anorectal malformation
Being between 6 and 18 years old
The child and caregiver are required to know Turkish
Disqualifiers
The child and caregiver having comprehension, hearing, or vision problems
Trial population
Inclusion criteria for the study include children who have undergone surgery due to anorectal malformation, are between 6 and 18 years old. Exclusion criteria consist of cases where the child and caregiver have comprehension, hearing, or vision problems that could affect communication or participation in the study.
Trial design
Design model
Other
Time perspective
Cross-sectional
Treatments tested in this trial
Baylor Continence Scale
Other interventionThis study may be one of the first to test the Turkish adaptation and validity of the scale in Turkish children with anorectal malformations.
Treatment groups
230 Participants
are divided into 1 treatment groupGroup A: Children with Anorectal Malformations1 intervention
Trial outcomes
Primary outcomes
1
Validity and Reliability Analyses
In this study, validity and reliability analyses will be conducted as part of the Turkish adaptation of the Baylor Continence Scale.
Time frame
Average 6 to 12 monthSponsors and contacts
Click on the lead sponsor to view all of their trials.
Izmir Bakircay University
Lead sponsor
Ege University
Collaborator
Source ClinicalTrials.gov