Actively Recruiting
Baylor Continence Scale in Children With Anorectal Malformations: A Turkish Validity and Reliability Study
Led by Izmir Bakircay University · Updated on 2026-02-17
230
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
Sponsors
I
Izmir Bakircay University
Lead Sponsor
E
Ege University
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the validity and reliability of the Baylor Continence Scale adapted for Turkish-speaking children diagnosed with anorectal malformations. This study aims to standardize continence assessment in Turkish clinical settings, helping healthcare providers make informed treatment and follow-up decisions for pediatric patients with this condition. The study focuses on children aged 6 to 18 years who have undergone surgery for anorectal malformations. The main intervention is the Turkish version of the Baylor Continence Scale, which will be tested for language adaptation, statistical validity, and reliability in this population. The study is observational and includes data collection over an average of 6 to 12 months to analyze the scale's performance. This approach may be among the first to validate this tool specifically for Turkish children with anorectal malformations. Participants and their caregivers will be involved in completing the scale and providing relevant information during the study period. Researchers will assess the scale's validity and reliability through statistical methods. The primary outcome is the validity and reliability analysis of the scale. The study does not involve treatment administration but focuses on assessment accuracy in children who have already undergone surgery. The study is scheduled to end in June 2026.
CONDITIONS
Brief Title
Baylor Continence Scale Validity in Anorectal Malformation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Having undergone surgery due to anorectal malformation
- Being between 6 and 18 years old
- The child and caregiver are required to know Turkish
You will not qualify if you...
- The child and caregiver having comprehension, hearing, or vision problems
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 6 to 12 months
Participants complete the Baylor Continence Scale to assess continence status after surgery for anorectal malformations.
Trial Site Locations
Total: 1 location
1
Ege University Department of Pediatric Surgery and Bakırçay University Physical Therapy and Rehabilitation Application and Research Center
Izmir, Turkey (Türkiye)
Actively Recruiting
Research Team
A
Ayşe Kayalı Vatansever, Assistant Professor, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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