Menu
Recruiting NCT07029984

Baylor Continence Scale Validity in Anorectal Malformation

Observational Anorectal Malformations

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Baylor Continence Scale.
Who it may be relevant to
Registry conditions: Anorectal Malformations. Basic parameters: 6 years — 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Baylor Continence Scale in Children With Anorectal Malformations: A Turkish Validity and Reliability Study

Overview

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.

Interventions

  • Other Baylor Continence Scale
    This study may be one of the first to test the Turkish adaptation and validity of the scale in Turkish children with anorectal malformations.

Primary outcome measures

  • Validity and Reliability Analyses [Time frame: Average 6 to 12 month]

Eligibility criteria

Inclusion criteria

  • Having undergone surgery due to anorectal malformation
  • Being between 6 and 18 years old
  • The child and caregiver are required to know Turkish

Exclusion criteria

  • The child and caregiver having comprehension, hearing, or vision problems

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

Turkey (Türkiye) · 1 center
  • Ege University Department of Pediatric Surgery and Bakırçay University Physical Therapy an — Izmir

Identifiers

NCT: NCT07029984 · 2015

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗