跳至主要内容
临床试验/NCT07340203
NCT07340203已完成不适用

Cross-Cultural Adaptation, Validity, and Reliability of the Wexner Questionnaire

Ahi Evran University Education and Research Hospital1 个研究点 分布在 1 个国家目标入组 202 人开始时间: 2025年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
202
试验地点
1
主要终点
Application of survey to participants

研究概览

简要总结

The investigators will conduct a validity and reliability study of the Wexner Constipation Questionnaire, used for constipation, in Turkish. For this purpose, investigators will administer the Wexner Questionnaire, translated from English to Turkish, and the accompanying Constipation Quality of Life Scale to 200 participants. Investigators will repeat the Wexner questionnaire for some participants after two weeks.

详细描述

To assess the cultural adaptation, validity, and reliability of the eight-question Wexner Constipation Questionnaire, the questionnaire was first translated from English to Turkish, then back from Turkish to English, and finally back from English to Turkish. The questionnaire was finalized with the collaboration of an internal medicine specialist and a gastroenterologist to prepare the Turkish version. It will then be administered to a minimum of 200 participants, along with the Constipation Quality of Life Questionnaire, previously validated and reliable in Turkish and used for constipation. For reliability, the questionnaire will be repeated for a portion of the participants after two weeks.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Being over 18 years of age
  • •Being diagnosed with functional constipation according to Rome IV criteria
  • •Having undergone an anorectal examination by a gastroenterologist
  • •Having no history of neurodegenerative disease (e.g., multiple sclerosis, spinal cord injury, or stroke)
  • •Having no history of metabolic disorders (e.g., diabetes, hypothyroidism, or hypercalcemia)
  • •Having no history of opioid-induced constipation
  • •Having no history of irritable bowel syndrome
  • •Having no history of congenital anorectal abnormality
  • •Having no history of colon cancer or pregnancy
  • •Having the ability to read and write Turkish.

排除标准

  • •Not wanting to continue the study.
  • •Having any complaints, such as anorectal bleeding, during the test-retest interval.

结局指标

主要结局

Application of survey to participants

时间窗: Baseline (Day 1)

First administration of the Wexner questionnaire to all participants

Application of survey to participants

时间窗: approximately 1 month

First administration of the Wexner questionnaire to all participants

次要结局

  • Application of survey to participants(Baseline (Day 1))
  • Application of survey to participants(approximately 1 week)

研究者

发起方
Ahi Evran University Education and Research Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Esra BAYRAMOĞLU DEMİRDÖĞEN

Lecturer Doctor

Ahi Evran University Education and Research Hospital

研究点 (1)

Loading locations...

相似试验