便秘患者におけるWexner質問票の異文化適応、妥当性、信頼性
Wexner質問票の異文化間適応、妥当性、および信頼性
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.
調査の概要
詳細な説明
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.
研究の種類
入学 (実際)
連絡先と場所
研究場所
-
-
Centre
-
Kırşehir、Centre、トルコ（Türkiye）、40000
- Kirşehir Ahi Evran University Physical Therapy and Rehabilitation Hospital
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
サンプリング方法
調査対象母集団
Men and women with chronic constipation
説明
Inclusion Criteria:
- 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.
Exclusion Criteria:
- Not wanting to continue the study.
- Having any complaints, such as anorectal bleeding, during the test-retest interval.
研究計画
研究はどのように設計されていますか？
デザインの詳細
- 観測モデル：CASE_ONLY
- 時間の展望：PROSPECTIVE
この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Application of survey to participants
時間枠：Baseline (Day 1)
|
First administration of the Wexner questionnaire to all participants |
Baseline (Day 1)
|
|
Application of survey to participants
時間枠：Baseline (Day 1)
|
First administration of the quality of life questionnaire to all participants |
Baseline (Day 1)
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Application of survey to participants
時間枠：Baseline (Day 1)
|
Wexner questionnaire were administered to the participants a second time two weeks later. |
Baseline (Day 1)
|
|
Application of survey to participants
時間枠：Baseline (Day 1)
|
Quality of life questionnaire were administered to the participants a second time two weeks later. |
Baseline (Day 1)
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- KAEU-EBAYRAMOGLUD-003
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。