Viewing Study NCT06536595



Ignite Creation Date: 2024-10-26 @ 3:36 PM
Last Modification Date: 2024-10-26 @ 3:36 PM
Study NCT ID: NCT06536595
Status: COMPLETED
Last Update Posted: None
First Post: 2024-07-29

Brief Title: Validity and Reliability of the Turkish Version of HAnDE
Sponsor: None
Organization: None

Study Overview

Official Title: Validity and Reliability of the Turkish Version of the Hand Scleroderma Lived Experience Scale
Status: COMPLETED
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The aim of the present study was to translate and cross-culturally adapt The Hand Scleroderma Experienced Experience HAnDE Scale into the Turkish language and investigate its reliability and validity in Turkish-speaking patients with systemic sclerosis
Detailed Description: Objective The aim of the present study was to translate and cross-culturally adapt The Hand Scleroderma Experienced Experience HAnDE Scale into the Turkish language and investigate its reliability and validity in Turkish-speaking patients with systemic sclerosis

Methods The HAnDE was cross-culturally adapted according to Beatons guideline Participants completed the Turkish version of HAnDE scale HAnDE-T The Mouth Handicap in Systemic Sclerosis Scale MHISS 36 Item Short Form Survey SF-36 Health Assessment Questionnaire HAQ Internal consistency of the HAnDE-T questionnaire was evaluated by Cronbachs alpha coefficient Convergent validity was tested using Pearsons correlation coefficient The construct validity of the HAnDE-T questionnaire was assessed by factor analysis The construct validity of the HAnDE-T was evaluated by correlating the scores between HAnDE-T and HAQ SF-36 PCS SF-36 MCS and MHISS scores

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None