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NCT06243055 Clinical Trial

Reliability and Validity of the Turkish Version of the Laval

Obesity Clinical Trial

Official title:
Reliability and Validity of the Turkish Version of the Laval Quality of Life Questionnaire for Obesity

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06243055
Other study ID # 6617-GOA
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 15, 2021
Est. completion date September 20, 2023

Study information
Verified date January 2024
Source Ege University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study is a Turkish validity and reliability study of the Laval questionnaire.

Description:

the study was planned as a student's master thesis. the whole study was carried out by us. all evaluations were completed. all analyses were completed. It is an observational study. It is a survey study.The study data were entered retrospectively. Research İzmir Bayraklı District Health Directorate No. 1 Healthy Life Centre (1 October 2021 - 15 November 2021) and Gaziemir Municipality (15 November 2021 - 15 March 2022) was conducted. Dokuz Eylül University Ethics Committee accepted the study on 22.12.2021 with the decision number 2021/38-08. People with Body Mass Index ≥ 30 kg/m2 and who met the inclusion/exclusion criteria were included in the study. In addition to the Laval Questionnaire, the SF-12 general health quality of life questionnaire and the Obese-Specific Quality of Life Scale were used. For the adaptation of the Turkish version of the questionnaire, first, language validity was ensured by back translation method.

Recruitment information / eligibility
Status Completed
Enrollment 235
Est. completion date September 20, 2023
Est. primary completion date March 22, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - volunteering, being literate - age = 18 and age = 75 - body mass index (BMI) = 30 kg/m2 - ability to follow instructions to fill out questionnaires. Exclusion Criteria: - affected by psychiatric illness

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• questionnare
laval questionnare
• questionnare
Obese-Specific Quality of Life
• questionnare
SF-12 Quality of Life scale

Locations
Country Name City State
Turkey Izmir Bayrakli District Health Directorate No. 1 Healthy Life Centre Bayrakli I?zmi?r
Turkey Gaziemir Municipality Izmir Gaziemir

Sponsors (1)
Lead Sponsor Collaborator
Ege University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary the Kaiser-Meyer-Olkin (KMO) test to check the suitability of the sample number for analysis 1 year
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