Reliability and Validity of the Turkish Version of the Laval
NCT ID: NCT06243055
Last Updated: 2024-02-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
235 participants
OBSERVATIONAL
2021-11-15
2023-09-20
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Validity and Reliability Study of Turkish Version of Body Perception Questionnaire
NCT04411394
THE EFFICIENCY OF TECHNOLOGY-BASED MOTIVATION EDUCATION ON OBESITY UNIVERSITY STUDENTS' WEIGHT MANAGEMENT.
NCT05301166
Turkish Validity and Reliability of Physiotherapist Self-Efficacy Questionnaire
NCT05335291
Effect of a Mobile App for Obese Children on Eating Attitudes, Eating Awareness, and Healthy Eating Self-Efficacy
NCT07289425
Evaluation of Quality of Life in Women
NCT04164628
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
ECOLOGIC_OR_COMMUNITY
RETROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
questionnare
laval questionnare
questionnare
Obese-Specific Quality of Life
questionnare
SF-12 Quality of Life scale
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* age ≥ 18 and age ≤ 75
* body mass index (BMI) ≥ 30 kg/m2
* ability to follow instructions to fill out questionnaires.
Exclusion Criteria
18 Years
75 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ege University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
AYŞE KAYALI VATANSEVER
İzmir Bayraklı District Health Directorate
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Gaziemir Municipality
Izmir, Gaziemir, Turkey (Türkiye)
İzmir Bayraklı District Health Directorate No. 1 Healthy Life Centre
Bayraklı, İ̇zmi̇r, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
6617-GOA
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.