- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07402889
Adaptation and Validity of the Lithuanian Version of the Baecke Physical Activity Questionnaire
The aim of this study is to adapt the Baecke Questionnaire of Habitual Physical Activity for use in Lithuania.
Individuals who meet the following criteria may participate in this study:
Adults aged 18 years or older. Native Lithuanian speakers. Willingness to participate in the study by signing an informed consent form.
If a participant agrees to take part in this study, two visits to the Department of Sports Medicine at the Lithuanian University of Health Sciences (Eivenių St. 2, Kaunas) will be required. During the first visit, participants will complete the Baecke Questionnaire of Habitual Physical Activity and the International Physical Activity Questionnaire. Height and weight measurements will be taken, and participants will be asked to remove shoes and outer clothing. After one week, a follow-up visit will be scheduled, during which the Baecke Questionnaire of Habitual Physical Activity will be completed again.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
-
Kaunas, Lithuania
- Lithuanian University of Health Sciences
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adults aged 18 years or older.
- Native Lithuanian speakers.
- Willingness to participate in the study by signing an informed consent form.
Exclusion Criteria:
- none
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Single Group - Questionnaire Completion
|
No interventions
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Baecke Questionnaire of Habitual Physical Activity - test-retest reliability
Time Frame: 1 week between baseline and follow-up administration
|
The primary outcome is the consistency of responses to the Baecke Questionnaire of Habitual Physical Activity when completed by the same participants one week apart, to assess the reliability of the adapted Lithuanian version.
|
1 week between baseline and follow-up administration
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Baecke JA, Burema J, Frijters JE. A short questionnaire for the measurement of habitual physical activity in epidemiological studies. Am J Clin Nutr. 1982;36(5):936-942. doi:10.1093/ajcn/36.5.936
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- BE-2-143
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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