Adaptation and Validity of the Lithuanian Version of the Baecke Physical Activity Questionnaire

March 12, 2026 updated by: Ernesta Aukštuolytė

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

Enrolling by invitation

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

150

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Kaunas, Lithuania
        • Lithuanian University of Health Sciences

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Eligible participants will include women and men aged ≥18 years.

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 2, 2026

Primary Completion (Estimated)

February 2, 2029

Study Completion (Estimated)

February 2, 2029

Study Registration Dates

First Submitted

February 4, 2026

First Submitted That Met QC Criteria

February 4, 2026

First Posted (Actual)

February 11, 2026

Study Record Updates

Last Update Posted (Actual)

March 16, 2026

Last Update Submitted That Met QC Criteria

March 12, 2026

Last Verified

March 1, 2026

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)?

NO

IPD Plan Description

IPD will not be shared to protect participant privacy and confidentiality.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

Clinical Trials on Validation

Clinical Trials on No Interventions

Subscribe