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Enrolling by Invitation

NCT Number: 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.

Enrolling by Invitation

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Key information

Conditions

Questionnaires Validation

Age range

18 month and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Lithuanian University of Health Sciences

Kaunas, Lithuania

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

No interventions

Other

No interventions

Primary outcomes

  1. 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.

Sponsors and collaborators

Lead sponsor

Ernesta Aukštuolytė

Other

Registry information

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Feb 11, 2026
Registry last updated
Mar 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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