AzTrials
AzTrials

Physical ActivityNCT04890756

The Greek Version of Modified Baecke Questionnaire

An observational study of Physical Activity, run by University of Thessaly.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study was to translate and investigate the validity and reliability of the modified Baecke Physical Activity Questionnaire (mBQ) in the Greek adult population. Read more about this study

Who is it for?
Ages 18 to 59 yearsHealthy volunteers can take part
Conditions the study is for
Physical Activity
What is being tested?
observational
How many people
145 participants
Where
No sites listed yet
Study dates
1 Oct 2015to 25 Mar 2021
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 59 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: Healthy

Who may be able to join

  • age above 18
  • Greek native speakers
  • Greek inhabitants
  • sufficient cognitive functioning.

Who cannot join

  • poor health status,
  • diagnosed with cardiovascular diseases
  • cardiac pacemaker,
  • medication that prevents exercise activity
  • neurological disorders with effect on the lower body
  • musculoskeletal disorders or injuries on the lower body in the last 3 months
  • PAR-Q health risk assessment form

About this study

Official title: Validity and Reliability of the Greek Version of the Modified Baecke Questionnaire

The purpose of this study was to translate and investigate the validity and reliability of the modified Baecke Physical Activity Questionnaire (mBQ) in the Greek adult population.

Read the detailed description

The purpose of this study was to translate and investigate the validity and reliability of the modified Baecke Physical Activity Questionnaire (mBQ) in the Greek adult population. The cross-cultural adaptation of the mBQ was performed according to official guidelines.The reliability was determined by filling out the mBQ, two times, one week apart. For validation, the scores between the mBQ and the IPAQ were compared and the correlation between mBQ and VO2max and between mBQ and interview (METS) were assessed.

Being tested
observational
Keywords
validation, reliability, adaptation, questionnaire, Greek version, Baecke
Medical subject headings
Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • observationalOther

    The reliability was determined (n=100) by filling out the mBQ, two times, one week apart (test-retest).

    For validation (n=45), the scores between the modified Baecke Questionnaire and the International Physical Activity Questionnaire were compared and the correlation between the modified Baecke Questionnaire and VO2max(via Astrand-Rhyming Cycle Ergometer Test) and between mBQ and interview (via METS) were assessed.

Study groups in NCT04890756
Study groupRoleWhat they receive
Reliability Group100 Healthy Adults
Receives: Other: observational
Validity Group45 Healthy Adults
Receives: Other: observational

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Reliability

    The reliability was determined by filling out the modified Baecke Questionnaire, two times, one week apart (test-Retest).

    Tool: Modified Baecke Questionnaire (test-retest)

    Measured: one week apart

  2. Validity

    For validation, the scores between the modified Baecke Questionnaire and the International Physical Activity Questionnaire (IPAQ) were compared and the correlation between Modified Baecke Questionnaire and VO2max (via Astrand-Rhyming Cycle Ergometer Test) and between modified Baecke Questionnaire and interview (via METS) were assessed.

    Tools:

    1. International Physical Activity
    2. Astrand-Rhyming Cycle Ergometer Test Questionnaires (VO2max)
    3. Interview (METS)

    2)

    Measured: 1) IPAQ ( Time Frame: 30 min) 2) Astrand-Rhyming Cycle Ergometer Test (Time Frame: 20 min) 3) Interview (Time Frame: 45 min) 4)Modified Baecke Questionnaire (Time Frame: 30 min)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 May 2021
  2. Study start1 Oct 2015
  3. Primary completion20 Jul 2016
  4. Study completion25 Mar 2021

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
145 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04890756
Sponsor's protocol ID
cepr_lab
Status last verified
May 2021
First submitted
22 Apr 2021
Last updated
18 May 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: GDPR protected

Publications

  • Stefanouli V, Kapreli E, Anastasiadi E, Nakastsis A, Strimpakos N. Validity and reliability of the Greek version of modified Baecke questionnaire. Public Health. 2022 Feb;203:58-64. doi: 10.1016/j.puhe.2021.11.017. Epub 2022 Jan 13.

    PubMed 35032916

Questions about this trial

What is this clinical trial studying?

An observational study of Physical Activity, run by University of Thessaly.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 May 2021. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Reliability (time frame: one week apart). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04890756, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 May 2021.

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