- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04423705
The Turkish Version of The Active-Q: Physical Activity Questionnaire
The Turkish Version of The Active-Q: Physical Activity Questionnaire: A Reliability and Validity Study
Study Overview
Status
Conditions
Detailed Description
Individuals forming modern societies along with technological developments are increasingly adopting sedentary lifestyle. This situation increases the risks in terms of morbidity and mortality. For this reason, especially all countries build their health policies on increasing physical activity and make strides to improve it. In order to reach the ideal physical activity level, the physical activity level should be evaluated. However, when the literature is evaluated, it is possible to come across different and many physical activity evaluation methods. This makes it difficult to compare. On the other hand, many researchers prefer to use scales and surveys because of their low costs and ease of use. Although there are many physical activity assessment scales in the literature based on age, gender, disorder or disease, social needs and other features, many of them cannot be used in our society because they are not Turkish. This poses an important obstacle for Turkish researchers to evaluate physical activity.
"The Active-Q: Physical Activity Questionnaire" is a web-based scale developed to investigate the absence of physical activity and activity for individuals over the age of 18. Individuals are asked to answer questions about their activity habits in the past year. By developing the scale, Bonn et al. Tested its validity and reliability comparatively with the 'Double labeled water' method and the accelerometer.
The investigators think that "The Active-Q: Physical Activity Questionnaire" will help physiotherapists and other health professionals in the field and in the field to evaluate individuals' physical activity by revealing their energy consumption values. Therefore, it was aimed to make this scale available to Turkish healthcare professionals by conducting the Turkish validity and reliability study.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- to be a native Turkish speaker
- to be a volunteer
Exclusion Criteria:
- to make any form of weight alternation diet
- to be pregnant
- to have given birth during last 1 year
- to have any chronic and/or orthopedic disease/problem/syndrome
- to have any traumatic injury or any form of surgery during last 1 year
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Reliability: The Active-Q
Time Frame: 2 months
|
To measure stability of the test over time by The Active-Q: Physical Activity Questionnaire.
The Active-Q is filled with one week interval.
|
2 months
|
Validity- IPAQ-SF
Time Frame: 2 months
|
To test in order to establish the correlation among the proposed instrument and instruments that had already been translated and validated.
The Short Form of the International Physical Activity Questionnaire (IPAQ-SF) is used.
|
2 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Elif Karagül, Mac, HACETTEPE UNIVERSİTY
- Principal Investigator: Sibel Bozgeyik, PhD, HACETTEPE UNIVERSİTY
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
- GO 19/776
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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