- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03743454
Physical Activity Level and Physical Activity Awareness
Relationship Between Physical Activity Level And Physical Activity Awareness In Young Adults
It is important to determine the attitudes and behaviors of individuals towards regular exercise participation in order to direct individuals to physical activity or to implement effective practices related to increasing their participation.
The aim of this study was to determine the awareness of physical activity in young adults, the relationship between physical activity awareness and physical activity level and to investigate the differences between sexes.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Edirne, Turkey
- Nimet Sermenli Aydın
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- healthy young females and males who want to participate to the study
- individuals who have smartphones
Exclusion Criteria:
- have orthopedic, physiologic, psychiatric, neurologic or systemic disorders
- have present medication
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Women
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No intervention will be applied.
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Men
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No intervention will be applied.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Physical Activity Level
Time Frame: After the individuals permission, its taken in the first minute.
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Physical activity will be assessed with IPAQ-SF questionnaire.
IPAQ-SF is a self-report questionnaire that assesses PA in the last 7 days.
Using the IPAQ-SF scoring system, the total number of days and minutes of PA were calculated for each participant as recommended in the IPAQ website.
The IPAQ-SF records the activity in four intensity levels: sitting, walking, moderate intensity (e.g., leisure cycling), and vigorous intensity (e.g, running or aerobics).
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After the individuals permission, its taken in the first minute.
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Physical Activity Awareness
Time Frame: After they completed the IPAQ-SF, its taken in the sixth minute.
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Physical activity awareness will be assessed with Cognitive Behavioral Physical Activity Questionnaire (CBPAQ).
The CBPAQ scale consists of 15 items, including three sub-dimensions: personal barriers, outcome expectations and self-regulation.
The individual items are rated at 1-5 according to the situation in which they are most appropriate.
The higher the score, the higher the level of awareness.
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After they completed the IPAQ-SF, its taken in the sixth minute.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of Steps
Time Frame: After the individuals permission, number of steps will be taken at the end of the first week.
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Number of steps will be evaluated by smartphone pedometer.
Pedometer provides data about the number of steps taken by the individual, so it accurately measures the individual's walking activity only.
Individuals which has less than 5000 steps per day were classified as "sedentary", 5000-7499 steps "low active," 7500-9999 "somewhat active" and 10000 steps and more were classified as 'active'.
Number of steps per week will be taken from individuals and mean steps per day will be calculated from number of steps per week.
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After the individuals permission, number of steps will be taken at the end of the first week.
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- TUTF-BAEK 2018-159
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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