- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03586349
Cultural Adaptation of Sedentary Behavior Questionnaire and Reliability, Validity Research of Turkish Version
January 15, 2019 updated by: Begum Kara Kaya
The aim of this study is to adapt the Sedentary Behavior Questionnaire (SBQ) into the culture of Turkish and to work on the reliability and validity of it in healthy individuals between the ages of 18-64.
The permission was obtained via mail from Dori Rosenberg, who is the developer of the questionnaire, for its Turkish adaptation.
SPSS package programme will be used in the analysis,
Study Overview
Status
Completed
Conditions
Detailed Description
The aim of this study is to adapt the Sedentary Behavior Questionnaire (SBQ) into the culture of Turkish and to work on the reliability and validity of it in healthy individuals between the ages of 18-64.
Original form has nine questions but Spanish version of it had eleven questions so the investigators will translate Spanish version of SBQ.
At first step by using a forward-backward translation method, a translation and adaptation process will be performed.
At second step the validation process will be performed in a total of 200 healthy subjects aged between 18-64 years.
Subjects will fill sociodemographic information form, International Physical Activity Questionnaire Short Form, and SBQ Turkish version ( at baseline and after seven days).
Cronbach's alpha values, confirmatory factor analysis (CFA) will be evaluated for the reliability, construct and convergent validity.
Study Type
Observational
Enrollment (Actual)
210
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
-
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Istanbul, Turkey
- Biruni University
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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
18 years to 64 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Healthy adults aged between 18-64 years.
Description
Inclusion Criteria:
- Being a healthy individual between the ages of 18-64.
- No problem of reading, writing or understanding Turkish.
Exclusion Criteria:
- Severe trauma in the last 6 months.
- Having orthopedic, neurological, cardiovascular problems that restricts ambulation.
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
- Observational Models: Other
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Sedentary Behavior Questionnaire
Time Frame: 1 week
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Sedentary Behavior Questionnaire scales the amount of time spent doing 11 sedentary behaviors.Response options are none, 15 minutes or less, 30 minutes, 1 hour, 2 hours,3 hours, 4 hours, 5 hours, 6 hours or more.
In the scoring the time spent on each behavior is converted into hours (eg, a response of 15 minutes is recoded as .25 hours).
For the total scores of sedentary behavior, responsed hours per day for each behavior are summed separately for weekday and weekend days.
For the summary scores of total hours/day spent in sedentary behaviors (weekday and weekend) and total sedentary hours/week, responses higher than 24 hours/day are truncated to 24 hours/day.
There are not any normative variables of Sedentary Behavior Questionnaire.
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1 week
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
International Physical Activity Questionnaire Short Form
Time Frame: Day 1
|
International Physical Activity Questionnaire Short Form(IPAQ-SF) scales the types of intensity of physical activity and sitting time that people do as part of their daily lives.
The short form records the physical activity of 3 different intensity levels: 1) vigorous-intensity activity such as aerobics (8.0 MET), 2) moderate-intensity activity such as leisure cycling (4.0 MET), 3) walking (3.3 MET).
The IPAQ-SF questions activities for last 7 days with 7 items.
In the scoring total estimate physical activity in MET-min/week and time spent while sitting are calculated ( Ex. 4.0 METx activity dayx activity duration (in minutes) equals moderate-intensity activity total MET score).According to scores subjects are categorized as inactive (achieving <600 MET-min/week), minimally active (achieving a minimum of at least 600 MET-min/week and <3000 MET-min/week), active (>3000 MET-min/week).
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Day 1
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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)
January 1, 2018
Primary Completion (Actual)
July 1, 2018
Study Completion (Actual)
September 30, 2018
Study Registration Dates
First Submitted
July 2, 2018
First Submitted That Met QC Criteria
July 12, 2018
First Posted (Actual)
July 13, 2018
Study Record Updates
Last Update Posted (Actual)
January 16, 2019
Last Update Submitted That Met QC Criteria
January 15, 2019
Last Verified
July 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- STUDY
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.
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