- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04925115
Effect of Physical Activity on Academic Stress While Controlling the Confounding Variables
Study Overview
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Islamabad, Pakistan, 44000
- Recruiting
- Riphah International University
-
Contact:
- salman khan, MS-SPT
- Phone Number: 03329365147
- Email: salman_khan201390@yahoo.com
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Sub-Investigator:
- Waqar Ahmed Awan, PhD
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Principal Investigator:
- Salman Khan, MSPT-SPT
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Participants falling in this category would be recruited into the study.
- Moderate academic stress
Exclusion Criteria:
- Participant falling in this category would be excluded from the study.
- Physical Disability
- Acute infection
- Chronic infection
- Acute inflammation
- Chronic inflammation
- Known osteoporosis
- Individual with respiratory diseases e.g. asthma
- Smoking
- Musculoskeletal injuries
Confounding variables:
- Age
- Gender
- BMI
- Socio-economic status
- Semester
- Depression, anxiety and stress
- Demographic (rural, urban)
- Relationship status (married and unmarried)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Interventional group
Interventional group:
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Other Names:
|
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No Intervention: Control group
Routine activity of daily life
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Academic Stress scale
Time Frame: 6 weeks
|
Academic Stress will be measured through 40 item scale (Academic Stress scale).
It will be used during survey for inclusion criteria, This scale consists of 40 items describing the stress in your institution/ college life from the various sources.
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6 weeks
|
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Perceived stress scale
Time Frame: 6 weeks
|
Perceived stress scale will be measured through 10 questions in this scale ask you about your feelings and thoughts during the last month.
In each case, you will be asked to indicate by circling how often you felt or thought a certain way.
As 0 = Never 1 = Almost Never 2 = Sometimes 3 = Fairly Often 4 = Very Often
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6 weeks
|
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Depression, Anxiety and Stress Scale (DASS21)
Time Frame: 6 weeks
|
Depression, anxiety and stress scale will be measured through 21 items scale.
Moderate stress score is : 19-25
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6 weeks
|
|
Physical Activity Readiness Questionnaire (PAR-Q)
Time Frame: 6 weeks
|
Physical Activity Readiness Questionnaire (PAR-Q) Yes to one or more questions: If you have not recently done so, consult with your doctor by telephone or in person before increasing your physical activity and/or taking a fitness appraisal. Tell your doctor what questions you answered 'yes' to on PAR-Q or present your PAR-Q copy. After medical evaluation, seek advice from your doctor as to your suitability for: Unrestricted physical activity starting off easily and progressing gradually, and Restricted or supervised activity to meet your specific needs, at least on an initial basis. If you answered PAR-Q accurately, you have reasonable assurance of your present suitability for: A graduated exercise programme A fitness appraisal |
6 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
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
- REC/00930 Salman khan
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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