- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04221022
PHYSICAL ACTIVITY AS COPING STRATEGY FOR ACADEMIC STRESS AMONG UNDERGRADUATE FEMALE COLLEGIATE STUDENT
June 29, 2020 updated by: Zohra Institute of Health Sciences
Physical Inactivity is one of the major cause causing academic stress in students, so effectiveness of Light, moderate and vigorous physical activity as a baseline treatment were assessed through academic stress scale questionnaire, Cohen Perceived stress Scale and rapid assessment of physical activity (RAPA).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
A total of 388 students participated in first phase of study and total 60 students with moderate academic stress were filtered.
Among those only 37 were physically inactive from last one month by the assessment through RAPA (Rapid assessment of physical activity).
ASS (Academic stress scale), Cohen Perceived stress Scale and RAPA questionnaires were used to collect data.
Three equally distributed groups were given three different modes of physical activities i.e light, moderate & vigorous.
Study Type
Interventional
Enrollment (Actual)
37
Phase
- Not Applicable
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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KP
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Peshawar, KP, Pakistan, 25000
- Syed Alamdar Hussain
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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
16 years to 22 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Undergraduate female students between 18-24 years.
- Students with moderate level of academic stress
- Students inactive from last one month
Exclusion Criteria:
- Students with any other type of stress
- Students with other psychological disorders
- Student with known systemic disease.
- Physically active from last one month were excluded.
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
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Light physical activity (Group 1)
Female collegiate students were assessed by using Academic stress scale questionnaire, Cohen Perceived stress Scale and rapid assessment of physical activity (RAPA) to determine physical activity level and academic stress.
They were assigned into Light Physical activity.
Each subject in first group completed 6 weeks of exercise sessions which aimed to cope up academic stress among female collegiate students.
Each subject was evaluated for changes in symptoms in each week.
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Each session started with leisure walk, duration of which was set to 35 minutes.
Frequency set for the session was that each individual of the group had to walk for five days a week for total of six weeks.
(total 30 days in six weeks)
|
Active Comparator: Moderate physical activity (Group 2)
Female collegiate students were assessed by using Academic stress scale questionnaire, Cohen Perceived stress Scale and rapid assessment of physical activity (RAPA) to determine physical activity level and academic stress.
They were assigned into moderate Physical activity.
Each subject in first group completed 6 weeks of exercise sessions which aimed to cope up academic stress among female collegiate students.
Each subject was evaluated for changes in symptoms in each week.
|
Each session started with brisk walk, duration of which was set to 30 minutes.
Frequency set for the session was that each individual of the group had to walk for five days a week for total of six weeks.
(total 30 days in six weeks)
|
Active Comparator: Vigorous physical activity (Group 3)
Female collegiate students were assessed by using Academic stress scale questionnaire, Cohen Perceived stress Scale and rapid assessment of physical activity (RAPA) to determine physical activity level and academic stress.
They were assigned into vigorous Physical activity.
Each subject in first group completed 6 weeks of exercise sessions which aimed to cope up academic stress among female collegiate students.
Each subject was evaluated for changes in symptoms in each week.
|
Each session started with jogging, duration of which was set to 15 minutes.
Frequency set for the session was that each individual of the group had to walk for five days a week for total of six weeks.
(total 30 days in six weeks)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Academic stress scale
Time Frame: upto 6 weeks
|
it helps in measuring the level of academic stress experienced by college students due to five types of sources viz.
Personal Inadequacy, Interactions with Peers and Teachers, Fear of Examination, Inadequate Facilities at College and Parents Expectations and SES.
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upto 6 weeks
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Rapid Assessment Physical Activity scale
Time Frame: upto 6 weeks
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Physical activity level of the patients was also observed through rapid assessment of physical activity with categories as "0" for No involvement and "1" for yes and the results showed that those who are involved in any type of physical activity have a better functional outcome.
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upto 6 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 9, 2020
Primary Completion (Actual)
June 30, 2020
Study Completion (Actual)
June 30, 2020
Study Registration Dates
First Submitted
January 6, 2020
First Submitted That Met QC Criteria
January 7, 2020
First Posted (Actual)
January 9, 2020
Study Record Updates
Last Update Posted (Actual)
July 1, 2020
Last Update Submitted That Met QC Criteria
June 29, 2020
Last Verified
June 1, 2020
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- ZIHS-1272/MS/05
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Yes
IPD Sharing Supporting Information Type
- Study Protocol
- Statistical Analysis Plan (SAP)
- Informed Consent Form (ICF)
- Clinical Study Report (CSR)
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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