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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04941014
Other study ID # HERF/REC/2021-2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 4, 2019
Est. completion date December 31, 2020

Study information

Verified date June 2021
Source Health Education Research Foundation (HERF)
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main objective of the study is to determine the effects of physical activity on quality of life among female undergraduate students


Recruitment information / eligibility

Status Completed
Enrollment 52
Est. completion date December 31, 2020
Est. primary completion date December 30, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria: -moderate level of academic stress measured on academic stress scale Exclusion Criteria: - students with diagnosed psychological disorders - systematic diseases

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Light Physical Activity
The guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform Leisure Walk for 35 minutes
Moderate Physical Activity
The guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform Brisk Walk for 30 minutes
Vigourous Physical Activity
The guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform jogging for 15 minutes

Locations

Country Name City State
Pakistan Bilquis Postgraduate College for Women Pakistan Air force (PAF) Rawalpindi

Sponsors (1)

Lead Sponsor Collaborator
Health Education Research Foundation (HERF)

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of Life (QOL), The short form (SF-36) was used to observe Quality of Life (QOL), Minimum score is 0 and maximum is 100. maximum score indicate high quality of life. A change from baseline to six weeks of intervention will be observed
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