Quality of LifeNCT04941014
Effects of Physical Activity on Quality of Life Among Female Undergraduate Students
A study testing Light Physical Activity, Moderate Physical Activity and Vigourous Physical Activity in people with Quality of Life, run by Health Education Research Foundation (HERF) at 1 site in Pakistan.
Trial summary
The main objective of the study is to determine the effects of physical activity on quality of life among female undergraduate students Read more about this study
- Who is it for?
- Ages 18 to 25 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Quality of Life
- What is being tested?
- Light Physical Activity, Moderate Physical Activity and Vigourous Physical Activity
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 52 participants
- Where
- 1 sitePakistan
- Study dates
- 4 May 2019to 31 Dec 2020
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 25 years
- Women only
- Healthy volunteers accepted
- Adult
Who may be able to join
- -moderate level of academic stress measured on academic stress scale
Who cannot join
- students with diagnosed psychological disorders
- systematic diseases
Trial locations and contacts
1 site in 1 country.
Pakistan1 site
Bilquis Postgraduate College for Women Pakistan Air force (PAF)
Rawalpindi
About this study
The main objective of the study is to determine the effects of physical activity on quality of life among female undergraduate students
- Conditions
- Quality of Life
- Being tested
- Light Physical Activity, Moderate Physical Activity, Vigourous Physical Activity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Light Physical ActivityBehavioural
The guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform Leisure Walk for 35 minutes
Moderate Physical ActivityBehavioural
The guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform Brisk Walk for 30 minutes
Vigourous Physical ActivityBehavioural
The guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform jogging for 15 minutes
| Study group | Role | What they receive |
|---|---|---|
| Light Physical Activity (LPA) | Active comparator | The guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform Leisure Walk for 35 minutes Receives: Behavioral: Light Physical Activity |
| Moderate Physical Activity (MPA) | Active comparator | The guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform Brisk Walk for 30 minutes Receives: Behavioral: Moderate Physical Activity |
| Vigorous Physical activity (VPA) | Active comparator | The guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform jogging for 15 minutes Receives: Behavioral: Vigourous Physical Activity |
What is being measured
The primary outcome is the main question the study is designed to answer.
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.
Measured: A change from baseline to six weeks of intervention will be observed
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Jun 2021
- Study start4 May 2019
- Primary completion30 Dec 2020
- Study completion31 Dec 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Quality of LifeStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Assignment
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 52 participants (actual)
Sponsor and investigators
- Lead sponsor
- Health Education Research Foundation (HERF)
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04941014
- Sponsor's protocol ID
- HERF/REC/2021-2
- Status last verified
- Jun 2021
- First submitted
- 8 Jun 2021
- Last updated
- 28 Jun 2021
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 28 Jun 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Physical Activity on Quality of Life Among Female Undergraduate Students
- ClinicalTrials.gov ID
- NCT04941014
- Acronym / sponsor ID
- HERF/REC/2021-2
- Conditions
- Quality of Life
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 52 participants (actual)
- Lead sponsor
- Health Education Research Foundation (HERF)University, hospital or other
- Study start
- 4 May 2019 (actual)
- Primary completion
- 30 Dec 2020 (actual)
- Study completion
- 31 Dec 2020 (actual)
- First posted
- 28 Jun 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The main objective of the study is to determine the effects of physical activity on quality of life among female undergraduate students
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 3
- Model description
- Assignment
| Arm | Type | Receives |
|---|---|---|
| Light Physical Activity (LPA) | Active comparator | Behavioral: Light Physical ActivityThe guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform Leisure Walk for 35 minutes |
| Moderate Physical Activity (MPA) | Active comparator | Behavioral: Moderate Physical ActivityThe guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform Brisk Walk for 30 minutes |
| Vigorous Physical activity (VPA) | Active comparator | Behavioral: Vigourous Physical ActivityThe guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform jogging for 15 minutes |
Who may qualify
- Ages
- 18 to 25 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (1 listed)
- -moderate level of academic stress measured on academic stress scale
Key exclusion criteria (2 listed)
- students with diagnosed psychological disorders
- systematic diseases
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Light Physical ActivityThe guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform Leisure Walk for 35 minutes | Behavioural | Light Physical Activity (LPA) |
| Moderate Physical ActivityThe guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform Brisk Walk for 30 minutes | Behavioural | Moderate Physical Activity (MPA) |
| Vigourous Physical ActivityThe guidelines from Rapid Assessment of Physical Activity (RAPA) participants were asked to perform jogging for 15 minutes | Behavioural | Vigorous Physical activity (VPA) |
Primary outcome
Quality of Life (QOL),
Time frame: A change from baseline to six weeks of intervention will be observed
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.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Jun 2021.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Light Physical Activity, Moderate Physical Activity and Vigourous Physical Activity in people with Quality of Life, run by Health Education Research Foundation (HERF) at 1 site in Pakistan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 28 Jun 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Quality of Life (QOL), (time frame: A change from baseline to six weeks of intervention will be observed). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Jun 2021.