Comparative Effects of Aerobic Exercises and Progressive Muscle Relaxation Exercises on Pain and Quality of Life
NCT ID: NCT05811455
Last Updated: 2023-04-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
42 participants
INTERVENTIONAL
2022-11-02
2023-01-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Group A: aerobic exercises.
The first treatment group will be given aerobic exercises for six weeks at least three times per week. This group will include 14 participants. This study group will be assigned with basic treatment protocol with aerobic exercises along with 10 minutes of warm up period.
Aerobic exercises
To compare the effects of aerobic exercise and progressive muscle relaxation exercises on pain and quality of life in premenstrual syndrome
group b progressive muscle relaxation exercises.
The intervention will be given three days per week for six weeks. Pre and post-treatment readings will be noted. Each total session will last for 45 minutes. The importance of the study will be explained, and consent will be taken from the people before the intervention will be applied.
* Breathe in, and tense the first muscle group (hard but not to the point of pain or cramping) for 4 to 10 seconds.
* Breathe out, and suddenly and completely relax the muscle group (do not relax it gradually) (20)
Progressive muscle relaxation
progressive muscle relaxation exercises.
Group C. Control group
No intervention was given
No interventions assigned to this group
Interventions
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Aerobic exercises
To compare the effects of aerobic exercise and progressive muscle relaxation exercises on pain and quality of life in premenstrual syndrome
Progressive muscle relaxation
progressive muscle relaxation exercises.
Eligibility Criteria
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Inclusion Criteria
* Females in their last week of the luteal phase (1 week before menstruation)
* Females with regular menstrual with equal intervals between 21 and 35 days
* Females with a score of 133 and above after being screened with Premenstrual syndrome scale
* Females suffering from PMS for at least the past six months
Exclusion Criteria
* Pregnant females
* Menstruating females or females in the follicular or ovulatory phase
* History of physical exercise in the past three months before the beginning of the study
* Females suffering from other gynecological issues such as endometriosis, PCOS, uterine or cervical cancer
18 Years
40 Years
FEMALE
Yes
Sponsors
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Riphah International University
OTHER
Responsible Party
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Principal Investigators
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Fatima Tariq, Mphill
Role: PRINCIPAL_INVESTIGATOR
Riphah International University
Locations
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Johar Institute of Professional Studies
Lahore, Punjab Province, Pakistan
Countries
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Other Identifiers
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REC/RCR & AHS/22/054
Identifier Type: -
Identifier Source: org_study_id
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