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Comparative Effects of Aerobic Exercises and Progressive Muscle Relaxation Exercises on Pain and Quality of Life

Not Applicable
Completed
Conditions
Anxiety
Pain Syndrome
Interventions
Other: Progressive muscle relaxation
Other: Aerobic exercises
Registration Number
NCT05811455
Lead Sponsor
Riphah International University
Brief Summary

Premenstrual syndrome is the clinical condition in which reproductive age females suffer from emotional and physical symptoms not related to any disease, starting usually 5 days before the menstrual cycle for 3 consecutive cycles.

Detailed Description

Premenstrual syndrome is the clinical condition in which reproductive age females suffer from emotional and physical symptoms not related to any disease, starting usually five days before the menstrual cycle for three consecutive cycles. As menstrual cycle starts in females these symptoms vanish on 4th day of menstruation. Around 10% to 53% of female adults suffer from this condition. This condition limits activities of daily life and adversely effects the quality of life therefore, the administration of proper medical intervention is very important. Aerobic exercises and progressive muscle relaxation exercises have been effective in the treatment of premenstrual syndrome previously in a few studies. However, these two interventions have never been compared to test their effects on pain, and functional performance.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
42
Inclusion Criteria
  • Age between 18 to 40 years
  • 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
  • Females with the irregular menstrual cycle
  • 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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
group b progressive muscle relaxation exercises.Progressive muscle relaxationThe 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)
Group A: aerobic exercises.Aerobic exercisesThe 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.
Primary Outcome Measures
NameTimeMethod
• SF-36 The 36-Item Short Form Health Survey questionnaire (SF-36)6 weeks

The 36-Item Short Form Health Survey questionnaire (SF-36) is a very popular instrument for evaluating Health-Related Quality of Life. The SF-36 measures eight scales: physical functioning (PF), role physical (RP), bodily pain (BP), general health (GH), vitality (VT), social functioning (SF), role emotional (RE), and mental health (MH)

1. For Anxiety, Depression: • DASS-21 The Depression, Anxiety and Stress Scale - 21 Items (DASS-21)6 weeks

The Depression, Anxiety and Stress Scale - 21 Items (DASS-21) is a set of three self-report scales designed to measure the emotional states of depression, anxiety and stress.(16)

Numerical rating scales (NRSs)6 weeks

Numerical rating scales (NRSs) are the simplest and most commonly used scale. The numerical scale is most commonly 0 to 10, with 0 being "no pain" and 10 being "the worst pain imaginable

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Johar Institute of Professional Studies

🇵🇰

Lahore, Punjab, Pakistan

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