None listed
Conditions
Interventions
Intervention1: CONVENTIONAL GROUP: Group B
Participants in the conventional exercise group will undergo a 12-week program divided into three 4-week phases. During Weeks 1 to 4 the session will begin w
Sponsors
NIL
Eligibility
Inclusion criteria
Inclusion criteria: Adolescent females aged 13 to 19 years Participants diagnosed with primary dysmenorrhea. Regular menstrual cycles (21-35 days) consistent for the past 6 months. Moderate to severe menstrual pain, defined as a pain score of 4 or less on the Visual Analog Scale (VAS). No prior engagement in structured Pilates training within the past six months. Participants willing to participate. Participants not currently using analgesic medications or other pharmacological treatments for menstrual pain management.
Exclusion criteria
Exclusion criteria: Participants with MSK disorders or conditions that may limit participation in physical exercise, for e.g., CTEV, spinal deformities, fractures etc. Participants with gynecologic diseases including endometriosis, pelvic inflammatory disease, uterine cancer, etc. Participants with infectious diseases like uterine polyps or fibroids, adenomyosis etc. Participants receiving non-pharmacological treatment for dysmenorrhea. Use of medications affecting sleep quality, mood, or pain perception. Severe psychiatric disorders, for e.g., major depressive disorder, generalized anxiety disorder etc.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual Analog Scale (VAS).Timepoint: week 0- week 12 | — |
Secondary
| Measure | Time frame |
|---|---|
| Psychological general well-being (PGWBI). Pittsburgh sleep quality index (PSQI).Timepoint: week 0 - week 12 | — |
Countries
India
Contacts
Public ContactDr Deepali Hande
Pravara Institute of Medical Sciences
Outcome results
None listed