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Pilates exercises in Primary Dysmenorrhea

Not Applicable
Recruiting
Conditions
Primary dysmenorrhea
Primary Dysmenorrhea.
N94.4
Registration Number
IRCT20230216057434N6
Lead Sponsor
Self funded
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
57
Inclusion Criteria

Students with Primary Dysmenorrhea
Age group 18 to 25 years
Having regular Menstrual cycles
Moderate-to-severe Primary Dysmenorrhea-associated pain, indicated by a score of =4 on a numerical rating scale
Ranging from ‘0’ (no pain) to ‘10’ (unbearable pain) for at least two previous consecutive menstrual periods

Exclusion Criteria

Menstrual cycles > 35 days apart•
Pregnant females
No pain relief with over the counter analgesics

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Assessment will be performed at 0 week (baseline) at 4t week and at completion of 8 weeks treatment. Method of measurement: McGill pain Questionnaire.
Secondary Outcome Measures
NameTimeMethod
Static Balance. Timepoint: Assessment will be performed at 0 week (baseline) at 4th week and at completion of 8 weeks treatment. Method of measurement: one leg standing test with eyes open and closed.;Dynamic balance. Timepoint: Assessment will be performed at 0 week (baseline) at 4th week and at completion of 8 weeks treatment. Method of measurement: Berge Balance Scale.;Daily Functioning. Timepoint: Assessment will be performed at 0 week (baseline) at 4th week and at completion of 8 weeks treatment. Method of measurement: Brief Pain Inventory - Short form.
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