MedPath

Premenstrual syndrome and exercises

Phase 4
Conditions
Premenstrual syndrome
Registration Number
PACTR201908589835132
Lead Sponsor
Faculty of Physical Therapy
Brief Summary

Results revealed that the resistive group showed a highly significant decrease in premenstrual symptoms score (p=0.0001), progesterone (p=0.0001), prolactin (p=0.0001) and significant decrease in estradiol (p=0.004) post treatment. While WBV group showed a highly significant decrease in premenstrual symptoms score (p=0.0001), prolactin (p=0.001)and a significant decrease in estradiol (p=.042), progesterone (p=0.039) post-treatment. However, resistive group showed a highly significant decrease in premenstrual symptoms score (p=0.0019) and a significant decrease in estradiol (p=0.0027), progesterone (p=0.046) and prolactin (p=0.042) when compared to WBV group.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
30
Inclusion Criteria

Participants ages ranged from 16-20 years and their body mass index was <19.9kg/m2.
They experienced regular menstrual cycles.
They were diagnosed with PMS according to PMS questionnaire.

Exclusion Criteria

Females with the following criteria were excluded including a history of pelvic pathology, pelvic inflammatory diseases, endometriosis, cardiac diseases, thyroid diseases, taking oral contraceptive pills, or smoking.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Estradiol ;Progesterone;Prolactin
Secondary Outcome Measures
NameTimeMethod
Premenstrual symptoms including anxiety, depression, hyper hydration, craving and other symptoms, cramp and low back pain
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