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The effect of acupressure on quality of life in patients with polycystic ovarian syndrome

Not Applicable
Conditions
Polycystic ovary syndrome.
Polycystic ovarian syndrome
E28.2
Registration Number
IRCT20180725040587N1
Lead Sponsor
Yasouj University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
96
Inclusion Criteria

By the gynecologist, polycystic ovarian syndrome has been confirmed
Marital status
Earning the minimum basic score (1.3 points for the correction version of the quality of life questionnaire related to health of polycystic ovary syndrome), Quality of life questionnaire 12 questions, minimum score 24-12
Absence of male infertility (confirmed by spermogram test)
Having ages 45-15 years

Exclusion Criteria

Having any systemic or endocrine and neurological disease based on the patient's question including: cardiovascular disease, type 1 and type 2 diabetes, neoplastic diseases including Cushing's syndrome, congenital adrenal hyperplasia and hyperprolactinemia (approved by a specialist)
Addiction to hookah, cigarettes, drugs and alcohol according to the research unit
Taking any hormonal medication except clomiphene
Presence of male infertility (confirmed by spermogram test)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Quality of Life in Patients with Polycystic Ovary Syndrome. Timepoint: Before the intervention, three months after the intervention. Method of measurement: Modified Polycystic Ovary Syndrome Health-Related Quality Of Life Questionnaire (MPCOSQ) ?Short Form12 (SF-12).
Secondary Outcome Measures
NameTimeMethod
Hirsutism. Timepoint: Before intervention, three months after the intervention. Method of measurement: Friedman Galway Scale.;Acne. Timepoint: Before intervention, three months after the intervention. Method of measurement: Global Acne Grading System (GAGS).;Alopecia. Timepoint: Before intervention, three months after the intervention. Method of measurement: Ludwig scale.;Total Testosterone. Timepoint: Before intervention, three months after the intervention. Method of measurement: NG/L.
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