Effectiveness of Body- Mind Intervention in Virtual and Face to Face Method on Quality of Life in Polycystic Ovary Syndrome

Not Applicable

• Conditions: polycystic ovarian syndrome.; Polycystic ovarian syndrome; E28.2

• Registration Number: IRCT20190916044783N1
• Lead Sponsor: Vice chancellor for research, Yazd University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2021

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

Married women of childbearing age
Iranian ethnicity
Literacy for reading and writing
Internet literacy and android or i o s mobile phone for both group
Having a pco case based on Rotterdam criteria and being treated at a diabetes clinic
Having a tendency to do FBS test before study and after 8 week
Willingness to participate in the study

Exclusion Criteria

pregnancy

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Quality of Life in Patients with Polycystic Ovary Syndrome. Timepoint: Evaluation of quality of life in patients with polycystic ovary syndrome before study and after 8 and 12 weeks. Method of measurement: Iranian Amini et al. Quality of Life Questionnaire.

Secondary Outcome Measures

Name	Time	Method
Fasting blood sugar. Timepoint: At the beginning of the study and after the end of week 8. Method of measurement: Glucometer device.