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The effect of the educational program on quality of life in PCOS women

The effect of the educational program on quality of life in PCOS women in intervention and control groups

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201308289463N15
Enrollment
110
Registered
2017-11-05
Start date
2017-11-11
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Quality of life in PCOS women. Polycystic ovarian syndrome

Interventions

Intervention 1: Intervention:In The sexual education program once a week for 4 weeks will be given. The quality of life will be measured by PCOSQ before the intervention, two weeks after the interven
Treatment - Drugs
Intervention:In The sexual education program once a week for 4 weeks will be given. The quality of life will be measured by PCOSQ before the intervention, two weeks after the intervention and 3 month
Control: In control group the education program not will be prescribed. The quality of life will be measured by PCOSQ before the study,two weeks after the study and 3 months after the study. In order

Sponsors

Vice chancellor for research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: A confirmed case of PCOS was diagnosed based on the case definition of the Rotterdam diagnostic criteria; being 18-45 years of age; married; Sexual Dysfunction (having a score of 28 and less in the Female Sexual Function Index questionnaire; no sexual problem or disabling disease in the spouse; not being previously diagnosed with psychiatric disorders and not using psychiatric medications; do not suffer from other chronic diseases affecting the quality of life; being able to read and write. Exclusion criteria: unwillingness to continue cooperation; the emergence of any known physical or psychological illness that affects the quality of life; occurrence of pregnancy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Health related quality of life. Timepoint: before the intervention, two weeks after intervention, 3 months after the intervention. Method of measurement: PCOSQ or Cronin Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBita Fereidooni

Tehran University of Medical Science

barshimah@yahoo.com+98 818211025

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026