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Investigating the effect of mobile phone application-based education on the health-related quality of life of women with polycystic ovary syndrome

Investigating the effect of mobile phone application-based education on the health-related quality of life of women with polycystic ovary syndrome referring to Al-Zahra Educational, remedial, and Research Center in Rasht

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251015067643N1
Enrollment
80
Registered
2026-01-05
Start date
2026-01-21
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

????? ?????? ??? ??????. Polycystic ovarian syndrome

Interventions

Intervention 1: Intervention group: The educational intervention was designed to provide educational content aimed at improving health-related quality of life over a twelve-week period. In this study,

Sponsors

Rasht University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Willingness to participate in the study literacy (ability to read and write) age between 15 and 45 years ossession of a smartphone or tablet with the Android operating system ability to use and work with a mobile phone Diagnosis of polycystic ovary syndrome was based on the Rotterdam criteria (at least two of the three criteria, including menstrual irregularities, hyperandrogenism, and polycystic ovaries on ultrasound) confirmed by a gynecologist and the participant’s medical record

Exclusion criteria

Exclusion criteria: Participants with diabetes, hypertension, cardiovascular disease, or other similar conditions those who use psychiatric medications individuals with severe disabilities preventing self-care (as reported by the participant or documented in medical records) those currently participating in other educational intervention programs for polycystic ovary syndrome Pregnancy (personal report)

Design outcomes

Primary

MeasureTime frame
Health-related quality of life. Timepoint: At the baseline (pre-intervention phase) and at the twelfth week after completion of the intervention. Method of measurement: Health-related quality of life questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMona Rahnavardi

Rasht University of Medical Sciences

mona.rahnavardi@yahoo.com?+98 13 3255 3202

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026