Skip to content

The effect of multimedia health-promoting lifestyle (HPL) education on sexual function and quality of sexual life in women with type 2 diabetes

The effect of multimedia health-promoting lifestyle (HPL) education on sexual function and quality of sexual life in women with type 2 diabetes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250421065421N1
Enrollment
66
Registered
2025-12-05
Start date
2025-12-10
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Type 2 Diabetes. Type 2 Diabetes

Interventions

Intervention 1: Intervention group: The health-promoting lifestyle multimedia educational content will be delivered in four 60-minute sessions, with one session per week.Data collection: Demographic i

Sponsors

Ghoum University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 55 Years

Inclusion criteria

Inclusion criteria: Aged 20 to 55 years Being married living with a spouse throughout the study period Literate (able to read and write) At least 1 year has passed since their diabetes diagnosis, with laboratory criteria confirming FBS =126 mg/dL or HbA1C =6.5%. At least 6 months of marriage and being sexually active. A score of =18.5 on the short-form screening version of the Female Sexual Function Index (FSFI-6). Having a smart phone

Exclusion criteria

Exclusion criteria: history of severe marital conflicts based on self-report concurrent diagnosis of other medical conditions (e.g., hypertension, cardiac, hepatic, renal, or thyroid diseases). pregnancy breastfeeding menopause history of surgeries such as mastectomy. history of psychiatric disorders. spouse-related issues that may impair sexual function or the quality of the couple's sexual life (based on self-report). recent life crises (e.g., bereavement of a close family member within the past six months). use of sedatives, alcohol, or recreational drugs. use of specific medications such as oral contraceptives or corticosteroids.

Design outcomes

Primary

MeasureTime frame
Sexual function. Timepoint: before, four weeks, and twelve weeks after the intervention in two intervention and control groups. Method of measurement: Female Sexual function index Questionnaire.;Sexual quality of life. Timepoint: before, four weeks, and twelve weeks after the intervention in two intervention and control groups. Method of measurement: Sexual Quality of Life-Female Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Zolfaghari

Ghoum University of Medical Sciences

zahraazolfaghari766@gmail.com+98 51 3341 7336

Outcome results

None listed

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