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Effect of couples relationship enhancement counseling program on sexual function, sexual life quality and sexual satisfaction in women with type 2 diabetes

Effect of couples relationship enhancement counseling program on sexual function, sexual life quality and sexual satisfaction in women with type 2 diabetes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240415061491N1
Enrollment
46
Registered
2024-05-10
Start date
2024-05-21
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Diabetes. Diabetes mellitus due to underlying condition

Interventions

Sponsors

Ghoum University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 55 Years

Inclusion criteria

Inclusion criteria: 35 to 55 years old Being married and having a sexual partner Being literate in reading and writing At least one year has passed since their illness and they have laboratory criteria with FBS = 126 or HbA1C = 6.5 Good blood sugar control status (average FBS = 130 mg/dL in the last three months) Having sexual activity during the last 6 months or at least six months of cohabitation People who answered positively to at least one of the questions in the sex screening form

Exclusion criteria

Exclusion criteria: Attending another study at the same time History of participating in psychological training classes aimed at improving sexual problems History of psychiatric disorders Experiencing recent crises in life Using any type of sedative, alcohol and drugs in couples History of severe marital disputes and going to court Breastfeeding Menopause History of mastectomy or complete hysterectomy History of psychiatric disorders Suffering from other acute or chronic diseases in couples (blood pressure, heart, kidney, liver and thyroid diseases) Use of oral contraceptives and corticosteroids

Design outcomes

Primary

MeasureTime frame
Quality of sexual life. Timepoint: Before, 2 weeks and 12 weeks after participating in the meetings in two intervention and control groups. Method of measurement: Women's sexual life quality questionnaire.;Sexual satisfaction. Timepoint: Before, 2 weeks and 12 weeks after participating in the meetings in two intervention and control groups. Method of measurement: Larson's sexual satisfaction questionnaire.;Sexual performance. Timepoint: Before, 2 weeks and 12 weeks after participating in the meetings in two intervention and control groups. Method of measurement: Women's sexual performance scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohre Khalajinia

Ghoum University of Medical Sciences

zkh6033@yahoo.com+98 25 3778 0001

Outcome results

None listed

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