Skip to content

The Effectiveness of sexual counseling using PLISSIT model on sexual quality of life and sexual function of diabetic women

The Effectiveness of sexual counseling using PLISSIT model on sexual quality of life and sexual function of women with type 2 diabetes mellitus

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017070231662N4
Enrollment
110
Registered
2017-08-02
Start date
2017-08-21
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

Diabetes. With unspecified complications

Interventions

Intervention 1: Intervention group: 55 diabetic women with at least one sexual broblem will receive three 45 minute individual sexual counseling based on PLISSIT model weekly. Contents of counseling s
Behavior
Intervention group: 55 diabetic women with at least one sexual broblem will receive three 45 minute individual sexual counseling based on PLISSIT model weekly. Contents of counseling sessions will be
Ccontrol group: 55 diabetic women with at least one sexual problem will receive a general health educational pamphlet and also one session sexual counseling.

Sponsors

Alborz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: writing and reading literacy in Persian; being sexual active; aged 35-55; having at least one sexual problem and desire to talk about that. Exclusion criteria: participating in similar classes influencing in sexual function; pregnancy during study; severe conflict in marital relationship and/ or divorce.

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
Depression. Timepoint: Before, 4 weeks and 8 weeks after intervention. Method of measurement: Beck II Depression questionnaire.

Primary

MeasureTime frame
Sexual quality of life. Timepoint: before, 4 weeks , and 8 weeks after intervention. Method of measurement: SQOL-F.;Sexual function. Timepoint: before, 4 weeks , and 8 weeks after intervention. Method of measurement: FSFI questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Mehrabi

Alborz University of Medical Sciences- School of Nursing and Midwifery

marimehrabi191@gmail.com+263 4 304 433

Outcome results

None listed

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