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The Comparison between the Effect of PLISSIT and Sexual Health Model on the Sexual Function and Sexual quality of life in menopause

The Comparison between the Effectiveness of PLISSIT and Sexual Health Model on the Sexual Function and Sexual quality of life in menopause: A Randomized Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230808059085N1
Enrollment
105
Registered
2023-09-11
Start date
2023-09-17
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Sexual issues.

Interventions

Intervention 1: Intervention group: PLISSIT. Counseling will be done in three face-to-face and individual sessions and the duration of the sessions will be 60-90 minutes.The first stage of counseling

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 64 Years

Inclusion criteria

Inclusion criteria: being married, Being literate in reading and writing, Being sexually active in the last month, Age range between 40_64, Menopause has occurred naturally, At least one year has passed since their menopause, Absence or history of known mental and physical illness that has a negative impact on sexual relations, Not taking drugs to reduce sexual desire, Do not use addictive substances and alcohol, No history of hysterectomy, Not having an adverse event within 3 months before the start of the intervention, Not having extramarital relations of each couple, Not participating in sex education classes or receiving sex counseling services

Exclusion criteria

Exclusion criteria: Failure to participate in more than one intervention session, Marital discord, death or divorce during intervention, Performing surgery during intervention

Design outcomes

Primary

MeasureTime frame
Female sexual function. Timepoint: Before, 4 and 6 weeks after the intervention. Method of measurement: Female Sexual Function questionnaire.;Sexual Quality Of Life. Timepoint: Before, 4 and 6 weeks after the intervention. Method of measurement: Sexual Quality Of Life Questionnaire-Female.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactzahrazamiriaraste

Shahid Beheshti University of Medical Sciences

zahrazamiriaraste1997@yahoo.com+98 21 8865 5366

Outcome results

None listed

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