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effect of the PLISSIT model on the sexual quality of life in infertile women with sexual dysfunction

effect of the PLISSIT model on the sexual quality of life in infertile women with sexual dysfunction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230205057328N1
Enrollment
82
Registered
2023-02-14
Start date
2023-02-14
Completion date
Unknown
Last updated
2023-03-13

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

Conditions

Condition 1: Sexual dysfunction. Condition 2: Infertility. Sexual dysfunction not due to a substance or known physiological condition Female infertility

Interventions

Intervention 1: Intervention group: Individual sexual counseling based on the 4 steps of the PLISSIT model in the form of 4 weekly counseling sessions or more depending on the needs of the participant

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Be Iranian Age range from 18 to 45 years Having at least reading and writing literacy The treatment process of infertile women should be in the stage before assisted reproductive treatments having sexual dysfunction based on the score obtained from the standard FSFI questionnaire (score less than 28 from the FSFI questionnaire)

Exclusion criteria

Exclusion criteria: Husband suffering from erectile dysfunction and premature ejaculation suffering from known mental and physical diseases affecting sexual function such as diabetes, hypertension, rheumatoid arthritis, depression, etc. based on the documents included in the patient's file taking drugs that affect sexual function, such as cardiac drugs and beta blockers, H2 blockers, antidepressants, anticholinergics, and continuous use of antihistamines based on the patient's statements or the documents included in the patient's file history of participation in training classes or counseling sessions focused on sexual performance

Design outcomes

Primary

MeasureTime frame
Sexual quality of life. Timepoint: Before the intervention and 4 weeks after the intervention. Method of measurement: Sexual quality of life -female questionnaire.;Sexual function index. Timepoint: Before the intervention and 4 weeks after the intervention. Method of measurement: Female sexual function index questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReyhaneh Amini

Esfahan University of Medical Sciences

reyhane.aminiiiiii@gmail.com+98 31 3792 3071

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 5, 2026