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Efficacy of a web-based virtual clinic in the treatment of sexual dysfunction and the enhancement of the sexual quality of life for couples.

Design, implementation, and evaluation of the efficacy of web-based services for a virtual sexual health clinic on sexual dysfunction and enhancement of the sexual quality of life for couples: A randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110827007422N5
Enrollment
80
Registered
2024-07-15
Start date
2024-08-17
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Sexual dysfunction. Sexual dysfunction

Interventions

Intervention 1: Intervention Group: In this study, the intervention group will receive counseling through a website once a week for a minimum of 60-90 minutes using the Plissit model for one month. Th

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 49 Years

Inclusion criteria

Inclusion criteria: Willingness to participate in the study Presence of sexual dysfunction in one or both partners Access to the internet, smartphone, and computer Ability to navigate websites Living with one's spouse Absence of psychological disorders No use of neurologic or psychiatric medications Absence of other chronic physical illnesses At least one year since their marriage Age between 18 to 49 years Married and sexually active Couples without any other temporary partners

Exclusion criteria

Exclusion criteria: Participation in educational and counseling sessions related to improving sexual performance during the past 6 months Pregnancy or breastfeeding Infertility Participation in other psychological interventions after entering the study Absence of more than 1 session in counseling meetings Scoring 23 or higher on the Goldberg General Health Questionnaire

Design outcomes

Primary

MeasureTime frame
Sexual dysfunction. Timepoint: Before the intervention, Immediately After the Intervention, one Month After the Intervention. Method of measurement: The Female Sexual Function Index (FSFI)-The International Index of Erectile Function (IIEF).;Quality of sexual life. Timepoint: Before the intervention, Immediately After the Intervention, one Month After the Intervention. Method of measurement: The sexual quality of life-female (SQOL-F) questionnaire-Sexual Quality of Life - Men,(SQOL-M).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Jila Ganji

Mazandaran University of Medical Sciences

zhila.ganji@yahoo.com+98 11 3325 7230

Outcome results

None listed

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