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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06187246
Other study ID # UniversidadRJC 2005202114121
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2022
Est. completion date June 1, 2023

Study information

Verified date December 2023
Source Universidad Rey Juan Carlos
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A randomized controlled trial was conducted for testing the efficacy of a novel avatar-based intervention (IG), that was compared with a control group (CG) for women with female orgasmic disorder (FOD). Participants were 31 women who were randomly assigned to the intervention or the control conditions. Intervention was based on the cognitive behavioral therapy approach (treatment with the most empirical evidence) and previous literature about FOD. It consisted of 12 weekly online individual sessions and aimed at improving the FOD diagnosis, sexual variables, and variables that are known to affect orgasm consecution. Control group was based on minimum therapeutic contact. Changes over time in the assessed variables were analyzed using linear mixed models, considering treatment group, measurement time point, and group-by-time interactions as fixed effects. Effect sizes were computed (Cohen's d; number needed to treat - NNT; reliable change index - RCI).


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date June 1, 2023
Est. primary completion date June 1, 2023
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Present the characteristics to diagnose female orgasm disorder after a clinic assessment (considering natural characteristics of the women's sexual response cycle (Conn & Hodges, 2022) based on the DSM-5 criteria. - Provide a medical check to prove the absence of physical factors that may be the cause of the orgasm dysfunction, as this is the first part to diagnose FOD. - Be at least 18 years old (adult). - Have access to a computer with the characteristics to run Second Life and internet connection. Exclusion Criteria: - Present a diagnosis of a physical condition that may be the cause of the orgasm dysfunction (e.g., genital lesions, systemic and hormonal factors, vulvovaginal atrophy). - Presence of other psychological pathology (e.g., depression, trauma) that may be the cause of the orgasm dysfunction. - Have alcohol dependence (i.e., evaluated during the clinical assessment, according to the diagnostic criteria from the DSM-5, to determine if the individual meets the criteria for an alcohol use disorder diagnosis). - Drug use, including medication that is known to cause sexual difficulties (e.g., selective serotonin reuptake inhibitors (SSRIs), that are a particularly common drug cause of sexual dysfunction. - Have participated in a previous psychological intervention in the last year.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Avatar-based intervention
Intervention was aimed at improving sexual variables (sexual satisfaction, sexual function, and initiative and sexual communication), and variables that are known to affect orgasm consecution (sexual self-esteem, sex-guilt, and sexual anxiety). To achieve this objective, it focused on fostering participants' abilities to increase their levels of sexual stimulation, and the engagement in personal values, along with identifying and modifying dysfunctional thoughts about sexuality. The techniques used included psychosexual education, cognitive restructuring, virtual exposure, sexual stimulation, and engagement in personal values from the acceptance and commitment therapy (ACT) perspective. It was delivered via a metaverse: Second Life.
Other:
Individual informative talks
Participants were provided with information about female orgasm (e.g., what is an orgasm, neuronal orgasm, factors that may influence consecution, sexual response), masturbatory techniques (e.g., key elements to achieve pleasure, anatomy of the female genitalia, pleasure areas) and techniques to focus attention on one's body (i.e., an important factor to pleasure). Participants received three individual sessions once a month, and had a duration of one hour.

Locations

Country Name City State
Spain Rey Juan Carlos University Alcorcon Madrid

Sponsors (1)

Lead Sponsor Collaborator
Universidad Rey Juan Carlos

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sexual satisfaction assessed by the Golombok Rust Inventory of Sexual Satisfaction Sexual satisfaction is the feeling of pleasure that one has when the sexual desire has been fulfilled.
The Golombok Rust Inventory of Sexual Satisfaction has minimum-maximum values of 0-112; higher scores mean a worse outcome. The cut-off for determining significant levels of Sexual Satisfaction is 60 (scores equal to or above 60 indicate the existence of a sexual problem).
From baseline to the end of the treatment at 12 weeks + 1 month-follow-up and 3 month-follow-up
Primary Sexual functionassessed by the Female Sexual Function Index Sexual function refers to the capacity of having a satisfactory sexual life. The Female Sexual Function Index has minimum-maximum values of 19-95; higher scores mean a better outcome. The cut-off for determining signi?cant levels of this variable is 55 (scores equal to or below 55 indicate poor Sexual Function). From baseline to the end of the treatment at 12 weeks + 1 month-follow-up and 3 month-follow-up
Primary Initiative and Sexual Communication assessed by the Female Sexual Function Questionnaire Initiative and Sexual Communication is the proactive and consensual expression of one's sexual desires, interests, and intentions within the context of a sexual relationship or encounter.
The Female Sexual Function Questionnaire has minimum-maximum values of 14-70; higher scores mean a better outcome. The cut-off for determining significantly low levels of this variable are scores equal to or lower than 25.
From baseline to the end of the treatment at 12 weeks + 1 month-follow-up and 3 month-follow-up
Secondary Sexual self-esteem assessed by the Rosenberg Self-Esteem Scale Self-esteem related to sexuality; may influence on the consecution of orgasms. The Rosenberg Self-Esteem Scale has minimum-maximum values of 10-40; higher scores mean a better outcome. The cut-off for clinical low self-esteem is a score equal to or lower than 25. From baseline to the end of the treatment at 12 weeks + 1 month-follow-up and 3 month-follow-up
Secondary Sex-guilt assessed by the Brief Mosher Sex-Guilt Scale Sex-guilt related to sexuality; may influence on the consecution of orgasms. The Brief Mosher Sex-Guilt Scale has minimum-maximum values of 10-60; higher scores mean a worse outcome (higher scores indicate higher levels of guilt). From baseline to the end of the treatment at 12 weeks + 1 month-follow-up and 3 month-follow-up
Secondary Sexual anxiety by the Sexual Anxiety scale of the Expanded Sexual Arousability Inventory Sexual anxiety related to sexualiaty; may influence on the consecution of orgasms.
TheSexual Anxiety scale of the Expanded Sexual Arousability Inventory has minimum-maximum values of 0-168; higher scores mean a worse outcome (higher scores indicate higher levels of sexual anxiety).
From baseline to the end of the treatment at 12 weeks + 1 month-follow-up and 3 month-follow-up
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