The Effectiveness of Online Interpersonal Relationships-Based Pyschoeducation in Increasing Sexual Interest and Arousal in Women With Sexual Interest and Arousal Disorder

NCT ID: NCT06445855

Last Updated: 2024-06-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-09-30

Study Completion Date

2025-06-30

Brief Summary

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This study will be conducted to examine the effectiveness of interpersonal relationships-based online psychoeducation developed for women with sexual interest and arousal disorders.

Detailed Description

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Female sexual interest and arousal disorders are common among sexual dysfunctions. In addition to the physical and mental health of women with sexual interest and arousal disorder, interpersonal relationships are also negatively affected. Based on this relationship, it is predicted that interpersonal relationship-based psychoeducation will be effective in the treatment of sexual interest and arousal disorder.

Interpersonal Relationship Psychotherapy or counseling is a short-term, easy, accessible approach that focuses specifically on interpersonal problems and is based on attachment theory, aiming to reduce depressive symptoms and improve interpersonal functioning.

The number of internet users and the possibilities of access to the internet are increasing significantly all over the world, and online health services via the internet are becoming widespread. Online psychoeducation inevitably takes its place in internet-based applications with technological developments.

In this context, this study will be conducted to increase the sexual interest and arousal levels of women with sexual interest and arousal disorders through online psychoeducation.

Conditions

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Sexual Arousal Disorder Sexual Desire Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

One waiting group and one experimental group
Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors
Women to be included in the study will be divided into two groups after randomization. The first group will be the experimental group and the second group will be the waiting group. The experimental group will receive 8 weeks of interpersonal relationship-based online psychotherapy.

Study Groups

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Experimental group

Women in the experimental group will receive an 8-week online intervention program based on interpersonal relationships. An internet-based intervention application will be developed for this intervention. All interventions will be implemented from this intervention.

Group Type EXPERIMENTAL

Interpersonal relationship-based intervention program

Intervention Type BEHAVIORAL

An interpersonal relations-based intervention program will be implemented with an online intervention platform.

Waiting group

After the interventions in the experimental group are completed, the intervention program will be applied to the women in the waiting group.

Group Type OTHER

Interpersonal relationship-based intervention program

Intervention Type BEHAVIORAL

An interpersonal relations-based intervention program will be implemented with an online intervention platform.

Interventions

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Interpersonal relationship-based intervention program

An interpersonal relations-based intervention program will be implemented with an online intervention platform.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* A person of female biological sex,
* Expressing difficulties in sexual interest and arousal (yes to at least three of the following criteria) (questions related to these criteria will be added to the interview form)
* Decrease/absence in frequency or intensity of sexual activity,
* Decrease/absence of sexual fantasies/erotic thoughts,
* Inability to initiate sexual intercourse with their partner,
* Lack of sexual excitement and pleasure in almost all sexual relationships (about 75%),
* Decreased/absence of sexual interest/arousal to internal or external sexual erotic stimuli (e.g. written, oral, visual),
* Decreased/absence of genital or nongenital sensations in almost all sexual relationships (approximately 75%).
* Low mean scores on the Female Sexual Function Index and Sexual Interest and Desire Inventory-Female scales (mean score on the Female Sexual Function Index below 26.55, mean score on the Sexual Interest and Desire Inventory-Female below 33)
* Have sufficient knowledge about the use of the Internet,

Exclusion Criteria

* Becoming pregnant or planning pregnancy during the psychoeducation period,
* Receive treatment for any sexual dysfunction,
* Withdrew from the study at any stage of the study,
* Women who do not attend more than one session of the psychoeducation will not be included in the study (Women who miss the weekly program of the psychoeducation will be allowed a maximum of 2 make-up sessions).
Minimum Eligible Age

18 Years

Maximum Eligible Age

47 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Marmara University

OTHER

Sponsor Role lead

Responsible Party

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Zeynep Dilşah Yılmaz

PHD Student

Responsibility Role PRINCIPAL_INVESTIGATOR

Related Links

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Other Identifiers

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Istanbul University-Cerrahpasa

Identifier Type: -

Identifier Source: org_study_id

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