Sexual Dysfunction and Anorexia Nervosa

NCT ID: NCT06253403

Last Updated: 2024-02-13

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

ACTIVE_NOT_RECRUITING

Total Enrollment

89 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-05-15

Study Completion Date

2026-02-28

Brief Summary

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The objective of this observational study is to investigate the potential influence of anorexia nervosa on the sexual health of women. The primary focus is to determine the presence of sexual dysfunction in individuals with anorexia nervosa and explore any potential correlation between eating disorders and sexual dysfunction. To facilitate comparison, data from a control group comprising healthy women is incorporated alongside the clinical group data.

Detailed Description

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numerous studies indicate that women diagnosed with anorexia nervosa experience a discernible impact on their sexual well-being, often accompanied by symptoms of sexual dysfunction (SD). Such dysfunction may manifest as a diminished libido, reduced sexual desire, and challenges in achieving orgasm

Conditions

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Anorexia Nervosa

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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clinic

adult women with anorexia nervosa or actual or after stabilization

psychotherapy

Intervention Type BEHAVIORAL

psychotherapy related to sexual intervention

control

health adult women without any psychological or mental illnes

No interventions assigned to this group

Interventions

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psychotherapy

psychotherapy related to sexual intervention

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

clinic group :

* adult
* women
* diagnosis of anorexia nervosa
* from Slovakia and Czech Republic

control group:

* health women
* adult
* from Slovakia and Czech Republic

Exclusion Criteria

clinic group:

* health women
* other diagnosis or disorder
* other country

control group:

* presence of some mental illness
* other country
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Comenius University

OTHER

Sponsor Role lead

Responsible Party

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Tatiana Hess

Doctoral student, Clinical research

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Tatiana Hess

Bratislava, , Slovakia

Site Status

Countries

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Slovakia

Other Identifiers

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study1

Identifier Type: -

Identifier Source: org_study_id

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