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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06253403
Other study ID # study1
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date May 15, 2023
Est. completion date February 2026

Study information

Verified date February 2024
Source Comenius University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Description:

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


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 89
Est. completion date February 2026
Est. primary completion date January 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
psychotherapy
psychotherapy related to sexual intervention

Locations

Country Name City State
Slovakia Tatiana Hess Bratislava

Sponsors (1)

Lead Sponsor Collaborator
Comenius University

Country where clinical trial is conducted

Slovakia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Female Sexual function index (FSFI) A self-administered questionnaire was utilized to gather information on participants' sexual experiences and satisfaction over the past four weeks. The questionnaire encompasses six domains: desire, arousal, lubrication, orgasm, satisfaction, and pain, each rated on a scale of 0 to 5. A lower score indicates a higher likelihood of sexual dysfunction.The maximum attainable score is 36 and minimum is 2, with a cut off of 26 serving as a potential diagnostic threshold for sexual dysfunction 1 day
Secondary The Eating Disorder Examination - Questionnaire Short (EDE-QS The Eating Disorder Examination - Questionnaire Short (EDE-QS) is a concise 12-item version featuring a 4-point response scale. The maximum attainable score is 36 and minimum is 0, with a cut off of 15 serving as a potential diagnostic threshold for eating disorder. Higher score indicate worse outcome.This instrument is designed to assess eating disorder (ED) symptoms observed within the preceding 7 days. The screening EDE-QS aims to efficiently identify probable ED symptomatology while demonstrating robust psychometric properties. 1 day
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