Actively Recruiting

Phase Not Applicable
Age: 18Years - 59Years
FEMALE
Healthy Volunteers
NCT02613546

THE INFLUENCE OF COGNITIVE BEHAVIORAL THERAPY IN SEXUAL DYSFUNCTION FEMALE: Randomized Clinical Trial

Led by Centro de Atenção ao Assoalho Pélvico · Updated on 2023-12-05

34

Participants Needed

1

Research Sites

585 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research is a randomized clinical trial aims to evaluate the influence of cognitive-behavioral psychotherapy (CBT) on quality of life and sexual function of patients with sexual dysfunction. The notion of sexual health for the World Health Organization exceeds the concept of sickness absence, having a subjective well-being of significance in the spheres of self-concept, self-image, interpersonal relationships and sense of self worth. Furthermore, sexual satisfaction and relationship quality of life is also evidenced in many studies. CBT is a brief and focal psychotherapy with proven efficacy in several mental disorders, improving health and quality of life of the treated populations. However, they did not find clinical trials that showed the effectiveness of CBT in Sexual Dysfunctions. This study aims to then fill this gap by evaluating the relationship from the use of techniques of CBT.

CONDITIONS

Official Title

THE INFLUENCE OF COGNITIVE BEHAVIORAL THERAPY IN SEXUAL DYSFUNCTION FEMALE: Randomized Clinical Trial

Who Can Participate

Age: 18Years - 59Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged 18-59 years
  • Female Sexual Function Index (FSFI) score less than or equal to 26
Not Eligible

You will not qualify if you...

  • Moderate or severe scores on Beck Scales
  • Started hormone therapy after joining the group

AI-Screening

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Trial Site Locations

Total: 1 location

1

Centro de Atenção ao Assoalho Pelvico

Salvador, Estado de Bahia, Brazil, 40.290-000

Actively Recruiting

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Research Team

P

Patricia V Lordelo, Phd

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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