MedDataX Logo

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

NCT ID: NCT02613546

Last Updated: 2023-12-05

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

34 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-09-10

Study Completion Date

2026-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Sexual Dysfunctions

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

cognitive-behavioral psychotherapy Sexual Dysfunctions Women

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Cognitive behavioral therapy (CBT)

The study group will undergo 10 sessions of guidelines and cognitive behavioral therapy (CBT) about an hour long, once a week. Of these:

1. evaluation session;
2. sessions of psychoeducation about the CBT model

5 sessions of cognitive restructuring 2 sessions of preventing relapse

Group Type EXPERIMENTAL

Cognitive behavioral therapy (CBT)

Intervention Type BEHAVIORAL

The study group will undergo 10 sessions of guidelines and cognitive behavioral therapy (CBT) about an hour long, once a week. Of these:

1. evaluation session;
2. sessions of psychoeducation about the CBT model

5 sessions of cognitive restructuring 2 sessions of preventing relapse

Control

The control group will be subjected to 10 weekly sessions (1 time per week) approximately one hour guidelines.

Group Type OTHER

Control therapy

Intervention Type BEHAVIORAL

The control group will be subjected to 10 weekly sessions (1 time per week) approximately one hour guidelines.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Cognitive behavioral therapy (CBT)

The study group will undergo 10 sessions of guidelines and cognitive behavioral therapy (CBT) about an hour long, once a week. Of these:

1. evaluation session;
2. sessions of psychoeducation about the CBT model

5 sessions of cognitive restructuring 2 sessions of preventing relapse

Intervention Type BEHAVIORAL

Control therapy

The control group will be subjected to 10 weekly sessions (1 time per week) approximately one hour guidelines.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Women aged 18-59 years;
* FSFI less than or equal to 26.

Exclusion Criteria

* Scores of Beck Scales - moderate or severe;
* Prescribing hormone therapy after starting the group.
Minimum Eligible Age

18 Years

Maximum Eligible Age

59 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Centro de Atenção ao Assoalho Pélvico

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Patricia V Lordelo, PhD

Role: PRINCIPAL_INVESTIGATOR

Centro de Atenção ao Assoalho Pélvico - BAHIANA

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Centro de Atenção ao Assoalho Pelvico

Salvador, Estado de Bahia, Brazil

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Brazil

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Patricia V Lordelo, Phd

Role: CONTACT

Phone: +5571988592400

Email: [email protected]

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Patricia V Lordelo, Phd

Role: primary

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

U1111-11754978

Identifier Type: -

Identifier Source: org_study_id