Evaluation of the effectiveness of Psycho-educational Intervention in the treatment of disorders in the sexual performance in women: a randomized clinical trial
Not Applicable
Recruiting
- Conditions
- ack or loss of sexual desire. Orgasmic disorder. Dyspareunia
- Registration Number
- RBR-10gn5jbj
- Lead Sponsor
- niversidade Federal do Maranhão
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
sexually active women; 18 to 45 years old; with sexual dysfunction according to the FSFI instrument; score less than or equal 26
Exclusion Criteria
women under the age of 18 who has any of the following morbidities;Diabetes; arterial hypertension; thyroid diseases such as neuropathies; depression; hyperprolactinemia; hypoandrogenism; vaginismus; or use of benzodiazepines; antidepressants; antidopaminergic antipsychotics; antiandrogens; beta adrenergic blockers; centrally acting antihypertensives; histamine H2 blockers ; or that report the presence of a third persons at the place of sexual intercourse
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome will be the proportion comparasion of participants who present FSFI scores above 26, assessed 60 days after the 1st intervention, in both groups, Experimental Group and Control Group, in two moments, pre (first contact) and post-intervention (60 days) through the FSFI.
- Secondary Outcome Measures
Name Time Method Proportion comparasion of participants with a Dyadic Adjustment Scale (EAD) score >101 points in both groups, Experimental Group and Control Group, in two moments, pre (first contact) and post-intervention (60 days).;Comparison of mean quality of life according to the WHOQOL-26 questionnaire in both groups, Experimental Group and Control Group, in two moments, pre (first contact) and post-intervention (60 days).