Quality of Life
Conditions
Interventions
This is a quasi-experimental, comparative and longitudinal clinical trial using the mixed method to be carried out at the UBS located in the Jardim Oásis neighborhood, where two Family Health Strategy
(IL) Limited Information: the professional clarifies about the physiology of the sexual response and anatomy of the genitalia, guiding places of greater sensitivity
(SE) Specific Suggestion: changes in sexual behavior are advised and suggested based on the physiology of the sexual response, a change in attitude is advised so that the woman remains positive in the
(T) Sexual Therapy: referral of the patient to sexual therapy, with a specialist, in case there are more severe conflicts and in the control group group health education carried out according to the a
I02.233.332
Sponsors
Universidade Estadual do Ceará
Universidade Estadual do Ceará
Eligibility
Sex/Gender
Female
Age
20 Years to 35 Years
Inclusion criteria
Inclusion criteria: Pregnant women monitored by Family Health teams (eSF) during the data collection period; with a sexual partner; age between 20 and 35 years; who are at most 18 weeks gestational on the day of the first intervention
Exclusion criteria
Exclusion criteria: Women accompanied by high-risk prenatal care, whose pregnancy resulted from sexual violence or who experience violence by an intimate partner; who present psychic alteration in the use of medications (selective serotonin reuptake inhibitors, antipsychotics, antiepileptics, anxiolytics, antidepressants and hypotensives) because they affect the female sexual response (FEBRASGO, 2017); dropouts after starting data collection; reclassification as a high-risk pregnant woman (BRASIL, 2012); missing two or more sessions of the educational intervention; if during the intervention or data collection period the woman gives birth; come to death or miscarriage; or the pregnant woman changes her address in a way that changes the link to the Basic Health Unit (UBS)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find an improvement in the sexual function observed by comparing the data collected through the Female Sexual Function Index (FSFI) in the pre-intervention (before starting the first intervention session), four weeks after the intervention (in the last session of intervention) and three months after the last week of the intervention) | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find an improvement in the quality of sexual life observed by comparing the data collected through the Questionnaire on Sexual Quality of Life – Female (SQoL-F) in the pre-intervention (before starting the first intervention session), four weeks after the intervention (in the last intervention session) and three months after the last intervention week | — |
Countries
Brazil
Contacts
Public ContactWilson Junior de Araújo Carvalho
Universidade Estadual do Ceará
Outcome results
None listed