sexual health. Other sexual dysfunction not due to a substance or known physiological condition
Conditions
Interventions
Intervention group: Intervention group: At first, the questionnaires of personal information, sexual self-concept, sexual quality of life and DASS-21 scale are completed by the research units. Then, i
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Having written consent to participate in the study Having the least reading and writing literacy Primiparous women in 2 to 6 months after childbirth Having Iranian citizenship 18 to 35 years old Her recent delivery was non-traumatic and the result is a healthy singleton baby Being married and the only wife of her husband Currently living with her husband and have resumed her sexual relationship after childbirth (having sex at least once or twice a week)
Exclusion criteria
Exclusion criteria: Suffering from chronic diseases affecting sexual issues Addiction to alcohol, drugs and other psychoactive drugs Suffering from severe psychiatric diseases Participating in sexual training or counseling Taking drugs affecting sexual function in a woman or her husband The presence of prostate problems and sexual disorders in the husband Have a history of pelvic surgery or radiotherapy Suffering from severe depression, anxiety and stress
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual self-concept score based on MSSCQ questionnaire. Timepoint: At the beginning of the study (before the implementation of the intervention), immediately and 2 months after the last session of the intervention. Method of measurement: Snell sexual self-concept questionnaire.;Sexual quality of life score based on SQOL-F questionnaire. Timepoint: At the beginning of the study (before the implementation of the intervention), immediately and 2 months after the last session of the intervention. Method of measurement: Symonds sexual quality of life questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Sexual function score based on FSFI questionnaire. Timepoint: At the beginning of the study (before the implementation of the intervention), immediately and 2 months after the last session of the intervention. Method of measurement: Rosen sexual function questionnaire (FSFI). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactRahele Babazade
Mashhad University of Medical Sciences
Outcome results
None listed