Endometriosis. Endometriosis, unspecified
Conditions
Interventions
Intervention 1: Intervention group: The clinical trial study has a pre-test, post-test and control group with the research community of women with endometriosis. To participate in the research, first
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 49 Years
Inclusion criteria
Inclusion criteria: Written informed consent to participate in the research Women of childbearing age (15-49 years) Being Iranian and living in Mashhad Have a minimum literacy Getting married and cohabiting Absence of chronic psychiatric disorders and problems in wife and her husband (self-declaration) lack of known chronic diseases in wife and husband Having sex Diagnosis of endometriosis based on history, physical examination and clinical imaging by a physician No accidents during the last 6 months Failure to attend training or cognitive-behavioral counseling classes in the previous 6 months no addiction and alcohol in wife and husband No depression, stress or severe anxiety in a woman and her husband according to the DASS-21 scale Ability to use the Internet and cyberspace if the intervention is done virtually Failure of the person and his wife to get diseases that affect sexual function absence of menopause No history of pelvic surgery Be the only wife of her husband
Exclusion criteria
Exclusion criteria: Not participating in counseling sessions for more than two sessions and not wanting to continue the intervention Incomplete completion of the questionnaire (answering less than 10% of the questionnaire) Incidence of accidents during the study Receive another training-counseling program during the intervention period.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reproductive health. Timepoint: Before and immediately one month after the intervention. Method of measurement: Endometriosis Reproductive Health Questionnaire (ERHQ).;Sexual satisfaction. Timepoint: Before and immediately one month after the intervention. Method of measurement: Women's Sexual Satisfaction Scale Questionnaire sssw. | — |
Secondary
| Measure | Time frame |
|---|---|
| Social support. Timepoint: Before and immediately one month after the intervention. Method of measurement: Standard social support questionnaire.;Stress - Anxiety - Depression. Timepoint: Before and immediately one month after the intervention. Method of measurement: Stress-Anxiety-Depression Inventory DASS-21.;Intensity of pain. Timepoint: Before and immediately one month after the intervention. Method of measurement: Severity of pain mediated by VAS criteria. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFatemeh Erfanian
Mashhad University of Medical Sciences
Outcome results
None listed