brast cancer. Breast, unspecified
Conditions
Interventions
Control group: only receive routine cares.
Intervention 1: Intervention group:After completing consent form by participants, Two groups will complete demographic and SQOL-F questionnaires. After Completing the questionnaire, the interventio
Intervention group:After completing consent form by participants, Two groups will complete demographic and SQOL-F questionnaires. After Completing the questionnaire, the intervention group will div
Sponsors
Vice Chancellor for research of Hamadan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
25 Years to 50 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Aged between 25 to 50 years old; married; living with her husband; Diagnosis of breast cancer at least 6 moths ago; being in stage I and II breast cancer; lack of participating in any counseling programs and training on breast cancer in the past; lack of undergoing chemotherapy. Exclusion criteria: No participate in meeting more than two sessions; Severity of disease during the study; the incidence of other serious illnesses such as: heart disease, kidney, liver and mental illness during the study; existence of other factors that will effect on sexual life of patients such as: disaster and important change in the life and marital relationships such as violence and divorce during the study, using drugs that interfere with sexual activity, drug addiction and so on.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual quality of life in breast cancer. Timepoint: Before and two months after intervention. Method of measurement: Sexual Quality of Life Questionnaire (SQOL-F). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Parisa Parsa
Hamadan University of Medical Sciences
Outcome results
None listed