Investigating the effect of implementing Levantal's self-regulation model on sexual function and satisfaction of women with diabetes in Qazvin city.
Conditions
Interventions
Intervention 1: Intervention group: in the test group, in addition to receiving the usual care and training, their counseling needs are first determined and a counseling program is designed based on t
Sponsors
Qazvin University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 49 Years
Inclusion criteria
Inclusion criteria: Willingness to participate in the study Age 15-49 years Living in Qazvin province At the time of study, be married and have sex Minimum literacy Ability to verbally communicate and answer questionnaire questions Having type 1 or type 2 diabetes according to expert opinion and laboratory factors (recorded in the medical record) not pregnant At least 6 months have passed since the diagnosis of diabetes
Exclusion criteria
Exclusion criteria: Any physical illness with a doctor's approval in the person or partner that affects their sexual function or sexual satisfaction Taking any type of medicine that (according to the patient) is effective on the patient's sexual function. Participation in other sexual education or counseling sessions during the last month or at the beginning of the study The existence of marital problems that affect people's sexual relations. Patients with severe psychiatric disorders that require drug therapy (clinical and semi-clinical disorders)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual performance and sexual satisfaction. Timepoint: Before the start of the intervention, after that one month, two months and three months after the intervention. Method of measurement: Demographic and Fertility Questionnaire, Sexual Function Questionnaire (FSFI), Sexual Satisfaction Questionnaire (SSS-W), Disease Perception Questionnaire (IPQ-R) and Diabetes Severity Index (DCSI). | — |
Secondary
| Measure | Time frame |
|---|---|
| Determining and comparing the level of understanding of the disease in women with diabetes in the control and test groups before and after the intervention. Timepoint: Before the intervention, one month, two months and three months after the intervention. Method of measurement: Illness perception will be measured with the Illness Perception Questionnaire (IPQ-R). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactLeila Ghorbani
Qazvin University of Medical Sciences
Outcome results
None listed