Human papilloma virus (HPV) infection. Cervical high risk human papillomavirus (HPV) DNA test positive
Conditions
Interventions
Intervention 1: Intervention group: They receive 6 group and face-to-face counseling sessions, one 90-minute session per week. Intervention 2: Control group: There is no intervention for the control g
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Positive HPV test confirmed by gynecological oncology specialist Less than 6 months have passed since the positive test result Willingness to participate in the study and complete the informed consent form Not having any neurological or mental illness Not suffering from the type Another sexually transmitted disease Being sexually active
Exclusion criteria
Exclusion criteria: Getting HPV-related cancer while studying Getting pregnant while studying If you miss more than one session and don't do your homework
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of Life. Timepoint: The first session of the intervention and 2 weeks after the completion of the intervention sessions. Method of measurement: Quality of life questionnaire (EQUALI-HPV). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAtefeh ahmadi
Kerman University of Medical Sciences
Outcome results
None listed