Sexual health empowerment model versus DEEP model (Natural Differences, Emotional Sensitivities, External Stressors, Patterns of Communication) on sexual function and attitude and performance of condom use in Papillomavirus infected wome

Not Applicable

Recruiting

Conditions: Human Papilloma Virus.
Papillomavirus as the cause of diseases classified elsewhere
B97.7

Registration Number: IRCT20230710058738N1

Lead Sponsor: Yazd University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Female

Target Recruitment: 68

Inclusion Criteria

Having a medical record of being infected with papillomavirus (infection with low-risk or high-risk types of the virus and type 1 and 2 dysplasia) at Baghaeipour Clinic in Yazd, diagnosed by the physician
Women in reproductive age (15 to 49 years)
Being married
Having sufficient sexual intercourse with the spouse in the past 4 weeks
Willingness to participate in the study
Owning an Android or iOS smartphone
Being able to use online counseling via a smartphone
Literacy in reading and writing
Proficiency in speaking Persian
Sexual dysfunction

Exclusion Criteria

Pregnancy
Condom use
Diagnosis of psychological disorders in the past year according to women's statements
Participation in similar studies
Occurrence of stressful events during participation in the study (such as the death of family members or divorce)
Addiction to drugs and alcohol
Patients with hearing problems

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sexual function (primary outcome variable). Timepoint: Baseline, completion of the intervention in the eighth week and follow-up at the end of the study in the twelfth week. Method of measurement: Rosen et al Sexual Functioning Questionnaire (1997).

Secondary Outcome Measures

Name	Time	Method
Attitude toward condom use (Secondary outcome variable). Timepoint: Baseline, completion of the intervention in the eighth week and follow-up at the end of the study in the twelfth week. Method of measurement: Attitude of Condom Use Questionnaire.;The frequency of condom use (Secondary outcome variable). Timepoint: Baseline, completion of the intervention in the eighth week and follow-up at the end of the study in the twelfth week. Method of measurement: Performance of Condom Use Questionnaire.