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 women

The effectiveness comparison of sexual health empowerment model via DEEP model (Natural Differences, Emotional Sensitivities, External Stressors, Patterns of Communication) on sexual function and attitude and performance of condom use in papillomavirus infected women

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230710058738N1

Enrollment

Registered

2023-08-22

Start date

2023-10-02

Completion date

Unknown

Last updated

2023-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Human Papilloma Virus. Papillomavirus as the cause of diseases classified elsewhere

Interventions

Intervention 1: The first intervention group: The first group will receive the DEEP model in the form of 8 online and consecutive sessions, once a week for 90 minutes, by the second researcher, a seni

Eligibility

Sex/Gender

Female

Age

15 Years to 49 Years

Inclusion criteria

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

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

Design outcomes

Primary

Measure	Time frame
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

Measure	Time frame
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.	—

Measure

Time frame

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.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTahmineh Farajkhoda

Yazd University of Medical Sciences

farajkhoda_t@yahoo.com+98 35 3824 1751

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026