Investigating the effect of increasing awareness based on Acceptance and Commitment Therapy on the quality of life of women with HPV

Not Applicable

Recruiting

• Conditions: Human papilloma virus (HPV) infection.; Cervical high risk human papillomavirus (HPV) DNA test positive; R87.810

• Registration Number: IRCT20170611034452N16
• Lead Sponsor: Kerman University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 January 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 60

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

Getting HPV-related cancer while studying
Getting pregnant while studying
If you miss more than one session and don't do your homework

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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).