An abnormal Pap smear and the impact of notification manner on women’s health-related quality of life, coping and awareness of human papillomavirus

Completed

• Conditions: An abnormal Pap smear result. Diagnosed as ASC-US+HR-HPV, LSIL+HR-HPV or HSIL.; Urological and Genital Diseases; Abnormal Pap smear result

• Registration Number: ISRCTN80102009
• Lead Sponsor: Kamprad Family Foundation

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2017-05-02
• Study Start: 2018-01-02
• Last Update Posted: 5 February 2018

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 235

Inclusion Criteria

1. Women aged 23–65-years old
2. Diagnosed with ASC-US + HR-HPV, or LSIL + HR-HPV, or HSI

Exclusion Criteria

Diagnosed with cervical cancer.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Satisfaction with the notification manner regarding their test result is measured using the self-administrated questionnaire at week one<br>2. Health related quality of life is measured using the Functional Assessment of Chronic Illness Therapy-Cervical Dysplasia (FACIT-CD) and the Hospital Anxiety and Depression Scale (HADS) at week one

Secondary Outcome Measures

Name	Time	Method
There are no secondary outcome measures.