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Human Papilloma Virus (HPV) Self swab for Human Papillomavirus
N/A
Recruiting
Led By Ann Chang, MD
Research Sponsored by University of Hawaii
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediately after swab is collected
Awards & highlights
Study Summary
In this study, the investigators will assess whether implementing a self-swab protocol for primary Human Papilloma Virus (HPV) testing is an effective method to increase cervical cancer screening in a sample of unscreened women in Hawaii. The findings of this study may support adoption of HPV self swab protocols both at Kalihi Palama Health Center (KPHC) and other Federally Qualified Health Centers (FQHC) in Hawaii.
Eligible Conditions
- Human Papillomavirus
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ immediately after swab is collected
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~immediately after swab is collected
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Percentage of participants with abnormal result
Percentage of swabs with result
Secondary outcome measures
Knowledge of HPV
Knowledge of cervical cancer
Self reported ease of collecting the swab
+2 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: Human Papilloma Virus (HPV) Self swabExperimental Treatment1 Intervention
Enrolled participants will be instructed to perform a self swab for genital Human Papilloma Virus (HPV) infection. Additionally, a short survey will be administered to collect demographic information, evaluate knowledge of HPV/cervical cancer, and assess acceptability of HPV self swab.
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Who is running the clinical trial?
University of HawaiiLead Sponsor
115 Previous Clinical Trials
54,605 Total Patients Enrolled
Ann Chang, MDPrincipal InvestigatorUniversity of Hawaii
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