RecruitingNot ApplicableNCT06498661

Self-collection for HPV Testing to Improve Cervical Cancer Prevention (SHIP) Trial (LMI-001-A-S01)

NCI Cervical Cancer 'Last Mile' Initiative 'Self-Collection for HPV Testing to Improve Cervical Cancer Prevention' (SHIP) Trial LMI-001-A-S01


Sponsor

National Cancer Institute (NCI)

Enrollment

750 participants

Start Date

Jun 26, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This clinical trial evaluates the use of self-collected vaginal samples for human papillomavirus (HPV) testing in patients referred for a colposcopy and/or cervical excisional procedures to improve cervical cancer prevention. HPV is a common virus which usually causes infections that last only a few months, but sometimes can last longer. It is known to cause a variety of cancers including cancer of the cervix. Even though there are ways to detect cervical cancer early, many individuals do not undergo screening that involves pelvic exams. Over half of all new cervical cancer cases are among those who have either never been screened or who are not screened enough. Without appropriate screening and care, preventable pre-cancers may turn into cancer. A new way to detect cervical cancer is to have individuals collect their own vaginal sample for HPV testing to know their risk for cervical cancer. This may give individuals more flexibility and comfort having the ability to collect samples themselves, compared to a doctor performing a speculum examination and collecting the samples in a clinic. This study compares clinical accuracy of HPV testing on self-collected vaginal samples versus cervical samples collected by clinician. The Self-collection for HPV Testing to Improve Cervical Cancer Prevention (SHIP) Trial is part of the National Cancer Institute (NCI)'s Cervical Cancer 'Last Mile' Initiative, a public private partnership that seeks to increase access to cervical cancer screening. The SHIP Trial focuses on developing clinical evidence to inform the US Food and Drug Administration (FDA)'s regulatory reviews of self-collection approaches as alternative sample collection approaches for cervical cancer screening. Several industry partner-specific self-collection device and assay combinations will be non-competitively and independently evaluated with a similar study design framework to inform pre-approval and/or post-approval regulatory requirements.


Eligibility

Sex: FEMALEMin Age: 25 Years

Plain Language Summary

Simplified for easier understanding

This study (called SHIP) is comparing self-collected vaginal swab HPV tests to standard cervical samples collected by a clinician, to see if women can test themselves for HPV and get equally accurate results for cervical cancer screening. **You may be eligible if...** - You are 25 or older with an intact cervix - You have been referred for colposcopy (a detailed cervical exam) due to a positive HPV test or abnormal Pap smear in the past 12 months - You are willing and able to undergo colposcopy and, if needed, a biopsy or treatment procedure **You may NOT be eligible if...** - You have had a hysterectomy (removal of the cervix) - You are unable to provide informed consent - You do not meet the referral criteria for colposcopy Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREBiospecimen Collection

Undergo collection of cervical samples by clinician

PROCEDURECervical Biopsy

Undergo cervical biopsy conducted by clinician

PROCEDUREColposcopy

Undergo colposcopy conducted by clinician

OTHERElectronic Health Record Review

Ancillary studies

PROCEDUREEndocervical Curettage

Undergo endocervical curettage conducted by clinician

PROCEDUREExcision

Undergo cervical excisional procedure conducted by clinician

PROCEDUREHPV Self-Collection

Undertake self-collection of vaginal samples

PROCEDUREHuman Papillomavirus Test

Undergo HPV testing of self-collected vaginal samples and cervical samples

OTHERQuestionnaire Administration

Ancillary studies

OTHERSurvey Administration

Ancillary studies


Locations(15)

University of Alabama at Birmingham Cancer Center

Birmingham, Alabama, United States

University of Miami Miller School of Medicine-Sylvester Cancer Center

Miami, Florida, United States

Emory University Hospital/Winship Cancer Institute

Atlanta, Georgia, United States

Louisiana State University Health Science Center

New Orleans, Louisiana, United States

Johns Hopkins University/Sidney Kimmel Cancer Center

Baltimore, Maryland, United States

University of New Mexico Cancer Center

Albuquerque, New Mexico, United States

Montefiore Medical Center-Einstein Campus

The Bronx, New York, United States

UNC Lineberger Comprehensive Cancer Center

Chapel Hill, North Carolina, United States

University of Cincinnati Cancer Center-UC Medical Center

Cincinnati, Ohio, United States

University of Oklahoma Health Sciences Center

Oklahoma City, Oklahoma, United States

University of Pennsylvania/Abramson Cancer Center

Philadelphia, Pennsylvania, United States

UPMC-Magee Womens Hospital

Pittsburgh, Pennsylvania, United States

M D Anderson Cancer Center

Houston, Texas, United States

VCU Massey Comprehensive Cancer Center

Richmond, Virginia, United States

University of Puerto Rico

San Juan, Puerto Rico

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