← Back to Search

Receive routine instructions for Gynecologic Cancers

N/A
Waitlist Available
Led By Amanda Bruegl, MD
Research Sponsored by OHSU Knight Cancer Institute
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 post-intervention: 2 weeks after receipt of test results
Awards & highlights

Study Summary

This trial will compare whether it's better to get a cervical cancer screening via telehealth or mail, based on HPV sample collection, comfort with self-collection, and self-collection completion rates.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~post-intervention: 2 weeks after receipt of test results
This trial's timeline: 3 weeks for screening, Varies for treatment, and post-intervention: 2 weeks after receipt of test results for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Proportion of participants preferring self-collection to provider collection
Secondary outcome measures
Median discomfort level with self-collection
Median perceived difficulty understanding self-collection instructions

Trial Design

2Treatment groups
Active Control
Group I: Receive routine instructionsActive Control1 Intervention
Participants will receive routine instructions included in the myLAB Box Clinical Laboratory Improvement Amendments (CLIA) certified collection kit
Group II: Telehealth VisitActive Control1 Intervention
Participants will have a telehealth-based instructional visit and receive routine instructions included in the myLAB Box commercially available, CLIA certified collection kit

Find a Location

Who is running the clinical trial?

Oregon Health and Science UniversityOTHER
973 Previous Clinical Trials
6,845,898 Total Patients Enrolled
OHSU Knight Cancer InstituteLead Sponsor
230 Previous Clinical Trials
2,090,595 Total Patients Enrolled
1 Trials studying Gynecologic Cancers
28 Patients Enrolled for Gynecologic Cancers
Robert Wood Johnson FoundationOTHER
157 Previous Clinical Trials
686,703 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is my eligibility for participation in this medical research study confirmed?

"For this clinical trial, investigators are in search of 120 individuals between the ages 25-85 who possess gynecologic cancers. In addition to meeting these criteria, potential participants should either be pregnant (without poses any risk) or meet national cervical cancer screening guidelines for primary HPV testing (age 25 and older)."

Answered by AI

Are participants of all ages being admitted to this research endeavor?

"The conditions for entry into this clinical trial are that the patient must be aged between 25 and 85. There exists a separate study cohort made up of those below 18, while there is an additional sample group composed of those above 65 years old."

Answered by AI

How many volunteers are being admitted to this clinical experiment?

"Affirmative. According to the details on clinicaltrials.gov, this medical research program is still recruiting patients since it was initially published in January 19th 2022 and last updated on May 27th 2022. The study requires 120 participants across 2 different sites."

Answered by AI

Are there currently any opportunities for enrollment in this experimental program?

"Affirmative. The information on clinicaltrials.gov reveals that the study, which was initially published on January 19th 2022, is presently searching for participants. It needs to recruit 120 patients from 2 separate medical sites."

Answered by AI

Who else is applying?

What state do they live in?
Oregon
How old are they?
18 - 65
What portion of applicants met pre-screening criteria?
Met criteria
~40 spots leftby Apr 2025