RECRUITING

Expanding Access to Cervical Cancer Screening Through Primary HR-HPV Testing and Self-sampling: a Multicomponent Intervention for Safety Net Health Systems

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

To learn about the attitudes toward implementing self-collection among healthcare providers and staff, participants, and other stakeholders; and to inform the development of patient education and provider training materials to aid in the implementation of self-collection in clinical settings.

Official Title

Expanding Access to Cervical Cancer Screening Through Primary HR-HPV Testing and Self-sampling: a Multicomponent Intervention for Safety Net Health Systems

Quick Facts

Study Start:2025-02-17
Study Completion:2031-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06843720

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 65 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Currently a resident in the state of Texas
  2. * Attend for care at a partner clinic enrolled in the study
  3. * Women and persons with a cervix
  4. * Age 25-65
  5. * Due or past due for cervical cancer screening
  6. * Purposively identified as a stakeholder for formative research by research staff Investigators, clinic staff, and other health system stakeholders from partnering health systems:
  7. * Employed at least part-time by a partnering health system
  8. * Age 18+
  9. * Participate in at least one Project ECHO session
  10. * Age 18+
  1. * Report being currently pregnant
  2. * History of total hysterectomy
  3. * History of cervical cancer

Contacts and Locations

Study Contact

Jane R Montealegre, PHD
CONTACT
713- 745-5008
jrmontealegre@mdanderson.org

Study Locations (Sites)

MD Anderson Cancer Center
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: M.D. Anderson Cancer Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-02-17
Study Completion Date2031-03-31

Study Record Updates

Study Start Date2025-02-17
Study Completion Date2031-03-31

Terms related to this study

Additional Relevant MeSH Terms

  • HR-HPV Testing