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N/A N=48 Randomized Double-blind Screening

Multilevel Intervention Based on Colorectal Cancer (CRC) and Cervical Cancer Self-screening in Rural, Segregated Areas

Colorectal Cancer Screening · Cervical Cancer Screening

Enrolled (actual)
48
Serious AEs
0.0%
Results posted
Oct 2022
Primary outcome: Primary: Difference in Percentage of Participants Who Completed Any Cervical PLUS Colorectal Cancer Screening Tests — 18; 1 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Self-sampling HPV test (Diagnostic_test); Fecal occult blood test (Diagnostic_test)
Age
Adult, Older Adult · 50+ yrs
Sex
Female
Sponsor
Milton S. Hershey Medical Center
Primary completion
Mar 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Difference in Percentage of Participants Who Completed Any Cervical PLUS Colorectal Cancer Screening Tests
18; 1
SECONDARY
Difference in Percentage of Participants Who Completed At-home Cervical PLUS Colorectal Cancer Screening Tests
17; 0

Summary

In this study, the investigators will deliver self-sampling human papillomavirus (HPV) tests and fecal immunochemical test (FIT) kits, as well as adapted cancer screening educational materials, by mail to 110 women who are out-of-date for both cervical and colorectal cancer screenings, recruited through federally qualified health centers (FQHCs) in rural, segregated counties of Pennsylvania. The hypothesis is that delivering self-sampling HPV tests and FIT, as well as adapted educational materials, to women in rural, segregated areas could help increase cancer screening, reduce geographic cancer disparities, and improve public health.

Eligibility Criteria

Inclusion Criteria

  • lives in rural, segregated county of Pennsylvania
  • able to speak, read, and communicate well in English
  • out of date for both cervical and colorectal cancer screening

Exclusion Criteria

  • has had a partial or complete hysterectomy
  • has a family history of colorectal cancer
  • has a personal history of cervical or colorectal cancer
  • persons who are cognitively impaired
  • persons who are incarcerated
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04471194). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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