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NCT04414306Completed

Screen to Save 2: Rural Cancer Screening Educational Intervention

Source: ClinicalTrials.gov · Last updated 2 Feb 2026

Brief summary (registry, in English)

The purpose of this study is to help the Dartmouth Cancer Center and the National Cancer Institute understand how to educate people about cancer screening.

Status (registry)
Completed
Study type
Interventional
Enrollment
205 (actual)
First submitted
1 Jun 2020
Start date
8 Oct 2020
Primary completion date
30 Nov 2023
Lead sponsor
Dartmouth-Hitchcock Medical Center
NCT number
NCT04414306

What you commit to

  • Study type: Interventional
  • Participants enrolled: 205
  • From 8 Oct 2020 to the primary completion date, 30 Nov 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Answered a colorectal cancer screening history question indicating that the participant has never received colorectal cancer screening OR does not know if he/she has received colorectal cancer screening previously OR
  • Answered a series of questions indicating that the participant received prior colorectal cancer screening but may be overdue for colorectal cancer screening based on the type of colorectal cancer screening last reported and screening guidelines for the frequency of re-screening.
    • Six-Month Follow-Up Survey Inclusion Criteria:
    • A participant will be eligible for inclusion in the six-month follow-up survey if the participant participated in the three-month-follow up survey and at that time reported that having:
  • A FIT/FOBT screening or Cologuard (stool) screening performed since the time of initial study participation, but having not received the results
  • An abnormal FIT/FOBT, or Cologuard (stool) screening since the time of initial study participation, but had not received a diagnostic colonoscopy
  • A colonoscopy since the time of initial study participation, but had not received the final results

Other illness

  • \- Cognitive impairment preventing participation in informed consent process

Other

  • Three-Month Follow-Up Survey Inclusion Criteria:
  • A participant will be eligible for inclusion in the three-month follow-up survey if the participant completed the pre-test, educational intervention, and post-test and at the time of initial participation:

Who the study is looking for

  • Resident of one of the RUCC 7-9 counties in New Hampshire or Vermont (Coos or Sullivan County, NH; Caledonia, Windsor, Windham, Orange, Orleans, Lamoille, or Essex County, VT) and
  • Age 45-74 at the time of enrollment in the study

Age in the registry: 45 years to 75 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Dartmouth Cancer Center
Coordinator of this site? Confirm its status
LebanonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.