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Tailored Interactive Intervention to Increase CRCS

NCT01084746 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1224

Last updated 2018-05-11

No results posted yet for this study

Summary

The primary goal of this research project is to conduct a 5-year prospective randomized trial of a theory-based intervention to increase patient completion of colorectal cancer screening (CRCS) among patients ages 50 to 64 years old.

Conditions

  • Colorectal Cancer Screening

Interventions

BEHAVIORAL

PC-based tailored intervention

Patients will receive a tailored interactive PC-based intervention at a freestanding kiosk.

BEHAVIORAL

Printed educational materials

Patients will receive generic printed educational materials about CRCS in the PEC when they arrive at the Main Campus for their appointment.

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH

  • The University of Texas Health Science Center, Houston

    lead OTHER

Principal Investigators

  • Sally W Vernon, PhD · The University of Texas Health Science Center, Houston

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Max Age
64 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2005-01-31
Primary Completion
2008-06-30
Completion
2008-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01084746 on ClinicalTrials.gov