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Spots Global Cancer Trial Database for Patient Activation Intervention in Improving Screening Rates for Colorectal Cancer

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Patient Activation Intervention in Improving Screening Rates for Colorectal Cancer

Official Title: Patient Activation To Increase Colon Cancer Screening (THE CHAT STUDY)

Study ID: NCT01801059

Study Description

Brief Summary: This randomized clinical trial focused on activating the patient to ask their health care provider for a colorectal cancer screening test to improve screening rates for colorectal cancer. The patient activation intervention may increase information seeking, number of screening tests ordered and number of completed screening tests for colorectal cancer.

Detailed Description: PRIMARY OBJECTIVES: I. To test a patient activation intervention to improve colorectal cancer (CRC) screening rates using fecal occult blood test (FOBT) among male and female patients 50 years and older from the East Central Columbus Neighborhood Health Center. SECONDARY OBJECTIVES: I. To assess if there is a change in knowledge and attitudes about CRC screening after watching the educational video. II. To assess the effectiveness of providing communication skills training for improving discussion focusing on CRC screening during the patient-provider visit. OUTLINE: Patients are randomized to 1 of 2 arms prior to a medical visit. ARM I (Education only): Patients receive CRC and CRC screening information by an educational video and a brochure with healthy hints to prevent CRC. ARM II (Education and patient activation): Patients receive CRC and CRC screening information and communication skills training (patient activation) intervention by educational video and brochure and a brochure about healthy hints to prevent CRC. After the medical visit, patients' medical records are reviewed at 1 month and 2 months after the visit to document CRC screening completion.

Eligibility

Minimum Age: 50 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: Yes

Locations

Arthur G. James Cancer Hospital and Solove Research Institute at Ohio State University Medical Center, Columbus, Ohio, United States

Contact Details

Name: Mira Katz

Affiliation: Ohio State University Comprehensive Cancer Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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