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NCT00148226 Clinical Trial

ICIBS Trial - Improving Patient Information About Bowel Cancer Screening - a Decision Aid Trial

Colorectal Cancer Screening Clinical Trial

Official title:
Randomized Controlled Trial of Patient Decision Aids for Faecal Occult Blood Test Screening

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00148226
Other study ID # 211205
Secondary ID
Status Completed
Phase Phase 2
First received September 5, 2005
Last updated January 3, 2006
Start date November 2003
Est. completion date September 2005

Study information
Verified date September 2005
Source University of Sydney
Contact n/a
Is FDA regulated No
Health authority Australia: National Health and Medical Research Council
Study type Interventional

Clinical Trial Summary

This project has been completed and consisted of a randomised trial of six tailored decision aids giving patients evidence-based information about faecal occult blood test screening for bowel cancer. 314 Australians aged between 50-74 years were recruited from five general practices and randomised to received either the tailored decision aid with age-gender and family history specific information and values clarification exercise or a standard government information sheet.

The decision aid significantly increased the proportion of people who were informed participants in the screening program.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date September 2005
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 50 Years to 74 Years
Eligibility Inclusion Criteria:

- People aged 50-74 years who were eligible for FOBT screening under current Australian guidelines and had not had screening for colorectal cancer in the preceding two years

Exclusion Criteria:

- Poor English, impaired cognition, significant comorbidity

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Educational/Counseling/Training

Related Conditions & MeSH terms

Intervention

Behavioral:
• Decision Aid

Locations
Country Name City State
Australia University of Sydney Sydney New South Wales

Sponsors (1)
Lead Sponsor Collaborator
University of Sydney

Country where clinical trial is conducted

Australia, 

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