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Clinical Trials/NCT00387998
NCT00387998
Completed
N/A

Randomized Trial of a Primer to Help Patients Understand Risk

Dartmouth-Hitchcock Medical Center0 sites555 target enrollmentOctober 2004

Overview

Phase
N/A
Intervention
Not specified
Conditions
Unspecified Adult Solid Tumor, Protocol Specific
Sponsor
Dartmouth-Hitchcock Medical Center
Enrollment
555
Primary Endpoint
Ability to interpret medical statistics as measured by a medical data interpretation test
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

RATIONALE: Understanding the risk of disease and prevention and screening activities to lower disease risk may help individuals make informed medical decisions.

PURPOSE: This randomized clinical trial is studying how well health education materials help participants understand medical information.

Detailed Description

OBJECTIVES: * Compare medical data interpretation skills in participants of low or high socioeconomic status who receive a general education primer (entitled "Know Your Chances: Understanding Health Statistics") vs a health education booklet (entitled "The Pocket Guide to Good Heath for Adults"). OUTLINE: This is a randomized, controlled study. Participants are stratified according to socioeconomic status (low vs high). Participants are randomized to 1 of 2 intervention arms. * Arm I (control): Participants receive a health education booklet entitled "The Pocket Guide to Good Health for Adults," published by the Agency for Health Care Research and Quality, which contains general information about disease risk and reducing risk by following recommended prevention or screening activities. * Arm II (primer): Participants receive a general education primer entitled "Know your chances: Understanding health statistics," which teaches how to understand disease risk and the benefits and risks of intervention. Within 2 weeks after receiving the education material, participants in both arms complete a survey, including a medical data interpretation test, STAT-interest, STAT-confidence, and user ratings of the education materials. PROJECTED ACCRUAL: A total of 555 participants were accrued for this study.

Registry
clinicaltrials.gov
Start Date
October 2004
End Date
August 2005
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Ability to interpret medical statistics as measured by a medical data interpretation test

Time Frame: 2 weeks

medical data interpretation skills

Secondary Outcomes

  • Interest in interpreting medical statistics, as measured by STAT-interest(2 weeks)
  • Confidence in interpreting medical statistics, measured by STAT-confidence(2 weeks)
  • User ratings of materials(2 weeks)

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