Evaluating Tools for Health Promotion and Disease Prevention

NCT00164658 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 8400

Last updated 2010-01-07

No results posted yet for this study

Summary

The study will evaluate the effect of familial risk assessment and prevention prompts tailored to familial risk on health behaviors and use of preventive services among adults who are members of primary care practices in the U.S.

Conditions

Interventions

BEHAVIORAL

Familial risk assessment and personalized prevention messages

Sponsors & Collaborators

Principal Investigators

  • Louise S Acheson, MD, MS · Case Western Reserve University Department of Family Medicine & CWRU/UHC Comprehensive Cancer Center

  • Wendy S Rubinstein, MD, PhD · Evanston Northwestern Healthcare Research Institute

  • Suzanne M O'Neill, MA, MS, PhD · Evanston Northwestern Healthcare Research Institute

  • Mack T Ruffin IV, MD, MPH · University of Michigan

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
35 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2005-09-30
Completion
2007-10-31

Countries

  • United States

Study Locations

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Entities

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 NCT00164658 on ClinicalTrials.gov