Implementation of Guidelines on Hereditary or Familial Colorectal Cancer

NCT00929097 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2009-06-26

No results posted yet for this study

Summary

The aim of this study is to improve clinicians' calculation, interpretation and communication of familial colorectal cancer risk, as well as patients' risk perception and uptake of referral for genetic counselling or for surveillance by colonoscopy for their relatives at risk.

Conditions

  • Colorectal Neoplasms, Hereditary Nonpolyposis

Interventions

OTHER

Implementation aids

* Patients and clinicians have access to a website with information on familial colorectal cancer risk; a risk assessment tool and decision aids * Clinicians receive the guidelines and a risk communication tool, as well as education

OTHER

Control

Dissemination of guidelines

Sponsors & Collaborators

  • Cardiff University

    collaborator OTHER
  • Erasmus Medical Center

    collaborator OTHER
  • Leiden University Medical Center

    collaborator OTHER
  • University Medical Center Groningen

    collaborator OTHER
  • Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

    collaborator OTHER
  • Comprehensive Cancer Centres

    collaborator UNKNOWN
  • ZonMw: The Netherlands Organisation for Health Research and Development

    lead OTHER

Principal Investigators

  • Nicoline Hoogerbrugge, MD, PhD · Radboud University Medical Center

  • Rosella PMG Hermens, PhD · Radboud University Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-10-31
Primary Completion
2011-07-31
Completion
2012-01-31

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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 NCT00929097 on ClinicalTrials.gov