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Implementation of a New Strategy to Identify HNPCC Patients

Cost Effectiveness of Two Different Implementation Procedures to Change Clinicians Practice Roles in the Detection of Hereditary Colorectal Cancer

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00141466
Enrollment
360
Registered
2005-09-01
Start date
2005-09-30
Completion date
2007-07-31
Last updated
2008-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Neoplasms, Hereditary Nonpolyposis Colorectal Cancer

Keywords

Hereditary colorectal cancer, Microsatellite instability, Physician roles, Health care implementation, Intervention

Brief summary

The purpose of this study is to compare two different strategies to implement a new method to identify patients with HNPCC, which appeared cost-effective and feasible. The effectiveness, costs and feasibility of both of the implementation strategies will be assessed.

Detailed description

The Radboud University Nijmegen Medical Centre developed a new method to identify patients with HNPCC. This method appeared cost-effective and feasible. Using this new method 70% of the HNPCC patients will be identified as compared to less than 30% when the current method is used. However, this new method does not implement itself; large gaps exists between best evidence and daily practice. This study will compare an intensive strategy, consisting of distribution of educational materials, education, feedback and reminders, with a minimal strategy, only consisting of distribution of a critical care pathway. The aim is to find the most cost-effective strategy to implement the new method to identify patients with HNPCC in the Netherlands.

Interventions

BEHAVIORALEducation for professionals
BEHAVIORALDistribution of educational materials
BEHAVIORALFeedback for professionals
BEHAVIORALReminders for professionals

Sponsors

ZonMw: The Netherlands Organisation for Health Research and Development
CollaboratorOTHER
Radboud University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Colorectal cancer before the age of 50 years * Second colorectal cancer at any age * Colorectal cancer and other HNPCC associated extracolonic cancer irrespective of age at diagnosis * Adenoma with high grade dysplasia diagnosed before the age of 40 years

Design outcomes

Primary

MeasureTime frame
Efficacy of inclusion of eligible CRC-patients for MSI testing by pathologists.
Efficacy of referral of patients who are MSI positive to a clinical geneticist by surgeons.

Secondary

MeasureTime frame
Experiences with and acceptance of changed physician practice roles by patients and clinicians.
Cost efficacy of the implementation procedures.

Countries

Netherlands

Contacts

Primary ContactLucy I Overbeek, MSc
l.overbeek@antrg.umcn.nl+31-24-3613946
Backup ContactNicoline Hoogerbrugge, MD PhD
n.hoogerbrugge@antrg.umcn.nl+31-24-3613946

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026