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Integrated Care for Cancer Patients; Developing, Implementing and Testing a Programme to Improve Integrated Care

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified February 2007 by Radboud University.
Recruitment status was:  Recruiting
Information provided by:
Radboud University Identifier:
First received: August 25, 2005
Last updated: February 28, 2007
Last verified: February 2007

The purpose of this study is to compose, implement and evaluate a programme to improve the quality of integrated care for patients with cancer.

Literature will be searched for components of integrated care programmes. On the basis of evidence based multi-disciplinary guidelines and literature on integrated care programmes, a set of indicators will be composed. This set will be measured in 6 hospitals on patients with non-small-cell-lung cancer. In two hospitals, an integrated care programme will be implemented and effects on processes and outcomes of care will be measured.

Condition Intervention
Neoplasms Behavioral: professional audit and feedback Behavioral: integrated care programmes

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Educational/Counseling/Training
Official Title: Integrated Care for Cancer Patients

Further study details as provided by Radboud University:

Primary Outcome Measures:
  • guideline adherence

Secondary Outcome Measures:
  • hospitalization
  • satisfaction
  • quality of life

Estimated Enrollment: 300
Study Start Date: August 2004
Estimated Study Completion Date: July 2007

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Each new patient that visits the lung specialist in 6 hospitals in the east part of Holland, in the period from September 2004 till March 2005

Exclusion Criteria:

  • Mortality
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00135980

Contact: Marielle Ouwens, MSc +31243613114
Contact: Rosella Hermens, MSc,PhD +31243613129

Rijnstate Hospital Recruiting
Arnhem, Netherlands
Contact: Hans Smit, MD   
Principal Investigator: Marielle Ouwens, MSc         
MaasHospital Pantein Recruiting
Boxmeer, Netherlands
Contact: René Bunnik, MD   
Principal Investigator: Marielle Ouwens, MsC         
Slingeland Hosptital Recruiting
Doetinchem, Netherlands
Contact: Gerrit Bosman, MD   
Principal Investigator: Marielle Ouwens, MSc         
Gelderse Vallei Hospital Recruiting
Ede, Netherlands
Contact: Marietje Oudijk, MD   
Principal Investigator: Marielle Ouwens, MSc         
CWZ Hospital Recruiting
Nijmegen, Netherlands
Contact: René Termeer, MD   
Principal Investigator: Marielle Ouwens, MSc         
Radboud University Medical Centre Recruiting
Nijmegen, Netherlands
Contact: Miep vanderDrift, MD   
Principal Investigator: Marielle Ouwens, MSc         
Sponsors and Collaborators
Radboud University
Principal Investigator: Rosella Hermens, MSc,PhD Centre for Quality of Care Research, Radboud University Nijmegen Medical Centre
Study Director: Hub Wollersheim, MD,PhD Centre for Quality of Care Research, Radboud University Medical Centre
  More Information

Publications: Identifier: NCT00135980     History of Changes
Other Study ID Numbers: PACT-study M2100
Study First Received: August 25, 2005
Last Updated: February 28, 2007 processed this record on August 18, 2017