Point Of Care Testing In Danish General Practice - Part II (POCIP)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified June 2010 by Research Unit Of General Practice, Copenhagen.
Recruitment status was  Recruiting
Sponsor:
Collaborators:
Section of General Practice, Department of Public Health, Faculty of Health Sciences, University of Copenhagen
The Copenhagen General Practice Laboratorium
Centre for Quality Development and CME for GP's in the Capital Region
Region Capital Denmark
Information provided by:
Research Unit Of General Practice, Copenhagen
ClinicalTrials.gov Identifier:
NCT01152177
First received: June 23, 2010
Last updated: February 7, 2011
Last verified: June 2010
  Purpose

The aim of this project is to evaluate the efficacy of electronic reminder letters versus none on general practices adherence to clinical quality guidelines regarding Point Of Care Testing (POCT). The investigators hypothesize, that electronic reminder letters may increase adherence.


Condition Intervention
Point of Care Testing
Device: Electronic reminder letters
Device: Usual care

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Health Services Research
Official Title: Point-Of-Care Testing In Danish General Practice: A Randomised Controlled Trial - Part II

Further study details as provided by Research Unit Of General Practice, Copenhagen:

Primary Outcome Measures:
  • Total number of split tests performed in study period (three periods). [ Time Frame: January - April 2011 ] [ Designated as safety issue: No ]
    Total number of split tests performed in study period (three periods).


Secondary Outcome Measures:
  • Proportion of practices with a high quality of tests defined as 75% of the performed split tests for INR within the accepted interval according to the CGPL quality guidelines1 in study period. [ Time Frame: January - April 2011 ] [ Designated as safety issue: No ]
    Proportion of practices with a high quality of tests defined as 75% of the performed split tests for INR within the accepted interval according to the CGPL quality guidelines1 in study period.

  • Proportion of practices conducting split tests in study period. [ Time Frame: January - April 2011 ] [ Designated as safety issue: No ]
    Proportion of practices conducting split tests in study period.


Estimated Enrollment: 320
Study Start Date: August 2010
Estimated Study Completion Date: May 2011
Estimated Primary Completion Date: May 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Electronic reminders
Electronic reminders
Device: Electronic reminder letters
Electronic reminder letters if adherence is not obtained (up to four)
Other Name: ELECTRONIC
No Intervention: Usual care
usual care
Device: Usual care
Usual care
Other Name: USUAL

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   30 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • All GPs using at least 5 POCT analysis (either 5 Haemoglobin or 5 glucose) during baseline period (january-april 2010)

Exclusion Criteria:

  • All GPs using at least 5 INR POCT analysis during baseline period (january-april 2010).
  • GPs stopping during study period.
  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 ClinicalTrials.gov identifier: NCT01152177

Contacts
Contact: Frans B Waldorff, PhD fransw@sund.ku.dk

Locations
Denmark
Research Unit of General Practice Recruiting
Copenhagen, Capital, Denmark, 1014
Contact: Frans B Waldorff, Ph.D.    +4535327171    fransw@sund.ku.dk   
Research Unit of General Practice Not yet recruiting
Copenhagen, Denmark, 1014
Contact: Frans B Waldorff, PhD       fransw@sund.ku.dk   
Principal Investigator: Frans B Waldorff, PhD         
Sponsors and Collaborators
Research Unit Of General Practice, Copenhagen
Section of General Practice, Department of Public Health, Faculty of Health Sciences, University of Copenhagen
The Copenhagen General Practice Laboratorium
Centre for Quality Development and CME for GP's in the Capital Region
Region Capital Denmark
Investigators
Principal Investigator: Frans B Waldorff, PhD Research Unit of General Practice
  More Information

No publications provided by Research Unit Of General Practice, Copenhagen

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: GP, Associate Research Professor Frans Boch Waldorff, The Research Unit for General Practice, Copenhagen, Denmark
ClinicalTrials.gov Identifier: NCT01152177     History of Changes
Other Study ID Numbers: GP009900012
Study First Received: June 23, 2010
Last Updated: February 7, 2011
Health Authority: Denmark: Danish Dataprotection Agency

Keywords provided by Research Unit Of General Practice, Copenhagen:
Heading Health Plan Implementation
General Practice
Point of care testing
education

ClinicalTrials.gov processed this record on July 24, 2014