CP4ACS - Delphi Study to Determine Appropriateness of STEMI Quality Indicators in Belgium
Sponsor
European Pathway Association (Other)
Overall Status
Completed
CT.gov ID
NCT02030210
Collaborator
Universitaire Ziekenhuizen Leuven (Other), KU Leuven (Other)
32
1
4
7.9
Study Details
Study Description
Brief Summary
RAND/UCLA modified Delphi study on quality indicators for STEMI to determine the appropriateness of quality indicators retrieved from literature and guideline review. We aim to engage 20 cardiologists and 20 nurses with relevant experience in the care for STEMI patients.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Study Type:
Observational
Actual Enrollment
:
32 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Quality of Care for STEMI - Patients. a Research to Determine Appropriateness of STEMI Quality Indicators in Belgium, a RAND/UCLA Modified Delphi Study
Study Start Date
:
Jul 1, 2013
Actual Primary Completion Date
:
Nov 1, 2013
Actual Study Completion Date
:
Nov 1, 2013
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
cardiologists
|
|
study coordinators
|
|
registred nurses
|
Outcome Measures
Primary Outcome Measures
- validated quality indicators for STEMI care in belgium (both on patient and on hospital level) [2 months]
33 experts in cardioloy, cardio nursing and quality rated quality indicators for STEMI care in belgian hospitals on a 9 point Likert Scale. All indicators with a median score between 7 and 9 were discussed in an expert panel. The expert panel selected validated quality inidicators for STEMI care.
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
to 99 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
- cardiologist or cardio nurse with relevant experience in the care for STEMI patients
Exclusion Criteria:
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | KU Leuven | Leuven | Vlaams Brabant | Belgium |
Sponsors and Collaborators
- European Pathway Association
- Universitaire Ziekenhuizen Leuven
- KU Leuven
Investigators
- Principal Investigator: Kris Vanhaecht, dr, KU Leuven
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Dr. Kris Vanhaecht,
Study director,
European Pathway Association
ClinicalTrials.gov Identifier:
NCT02030210
Other Study ID Numbers:
- CP4ACS\2013\1
First Posted:
Jan 8, 2014
Last Update Posted:
Apr 4, 2022
Last Verified:
Mar 1, 2022
Keywords provided by Dr. Kris Vanhaecht,
Study director,
European Pathway Association
Additional relevant MeSH terms: