Capturing Outcomes of Clinical Activities Performed by a Rounding Pharmacist Practising in a Team Environment
1 other identifier
interventional
452
1 country
3
Brief Summary
We, the researchers, propose to link a clinical pharmacist with an internal medicine or family medicine team to provide pharmaceutical care to all patients assigned to the team. The hypothesis is that through this team based approach, pharmacists will act as a resource for providing pharmacotherapeutic advice during the drug therapy decision making process and promote optimal drug use by identifying and resolving actual and potential drug related problems. This study is designed to test this hypothesis, by assessing the impact of this intervention on evidence based, quality of drug therapy indicators, for patients admitted with heart failure (HF), chronic obstructive pulmonary disease (COPD), community acquired pneumonia (CAP), type 2 diabetes mellitus (T2DM), and stable coronary artery disease (CAD).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_4
Started Feb 2006
3 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2006
CompletedFirst Submitted
Initial submission to the registry
July 12, 2006
CompletedFirst Posted
Study publicly available on registry
July 13, 2006
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2007
CompletedDecember 11, 2007
February 1, 2006
July 12, 2006
December 7, 2007
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Improvement in proportion of quality indicators achieved, for target diseases as a most responsible or primary diagnosis, between groups.
in hospital
Secondary Outcomes (4)
Differences in condition-specific achievement of drug therapy quality indicators;
in hospital
Differences in 6 month hospital readmission rate;
6 months
Differences in number, type, acceptance rate, and expected impact of all pharmacist interventions;
in hospital
Qualitative evaluation of the impact of the intervention via interviews with the participating pharmacists and physicians.
in hospital
Interventions
Eligibility Criteria
You may qualify if:
- Consecutive patients \> 18 years of age admitted to participating internal and family medicine teams during the 1 year study period will be eligible to receive the pharmacist intervention. For the purposes of data analysis, patients with a most responsible or primary diagnosis of HF, COPD, CAP, T2DM, and CAD will be included.
You may not qualify if:
- Residence outside the Capital Health catchment
- Admitted for ≤ 2 days
- Palliative care
- Transferred to another team
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Albertalead
- Capital Health, Canadacollaborator
Study Sites (3)
Royal Alexandra Hospital
Edmonton, Alberta, T5H 3V9, Canada
University of Alberta Hospital
Edmonton, Alberta, T6G 2B7, Canada
Grey Nuns Community Hospital
Edmonton, Alberta, T6L 5X8, Canada
Related Publications (2)
Makowsky MJ, Koshman SL, Midodzi WK, Tsuyuki RT. Capturing outcomes of clinical activities performed by a rounding pharmacist practicing in a team environment: the COLLABORATE study [NCT00351676]. Med Care. 2009 Jun;47(6):642-50. doi: 10.1097/MLR.0b013e3181926032.
PMID: 19433997DERIVEDMakowsky MJ, Schindel TJ, Rosenthal M, Campbell K, Tsuyuki RT, Madill HM. Collaboration between pharmacists, physicians and nurse practitioners: a qualitative investigation of working relationships in the inpatient medical setting. J Interprof Care. 2009 Mar;23(2):169-84. doi: 10.1080/13561820802602552.
PMID: 19234987DERIVED
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ross T. Tsuyuki, PharmD, MSc
University of Alberta
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
July 12, 2006
First Posted
July 13, 2006
Study Start
February 1, 2006
Study Completion
July 1, 2007
Last Updated
December 11, 2007
Record last verified: 2006-02