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Completed

NCT Number: NCT00351676

Capturing Outcomes of Clinical Activities Performed by a Rounding Pharmacist Practising in a Team Environment

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).

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Key information

About this study

The overall goal of the COLLABORATE study is to improve processes of care and patient outcomes by optimizing drug therapy via a hospital pharmacy practice model that integrates clinical pharmacists into the patient care team.

The intervention consists of a clinical pharmacist assigned to the patient care team for the purpose of providing proactive clinical pharmacy services. The study pharmacist will be available during normal office hours 5 days per week to provide clarification of the patient's medication history, identify and resolve actual and potential patient specific drug related problems/issues, participate in patient care rounds, provide drug information to the patient care team, provide patient education and discharge medication counselling, and provide physician and/or nursing staff education. The anticipated pharmacist to patient ratio is approximately 1:20.

Control patients will receive usual care. Usual care consists of reactive clinical pharmacy services (i.e. drug related issues identified as orders are received, or by patient profile review) provided by a ward based, not team based, clinical pharmacist.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • Residence outside the Capital Health catchment
  • Admitted for ≤ 2 days
  • Palliative care
  • Transferred to another team

Treatment and study plan

Integration of a team based clinical pharmacist

Behavioral

Optimizing therapeutic treatments

Drug

Optimizing processes of care

Behavioral

Primary outcomes

  1. Improvement in proportion of quality indicators achieved, for target diseases as a most responsible or primary diagnosis, between groups.

    Time frame: in hospital

Secondary outcomes

  1. Differences in condition-specific achievement of drug therapy quality indicators;

    Time frame: in hospital

  2. Differences in 6 month hospital readmission rate;

    Time frame: 6 months

  3. Differences in number, type, acceptance rate, and expected impact of all pharmacist interventions;

    Time frame: in hospital

  4. Qualitative evaluation of the impact of the intervention via interviews with the participating pharmacists and physicians.

    Time frame: in hospital

Sponsors and collaborators

Lead sponsor

University of Alberta

Other

Collaborators

  • Capital Health, Canada

Registry information

Official study title

Capturing Outcomes of Clinical Activities Performed by a Rounding Pharmacist Practising in a Team Environment (COLLABORATE)

Important dates

Study start
2006
Study completion
2007
First posted
Jul 13, 2006
Registry last updated
Dec 11, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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