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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02888782
Other study ID # HREB-2016.221
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date December 8, 2016
Est. completion date June 29, 2018

Study information

Verified date October 2018
Source Memorial University of Newfoundland
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients who are discharged from hospital can be overwhelmed when they suddenly have to manage new conditions or medications. These changes can be particularly difficult for people on many medications or with multiple health conditions. There is a real risk that this will lead to emergency room visits, hospital readmission, and even death. In addition to endangering patients, these adverse events are very costly to the healthcare system. The good news is that these events can be preventable if patients receive care that is better coordinated.

Patient-oriented research will be conducted to determine if a pharmacist-led medication therapy management service can improve health outcomes of 'medically complex' patients transitioning from acute to primary care in Newfoundland and Labrador (NL). This a more comprehensive service than their community pharmacist would normally provide. The program will use a new Pharmacist Clinic service to provide care and support which does not currently exist for patients in NL after they leave hospital. After discharge, patients will be randomly divided into two groups: one group will receive care as usual from their doctor; the other group will have their medications assessed by a clinic pharmacist within one week of hospital discharge along with their usual care from their doctor. The two groups will be compared to determine whether specialized pharmacist services after hospital discharge is satisfactory to patients/providers, improves patient health, and reduces emergency room visits, hospital readmissions, and repeat trips to the doctor. If successful, this project will help ensure that patients are taking the right medications in the right way, improving individual health and making better use of healthcare system resources.


Recruitment information / eligibility

Status Terminated
Enrollment 89
Est. completion date June 29, 2018
Est. primary completion date April 30, 2018
Accepts healthy volunteers No
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria:

1. 50 years of age or older

2. Admitted to a General Medicine ward

3. Take 5 or more chronic medications

Exclusion Criteria:

1. Discharge to a long term care facility

2. Life expectancy less than 3 months

3. Have entered palliative care

4. Cognitive impairment (unless a responsible caregiver can provide consent and assist in participation)

5. Non-English speaking

6. Unable to provide informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Pharmacist Consultation


Locations

Country Name City State
Canada Health Sciences Center Saint John's Newfoundland and Labrador
Canada St. Clares Mercy Hospital St. John's Newfoundland and Labrador

Sponsors (1)

Lead Sponsor Collaborator
Memorial University of Newfoundland

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Patient Satisfaction Survey Measured using a Likert scale questionnaire Collected 3 - 6 months after study enrollment
Other Pharmacist Satisfaction Survey Measured using a Likert scale questionnaire Collected at the end of study period (12-15 months)
Other Physician Satisfaction Survey Measured using a Likert scale questionnaire Collected at the end of study period (12-15 months)
Other Patient quality of life Short Form Health Survey Measured using a Short Form Health Survey (SF-36) Collected at time of hospital discharge
Other Patient quality of life Short Form Health Survey Measured using a Short Form Health Survey (SF-36) Collected at 30, 60 and 90 days post hospital discharge
Primary Composite Hospital Utilization Rate A composite score of hospital readmission rate and ER visits 30 days post discharge
Secondary Number of Emergency Room Visits 30 days post discharge
Secondary Number of Emergency Room Visits 60 days post discharge
Secondary Number of Emergency Room Visits 90 days post discharge
Secondary Rehospitalization Rate 30 days post discharge
Secondary Rehospitalization Rate 60 days post discharge
Secondary Rehospitalization Rate 90 days post discharge
Secondary Mortality Rate 30 days post discharge
Secondary Mortality Rate 60 days post discharge
Secondary Mortality Rate 90 days post discharge
Secondary Frequency of Family Physician Visits 30 days post discharge
Secondary Frequency of Family Physician Visits 60 days post discharge
Secondary Frequency of Family Physician Visits 90 days post discharge
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