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Minimizing Risk and Maximizing Outcomes in Geriatric Patients Through Integrated Clinical Pharmacy Services in an Innovative Model of Community Practice

V

VascuScript Pharmacy

Status

Completed

Conditions

Medication Adherence
Pharmacy Economic Improvement
Geriatric Patient Care Improvement
Health Literacy

Treatments

Behavioral: Health Literacy Assessment
Behavioral: Medication adherence consultation
Other: Medication problems assessment
Other: Beer's Criteria Assessment

Study type

Interventional

Funder types

Other

Identifiers

NCT01351441
PHP1140411E

Details and patient eligibility

About

It has been shown that patients can improve their safety through informed choice, safe medication use, and complication reporting. This includes not only the potential problems that occur from prescription medication use but also issues that may arise through the improper use of over-the-counter medications. The willingness of a patient to take on safety action is known to be complicated by an unwillingness to behave in a manner that might challenge a physician's judgment or actions. Community pharmacists are in the unique position to provide perspective on the physician's recommendation and act as an advocate to facilitate necessary change. Through supportive and repeated interaction with their community pharmacist patients will develop assertiveness toward their own health care, an increased frequency and quality of interaction with their physician, and thus a minimized risk of harm and maximized opportunity to optimize clinical outcomes.

Full description

This is a single center, observational study to determine if geriatric patients who are on five or more chronic medications will have a difference in clinical, humanistic, and/or economic outcome through an integrated clinical pharmacy service intervention. The primary efficacy objective will be assessed through a single cohort, paired research design measuring the change from baseline in the adherence rate, number of medication related problems, and Beers criteria medications. The primary economic objective will be assessed through prescription revenue to validate the employment of a 0.5-1.0 Full-time equivalent (FTE). Secondary efficacy objectives will be assessed through a single cohort, paired research design measuring the change from baseline in the health literacy, optimization in the anthropometrics, and health related quality of life (HRQOL).

Enrollment

20 patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients who are at least 65 years of age
  • Have at least 5 medications that they take on a chronic basis
  • Willing to have their prescriptions filled by VascuScript Pharmacy
  • Understand the terms of the informed consent

Exclusion criteria

  • Any patient who does not meet the requirements of the Inclusion Criteria

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Age 65 years or over AND at least 5 chronic medications
Other group
Treatment:
Behavioral: Health Literacy Assessment
Other: Beer's Criteria Assessment
Other: Medication problems assessment
Behavioral: Medication adherence consultation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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