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

NCT ID: NCT01351441

Last Updated: 2020-06-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-05-31

Study Completion Date

2012-11-30

Brief Summary

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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.

Detailed Description

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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).

Conditions

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Medication Adherence Health Literacy Geriatric Patient Care Improvement Pharmacy Economic Improvement

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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Age 65 years or over AND at least 5 chronic medications

Group Type OTHER

Medication adherence consultation

Intervention Type BEHAVIORAL

Patients will be counseled in person on day 0 then telephonically every month after until day 365.

Medication problems assessment

Intervention Type OTHER

Patients will be asked if they are having any issues that may be attributable to their current drug therapy on a monthly basis. Any issue that is identified will be addressed by the pharmacist.

Beer's Criteria Assessment

Intervention Type OTHER

The patient's drug therapy will be reviewed for Beer's criteria medications and possible alternatives will be addressed by the pharmacist if deemed appropriate.

Health Literacy Assessment

Intervention Type BEHAVIORAL

Patients will be given a Health Literacy Assessment on day 0 and day 365 using the Realm-SF.

Interventions

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Medication adherence consultation

Patients will be counseled in person on day 0 then telephonically every month after until day 365.

Intervention Type BEHAVIORAL

Medication problems assessment

Patients will be asked if they are having any issues that may be attributable to their current drug therapy on a monthly basis. Any issue that is identified will be addressed by the pharmacist.

Intervention Type OTHER

Beer's Criteria Assessment

The patient's drug therapy will be reviewed for Beer's criteria medications and possible alternatives will be addressed by the pharmacist if deemed appropriate.

Intervention Type OTHER

Health Literacy Assessment

Patients will be given a Health Literacy Assessment on day 0 and day 365 using the Realm-SF.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Community Pharmacy Foundation

OTHER

Sponsor Role collaborator

VascuScript Pharmacy

OTHER

Sponsor Role lead

Responsible Party

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Scott V. Monte

Clinical Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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VascuScript Pharmacy

Cheektowaga, New York, United States

Site Status

Countries

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United States

Other Identifiers

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PHP1140411E

Identifier Type: -

Identifier Source: org_study_id

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