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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02937545
Other study ID # Pro00068552
Secondary ID 2R01GM081416-08A
Status Completed
Phase N/A
First received
Last updated
Start date February 22, 2017
Est. completion date September 10, 2019

Study information

Verified date May 2021
Source Duke University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to compare patient use of and satisfaction with community pharmacist-delivered pharmacogenetic (PGx) testing delivered along or as part of a medication therapy management (MTM) service. Pharmacist and patient outcome measures will be collected by surveys, interviews, and review of pharmacy records.


Description:

This study aims to investigate the delivery of pharmacogenetic (PGx) testing alone or in combination with Medication Therapy Management (MTM) in the community pharmacy setting in order to assess and compare the two delivery models. Using a clust randomized trial, these effects of these two models will be compared. Pharmacist and patient outcome measures will be collected by survey, interviews, and review of pharmacy records. The investigators intend to compare the effect of PGx alone and PGx with MTM from the pharmacy perspective (to assess impact on workflow/operations) and patient perspective (to assess acceptance of testing, understanding of results, medication adherence, and overall satisfaction with delivery model). In the PGx only arm, pharmacists will offer PGx testing to patients who are prescribed one of the 10 eligible drugs (aripiprazole, carisoprodol, celecoxib, citalopram, clopidogrel, metoprolol, nortriptyline, paroxetine, simvastatin, warfarin) and will return results to the patient and physician with any recommendations for drug or dosage changes based on results. In the PGx and MTM arm, pharmacists will offer PGx testing to patients prescribed one of the 10 eligible drugs and provide two MTM sessions: one at the time of testing, and one when results are returned. All patients will be surveyed before PGx testing and 3 months after receiving results. Pharmacists will be surveyed prior to their participation and following the conclusion of the study. Pharmacists will also conduct a chart review of patients and document all interactions with enrolled patients and their providers.


Recruitment information / eligibility

Status Completed
Enrollment 190
Est. completion date September 10, 2019
Est. primary completion date September 10, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Pharmacist participants must be community pharmacists licensed and practicing in North Carolina - Patient participants must be prescribed one of the 10 eligible medications (aripiprazole, carisoprodol, celecoxib, citalopram, clopidogrel, metoprolol, nortriptyline, paroxetine, simvastatin, warfarin) - Patient participants must be able to consent to participating and testing on their own, and be able to read English Exclusion Criteria: - Patients who have previously undergone pharmacogenetic testing will not be eligible.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Medication Therapy Management
Community pharmacists will provide medication therapy management in combination with pharmacogenetic testing
Pharmacogenetic testing
Community pharmacist will provide pharmacogenetic testing.

Locations

Country Name City State
United States Duke University Durham North Carolina

Sponsors (2)

Lead Sponsor Collaborator
Duke University National Institute of General Medical Sciences (NIGMS)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Patient Participants' Acceptance of PGx Services Offered in Community Pharmacy Setting Post-Study Survey question: "Now that you know your test results, would you have taken the test in the first place?" (Response: 'would definitely' have taken the test) Post-study Survey (after test results received)
Primary Number of Patient Participants Who Recalled All Test Results Post-Study Survey Question: "As best you can, please choose the result of your drug response test for the following genes" (Response: Result selected for all 5 genes) Post-study (after test results received)
Primary Number of Patient Participants Who Considered Time With Pharmacist to be Worthwhile Patient survey question - "Did you feel your time spent with the pharmacist was worthwhile?". Reported as number of participants who selected answer choice "Yes, definitely". Post-study (after test results received)
Primary Number of Patient Participants' With High Medication Adherence Pre-study (baseline) survey question: "In the last 7 days, I took all doses as prescribed" (Response: "strongly agree") Baseline (prior to testing)
Primary Number of Patient Participants With High Medication Adherence (Post-study) Post-study (follow-up) survey question: "In the last 7 days, I took all doses as prescribed" (Response: "strongly agree") Post-Study (after test results received)
Primary Number of Patient Participants Who Reported Understanding of Implications of Test Results Post_Study Survey Question: Please indicate your level of agreement with the following statement: "I understood clearly my choices for prevention or early detection of side effects." (Response: "Sometimes/Often") Post-study (after test results received)
Secondary Number of Pharmacist Participants Who Reported Strong Likelihood to Continue to Deliver PGx Testing Pharmacist Post-Survey Question: How likely are you to continue providing PGx testing in your pharmacy after the conclusion of the study? (Answer response: "definitely continue") Post-study (3 months)
Secondary Average Score of PGx Knowledge Assessment by Pharmacist Participants 7-question knowledge assessment of pharmacogenetics. Possible Score Range 0-7; actual range 3-7 (higher scores correspond to higher number of correct answers/higher knowledge) Baseline (prior to start of study)
Secondary Number of Pharmacist Participants Who Reported 'Reimbursement' as Most Common Barrier to Delivery of PGx Testing Pharmacist Post-Survey Question: Of the following potential barriers to providing PGx testing services, please indicate the greatest perceived barrier (most common response: "reimbursement") Post-study (3 months)
Secondary Number of Participating Pharmacists Who Feel Qualified to Deliver PGx Testing Pharmacist Post-Study survey question: I feel qualified to provide PGx testing at my pharmacy (Answer response: "strongly agree/agree"). Post-study (3 months)
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