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OpenTrials
Completed

NCT Number: NCT02748148

Implementation Study of Enhanced Medication Therapy Management in Primary Care Practice

The purpose of this study is to identify challenges and successes associated with implementing an enhanced medication therapy management service in primary care practice.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Elmwood Family Physicians

Marlton, New Jersey, 08053, United States

About this study

The specific aim of this study is to implement a Medication Therapy Management (MTM) service in primary care that is enhanced by the incorporation of pharmacogenomics (PGx) and medication risk mitigation (MRM) factor technology and is standardized by a systematic approach to evidence- and personalized-based medicine. The primary objective is to implement the systematic approach to delivering an enhanced MTM service in a primary care setting. Secondary objectives include: determine how successful the communication between prescriber and pharmacist is within implementing the service, determine how PGx testing can be incorporated into primary care prescribers' daily work flow, determine if patients are receptive to PGx testing, determine how satisfied prescribers are with an enhanced MTM clinical service and their confidence to conduct on their own, and determine if enhanced MTM optimizes or changes drug therapy for patients.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Receiving primary health care from Elmwood Family Physicians; and
  • Medicare beneficiary; and
  • Currently prescribed at least 7 medications, or prescriber feels patient would benefit from enhanced medication therapy management, or actual or suspected medication-related problem

Exclusion criteria

  • Not willing to participate in the study and sign informed consent; or
  • Non-English speaking or designated surrogate as translator not available

Treatment and study plan

Medication therapy management

Other

Implementation of a systematic approach to evidence- and personalized-based medicine through a pharmacist-guided medication therapy management service

Other names: Enhanced medication therapy management

Primary outcomes

  1. Qualitative description of process-related challenges and successes as assessed by observation and survey

    Time frame: 3 months

    Implementation

Secondary outcomes

  1. Quantitative description of bidirectional communication as assessed by turn-around times from pharmacist's recommendations delivered to prescriber's responses received

    Time frame: 3 months

    Communication

  2. Qualitative description of incorporation of pharmacogenomic testing into workflow and receptiveness as assessed by observation and survey

    Time frame: 3 months

    Pharmacogenomic testing

  3. Qualitative description of prescriber satisfaction with enhanced medication therapy management services as assessed by survey

    Time frame: 3 months

    Prescriber survey

  4. Qualitative and quantitative description of potential impact of enhanced medication therapy management services on drug regimens as assessed by before-and-after observations

    Time frame: 3 months

    Impact

Sponsors and collaborators

Lead sponsor

Tabula Rasa HealthCare

Industry

Registry information

Official study title

Implementing an Enhanced Standardized Medication Therapy Management Approach Within a Primary Care Setting

Acronym: EMTM

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Apr 22, 2016
Registry last updated
Oct 17, 2016

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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