ClinicalTrials.gg
Status unknownNCT04971902Updated Sep 2, 2022

Pharmacist-led Pharmacogenomic Clinical Service Within the Program of All-inclusive Care for the Elderly

An observational study in Pharmacogenetic Testing, Elderly and Opioid Use, sponsored by Tabula Rasa HealthCare. Status unknown at 1 site in United States. Open to participants aged 55 Years and older. Per ClinicalTrials.gov, last updated 2022-09-02.

Sponsored by Tabula Rasa HealthCare · Observational

The sponsor has not verified this record recently (last verified Sep 2022), so the status shown — last known as Enrolling by invitation — may be out of date.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
2,500
Ages
55 Years and older
Sex
All
01

Study summary

Pharmacist-led pharmacogenomics (PGx) clinical services and medication safety reviews are currently being offered to PACE organizations under the direction of licensed healthcare prescribers by CareKinesis d/b/a Tabula Rasa HealthCare. This project aims to include patients enrolled in PACE organizations with chronic pain and who are prescribed CYP2D6 activated opioids. PGx testing will be performed by contractual PGx vendor with TRHC. PGx results will be integrated into TRHC's proprietary Clinical Decision Support System (Medication Risk Mitigation™ Matrix, CareKinesis, Moorestown, NJ) that guides pharmacists to identify drug-drug interactions (DDIs), drug-gene interactions (DGIs), and drug-drug-gene interactions (DDGIs).16 Clinical pharmacists will translate PGx results combined with a comprehensive DDI review into actionable clinical decisions. Clinical pharmacists will provide medication therapy management recommendation to address medication problems to the PACE prescriber (physician). PACE prescribers will review the pharmacist's recommendation, and based on their clinical assessment, the prescriber will decide whether or not to implement the opioid therapy recommendation.

Read the detailed description

Tabula Rasa HealthCare (TRHC), doing business as CareKinesis, is the first national pharmacy that provides science-based medication risk identification and mitigation technologies and services. CareKinesis utilizes medication decision support tools and pharmacists certified in geriatrics to provide pharmacy services for various healthcare organizations including PACE organizations.

Program of All-inclusive Care for the Elderly (PACE) is a Medicare-Medicaid program that provides comprehensive medical and supportive services to individuals >55 years of age who are certified by their state as needing nursing home care. As an alternative to institutionalization, PACE helps these individuals live safely in their community. The aim of PACE is to improve overall quality of life in four domains (physical, psychological, social, and spiritual) using a multidisciplinary approach. In the United States, the vast majority of PACE organizations collaborate with one pharmacy to dispense drugs, in addition to other pharmacy services, for their population of participants.15 Presently, CareKinesis services more than 35 PACE organizations, including approximately 75 PACE sites, across the country. As a national PACE pharmacy provider since 2011, CareKinesis focuses on improving medication regimens to reduce medication-related risks while enhancing economic, clinical and humanistic outcomes.

Study Design Pharmacist-led pharmacogenomics (PGx) clinical services and medication safety reviews are currently being offered to PACE organizations under the direction of licensed healthcare prescribers by CareKinesis d/b/a Tabula Rasa HealthCare. This project aims to include patients enrolled in PACE organizations with chronic pain and who are prescribed CYP2D6 activated opioids. PGx testing will be performed by a contractual PGx vendor with TRHC. PGx results will be integrated into TRHC's proprietary Clinical Decision Support System (Medication Risk Mitigation™ Matrix, CareKinesis, Moorestown, NJ) that guides pharmacists to identify drug-drug interactions (DDIs), drug-gene interactions (DGIs), and drug-drug-gene interactions (DDGIs).16 Clinical pharmacists will translate PGx results combined with a comprehensive DDI review into actionable clinical decisions. Clinical pharmacists will provide medication therapy management recommendation to address medication problems to the PACE prescriber (physician). PACE prescribers will review the pharmacist's recommendation, and based on their clinical assessment, the prescriber will decide whether or not to implement the opioid therapy recommendation.

The measurement of health-related quality of life (QoL) and pain assessment using the EQ-5D survey, and numerical rating scale (NRS) for pain will be performed during the study by PACE prescribers or the PACE interdisciplinary team (IDT) as follows:

  • Health-related quality of life questionnaire (EQ-5D) will be performed at baseline and at the completion of the study (visits 1 and 3, respectively)
  • NRS for pain will be performed at baseline (before the PGx testing), 1-2 and 2-3 weeks after TRHC's pharmacist recommendations (visits 1, 2 and 3, respectively) All PACE patients will continue to receive usual medical care throughout the study. Changes to drug regimens will be at the discretion of the patients' PACE prescribers.
02

Conditions studied

  • Pharmacogenetic Testing
  • Elderly
  • Opioid Use
  • Pain
  • Pain, Acute
  • Pain, Chronic
03

In context

Pain

2,450 studies on the registry are indexed under Pain; 945 are open to participants now.

This study's planned enrollment of 2,500 is above the median of 100 across 301 observational studies indexed under Pain.

Browse Pain studies →

Lead sponsor

Tabula Rasa HealthCare is the lead sponsor of 14 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
55 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Program of All-inclusive Care for the Elderly (PACE) is a Medicare-Medicaid program that provides comprehensive medical and supportive services to individuals >55 years of age who are certified by their state as needing nursing home care. As an alternative to institutionalization, PACE helps these individuals live safely in their community

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Patient enrolled in a PACE organization during the implementation period; and,
  2. PACE organization contractually receiving pharmacy services from CareKinesis
  3. Patient prescribed a CYP2D6 activated opioid, namely codeine, hydrocodone, oxycodone and/or tramadol
  4. Patients with chronic non-cancer pain (CNCP)
  5. Patient's prescriber orders a PGx test based upon his/her determination that the patient could potentially benefit from PGx testing
  6. Patient is able to read, understand, and provide informed consent to participate

Exclusion criteria

Exclusion Criteria:

  1. Patient prescribed an opioid that is not metabolized by CYP2D6 including, but not limited to, oxymorphone, morphine, hydromorphone
  2. Have taken an investigational product in the last 30 days
  3. Current use of illicit substances
  4. Immediate family members of site staff, or site staff may not be enrolled in the study without first obtaining IRB authorization
  5. Any other medical, cognitive or physical abnormality, disease, or disorder that would prohibit the patient from completing study procedures in the judgement of the investigator
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
2,500 participants (estimated)
Patient registry
No

Interventions

  • OtherPharmacogenetic Test

    Cheek swab sample with PGx results lab analysis

06

What researchers measure

Primary outcomes

  1. Measure the feasibility of Clinical Decision Support System (MedWise(TM)) for CYP2D6 opioid prescription and PGx recommendations by usability and acceptability through physician and pharmacist questionnaire.

    Quantitative data reported via survey

    Time frame: 6 months

  2. Measure the feasibility of Clinical Decision Support System (MedWise(TM)) for PGx recommendations by acceptability through physician and pharmacist questionnaire.

    Quantitative data reported via survey

    Time frame: 6 months

  3. Measure the feasibility of Clinical Decision Support System (MedWise(TM)) for PGx recommendations by usability through physician and pharmacist questionnaire.

    Quantitative data reported via survey

    Time frame: 6 months

  4. Analyze patient medication information for PGx- and DDI-guided recommendations using MedWise(TM) a proprietary clinical decision support system by Tabula Rasa HealthCare.

    Quantitative (software is proprietary and patented)

    Time frame: 6 months

  5. Analyze clinician uptake of PGx- and DDI-guided recommendations using MedWise(TM) a proprietary clinical decision support system by Tabula Rasa HealthCare.

    Quantitative (software is proprietary and patented)

    Time frame: 6 months

  6. Validate patient QOL questionnaire for disease-related information

    Quantitative data measured by percentage of improvement for DDI-guided recommendations based on PGx results

    Time frame: 6 months

  7. Validate patient QOL questionnaire for pharmacogenetics information

    Quantitative data measured by percentage of improvement for DDI-guided recommendations based on PGx results

    Time frame: 6 months

  8. Validate patient QOL questionnaire for medication-related information, and pharmacogenetics information

    Quantitative data measured by percentage of improvement for DDI-guided recommendations based on PGx results

    Time frame: 6 months

  9. Validate patient QOL questionnaire for socio-demographics

    Quantitative data measured by percentage of improvement for DDI-guided recommendations based on PGx results

    Time frame: 6 months

07

Study locations

1 site
  • Tabula Rasa HealthCare Precision Pharmacotherapy Research and Development Institute
    Orlando, Florida 32827, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jul 2021 (actual). Primary completion is estimated for Jun 2023, 23 months after the start.

Of 154 observational studies under Pain, half reached primary completion within 23 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 71. This study's planned 23 months is close to that.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 15, 2021
First posted
Jul 22, 2021
StartActual
Jul 1, 2021
Primary completionEst.
Jun 30, 2023
CompletionEst.
Aug 31, 2024
Last update
Sep 2, 2022
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 2, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04971902
Lead sponsor
Tabula Rasa HealthCare
Responsible party
Sponsor
First posted
Jul 22, 2021
Start date
Jul 1, 2021
Primary completion
Jun 30, 2023 (estimated)
Completion
Aug 31, 2024 (estimated)
Last update
Sep 2, 2022

Study contacts

Veronique Michaud, PhD
principal investigator · Tabula Rasa HealthCare

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion