Recruiting

Polypharmacy Evaluation

Sponsor:

McMaster University

Code:

NCT03557944

Conditions

Multi-morbidity

Medication Therapy Management

Polypharmacy

Eligibility Criteria

Sex: All

Age: 70+

Healthy Volunteers: Not accepted

Interventions

Medication reduction

Study Details

Brief summary:

In an aging population, most seniors suffer from multiple chronic conditions. When the number of medications taken is ≥5 (polypharmacy), the burden of taking multiple concurrent medications can do more harm than good. Seniors take an average of 7 regular medications and studies link polypharmacy with adverse effects on morbidity, function and health service use. However, it is not clear to what extent these are reversible if medication burden is reduced.

This trial will test the effects on medication numbers and patient health outcomes of an intervention to polypharmacy. This study will test a program focused on medication reduction number and dose. Prioritizing medications according to the patient's preference as reducing the dose also reduces the risk of drug side effects.

Patients, aged 70 years of age or older and taking ≥5 medications will receive the TAPER program. The program involves information gathering from the patient, including systematically seeking patients priorities and preferences, medication review with the pharmacist and then a consultation with the family doctor. The intervention is focused on discontinuing/reducing the dose of medications where possible using a 'pause and monitor' framework to assess the need for restart. An electronic program that detects drug adverse effects and flags potentially inappropriate medications will be integrated into an electronic clinical pathway incorporating monitoring and follow-up systems.

This study will examine whether implementing a deprescribing care pathway with community pharmacists as point-of-entry can signal improvements in prescribing and patient health outcomes in older adults with polypharmacy.

Conditions

Multi-morbidity

Medication Therapy Management

Polypharmacy

Study ID

NCT03557944

Start date

Jun 16, 2019

Status verified date

Mar, 2023

Completion date

Jun, 2024

Anticipated

Primary completion date

Oct, 2023

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Aged 70 years of age or older
  • Patient must have a family doctor
  • Participating family doctor as most responsible provider
  • Currently taking 5 or more long-term medications
  • Has not had a recent comprehensive medication review
  • Patient willing to try discontinuation

Exclusion Criteria:

  • English language or cognitive skills inadequate to understand and respond to rating scales
  • Terminal illness or other circumstance precluding 6 month study period

Study Design

Enrollment

30 participants

Anticipated

Intervention Model

Single group

Primary purpose

Other

Interventions and Outcome Measures

Arms

experimental: TAPER

The intervention is medication reduction. This arm is comprised of:

1. Medication reconciliation
2. Identification of patient priorities for care
3. Identification of medications that are potentially appropriate for discontinuation/dose reduction
4. Linked pharmacist/family physician consultations with patient to discuss medication with intention to reduce
5. Identification of medications for trial of discontinuation/dose reduction (shared decision making)
6. Pause of medication and clinical monitoring

Interventions

Medication reduction

Systematic approach to reduction in polypharmacy.

Primary outcome measure

  • Feasibility (recruitment number) [ Time Frame: 6 months ]

Central Contacts and Locations

Central contacts

Dee Mangin, MBChB, DPH, FRNZC, MD

905-525-9140mangind@mcmaster.ca

Locations

Dr. Dee Mangin

Recruiting

Hamilton, Ontario, Canada, L8S 4K1

Contacts

More Information

Sponsor

McMaster University

Last update posted

Mar 15, 2023

Last verified

Mar, 2023

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by McMaster University on 2023-03-15.