Leveraging policy to reduce chronic opioid use by educating and empowering community dwelling adults: a study protocol for the TAPERING randomized controlled trial.
Analgesics, Opioid
/ administration & dosage
Chronic Pain
/ diagnosis
Deprescriptions
Drug Administration Schedule
Drug Substitution
Health Knowledge, Attitudes, Practice
Health Policy
Humans
Manitoba
Opioid-Related Disorders
/ diagnosis
Pamphlets
Patient Education as Topic
/ methods
Policy Making
Postal Service
Pragmatic Clinical Trials as Topic
Prospective Studies
Protective Factors
Risk Assessment
Risk Factors
Time Factors
Analgesics
Chronic pain
Deprescribing
Government
Opioids
Patient education
Policy
Journal
Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253
Informations de publication
Date de publication:
09 Jul 2019
09 Jul 2019
Historique:
received:
16
11
2018
accepted:
10
06
2019
entrez:
11
7
2019
pubmed:
11
7
2019
medline:
15
1
2020
Statut:
epublish
Résumé
Opioid use has risen to epidemic proportions across Canada, with increasing evidence of harms including accidental overdose and death. Policy-makers have called for effective approaches to promote opioid reduction. One promising method from deprescribing randomized trials is to empower patients through direct-to-patient education. The current trial will evaluate the effectiveness of a government-led mail-out of educational information to adult community-dwelling, chronic opioid users on the reduction of opioids compared to usual care. This is a pragmatic, prospective, cluster randomized, parallel-arm controlled trial, comparing mailed distribution of a direct-to-patient educational brochure for chronic opioid use (intervention arm) to usual care (control arm). Eligible participants from across Manitoba, Canada, will be identified by the Provincial Drug Programs Branch within the Manitoba Health, Seniors and Active Living Department of the Manitoba Government, allocated to primary care providers, and the latter will be randomized in clusters of family medicine practices to achieve a 1:1 ratio. The primary outcome is complete cessation of opioids after 6 months assessed using Drug Program Information Network data. Secondary outcomes include ≥ 25% dose reduction in the mean morphine milligram equivalent (MME) daily dose, reduction of daily dose to < 90 mg MME, or therapeutic switch to another opioid or non-opioid medication. Data will be analyzed using intent-to-treat generalized estimating equations. This trial will test the efficacy of a population-based, wide-scale, government-led direct-to-patient educational initiative to drive reductions in chronic opioid use by community-dwelling adults across Manitoba. ClinicalTrials.gov, ID: NCT03400384 . Registered on 18 January 2018.
Sections du résumé
BACKGROUND
BACKGROUND
Opioid use has risen to epidemic proportions across Canada, with increasing evidence of harms including accidental overdose and death. Policy-makers have called for effective approaches to promote opioid reduction. One promising method from deprescribing randomized trials is to empower patients through direct-to-patient education. The current trial will evaluate the effectiveness of a government-led mail-out of educational information to adult community-dwelling, chronic opioid users on the reduction of opioids compared to usual care.
METHODS
METHODS
This is a pragmatic, prospective, cluster randomized, parallel-arm controlled trial, comparing mailed distribution of a direct-to-patient educational brochure for chronic opioid use (intervention arm) to usual care (control arm). Eligible participants from across Manitoba, Canada, will be identified by the Provincial Drug Programs Branch within the Manitoba Health, Seniors and Active Living Department of the Manitoba Government, allocated to primary care providers, and the latter will be randomized in clusters of family medicine practices to achieve a 1:1 ratio. The primary outcome is complete cessation of opioids after 6 months assessed using Drug Program Information Network data. Secondary outcomes include ≥ 25% dose reduction in the mean morphine milligram equivalent (MME) daily dose, reduction of daily dose to < 90 mg MME, or therapeutic switch to another opioid or non-opioid medication. Data will be analyzed using intent-to-treat generalized estimating equations.
DISCUSSION
CONCLUSIONS
This trial will test the efficacy of a population-based, wide-scale, government-led direct-to-patient educational initiative to drive reductions in chronic opioid use by community-dwelling adults across Manitoba.
TRIAL REGISTRATION
BACKGROUND
ClinicalTrials.gov, ID: NCT03400384 . Registered on 18 January 2018.
Identifiants
pubmed: 31288859
doi: 10.1186/s13063-019-3508-z
pii: 10.1186/s13063-019-3508-z
pmc: PMC6617933
doi:
Substances chimiques
Analgesics, Opioid
0
Banques de données
ClinicalTrials.gov
['NCT03400384']
Types de publication
Clinical Trial Protocol
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
412Subventions
Organisme : Canadian Institutes of Health Research
ID : 201410PHE-PHE- 337814-96399
Pays : Canada
Organisme : Fonds de Recherche du Québec - Santé
ID : 2016/2017-33087
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