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Electronic Monitoring and Improvement of Adherence to DOACs in Polymedicated Stroke Patients (MAAESTRO)

Primary Purpose

Adherence, Patient, Stroke, Ischemic

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Medication intake reminders
Pillbox use and counselling
Sponsored by
University Hospital, Basel, Switzerland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Adherence, Patient focused on measuring ischemic stroke, direct oral anticoagulants, adherence, electronic monitoring, adherence-improving intervention, polypharmacy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Signed informed consent form (ICF)
  • Adult patients (≥ 18 years)
  • Hospitalization for acute ischaemic stroke (including TIA with positive neuroimaging)
  • DOAC treatment for atrial fibrillation or embolic stroke of undetermined source
  • Patients receiving polypharmacy, defined as at least 3 drugs (including DOAC treatment)
  • Patients self-administering their medication
  • Patients already using a pillbox or willing to use one

Exclusion Criteria:

  • Patients not able or unwilling to sign ICF
  • Medication administration by caregiver - Filling of the pillbox by a pharmacy, relatives or other caregivers does not exclude the patients, provided that they self-administer their medication
  • Patients who are, in the opinion of the investigator, unlikely to adhere to the study schedule or are unsuitable for any other reason

Sites / Locations

  • University Hospital Basel

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Group 1

Group 2

Arm Description

Intake reminders followed by crossover to no intake reminders

No intake reminders followed by crossover to intake reminders

Outcomes

Primary Outcome Measures

Change of non-optimal timing adherence to DOACs
Non-optimal timing adherence is defined as at least one DOAC dose not recorded or recorded outside of 25% of the prescribed dosing time schedule

Secondary Outcome Measures

Change of non-optimal taking adherence to DOACs
Non-optimal taking adherence to DOACs is defined as at least one DOAC dose not recorded
Change of timing adherence to DOACs
Timing adherence to DOACs is defined as the proportion of prescribed DOAC doses taken within 25% of the prescribed dosing time schedule
Change of taking adherence to DOACs
Taking adherence to DOACs is defined as the proportion of prescribed DOAC doses taken.
Self-reported adherence to DOACs
Self-reported adherence to DOACs is captured on various questionnaires
Clinical vascular events or death
Recurrent ischaemic stroke or TIA, intracranial hemorrhage, major extracranial hemorrhage, myocardial infarction, venous thromboembolism and death

Full Information

First Posted
November 9, 2017
Last Updated
December 20, 2022
Sponsor
University Hospital, Basel, Switzerland
Collaborators
University of Basel, Clinical Trial Unit, University Hospital Basel, Switzerland
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1. Study Identification

Unique Protocol Identification Number
NCT03344146
Brief Title
Electronic Monitoring and Improvement of Adherence to DOACs in Polymedicated Stroke Patients
Acronym
MAAESTRO
Official Title
Electronic Monitoring and Improvement of Adherence to Direct Oral Anticoagulant Treatment - a Randomised Crossover Study of an Educational and Reminder-based Intervention in Ischaemic Stroke Patients Under Polypharmacy
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
December 1, 2017 (Actual)
Primary Completion Date
March 14, 2022 (Actual)
Study Completion Date
March 14, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Basel, Switzerland
Collaborators
University of Basel, Clinical Trial Unit, University Hospital Basel, Switzerland

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Primary objective of the MAAESTRO trial is to evaluate the impact of an educational and reminder-based intervention on the adherence of stroke patients to DOACs. Secondary objectives are to evaluate the association between non-adherence and clinical events, to identify predictors of non-adherence and to compare objective measures of adherence with self-reporting. Key methodological instrument for this study will be the "Time4Med" pillbox with Smart/ Reminder Card. The study includes 3 visits (baseline visit 0, follow-up visit 1 and end-of-study visit 2) with a total follow-up of 9 months. After an initial 3-month observational phase with electronic monitoring of adherence using the "Smart Card", all patients will receive counselling based on their electronically recorded drug intake data, as well as a multicompartment pillbox. Patients will be then randomised to one of two groups in a crossover design, so that in the subsequent 6-month interventional phase one group will use a (reminder-delivering) "Reminder Card" for the first 3 months and the "Smart Card" for the last 3 months, while the second group will use the cards in reverse order.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adherence, Patient, Stroke, Ischemic
Keywords
ischemic stroke, direct oral anticoagulants, adherence, electronic monitoring, adherence-improving intervention, polypharmacy

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
130 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group 1
Arm Type
Other
Arm Description
Intake reminders followed by crossover to no intake reminders
Arm Title
Group 2
Arm Type
Other
Arm Description
No intake reminders followed by crossover to intake reminders
Intervention Type
Behavioral
Intervention Name(s)
Medication intake reminders
Intervention Description
Acoustic and visual alarm at predefined DOAC-intake timepoints.
Intervention Type
Behavioral
Intervention Name(s)
Pillbox use and counselling
Intervention Description
All patients will be counselled based on their previous electronically recorded adherence data and will be given a multicompartment pillbox für daily use
Primary Outcome Measure Information:
Title
Change of non-optimal timing adherence to DOACs
Description
Non-optimal timing adherence is defined as at least one DOAC dose not recorded or recorded outside of 25% of the prescribed dosing time schedule
Time Frame
0 - 3 months, 3 - 6 months, 6 - 9 months
Secondary Outcome Measure Information:
Title
Change of non-optimal taking adherence to DOACs
Description
Non-optimal taking adherence to DOACs is defined as at least one DOAC dose not recorded
Time Frame
0 - 3 months, 3 - 6 months, 6 - 9 months
Title
Change of timing adherence to DOACs
Description
Timing adherence to DOACs is defined as the proportion of prescribed DOAC doses taken within 25% of the prescribed dosing time schedule
Time Frame
0 - 3 months, 3 - 6 months, 6 - 9 months
Title
Change of taking adherence to DOACs
Description
Taking adherence to DOACs is defined as the proportion of prescribed DOAC doses taken.
Time Frame
0 - 3 months, 3 - 6 months, 6 - 9 months
Title
Self-reported adherence to DOACs
Description
Self-reported adherence to DOACs is captured on various questionnaires
Time Frame
0 - 6 months
Title
Clinical vascular events or death
Description
Recurrent ischaemic stroke or TIA, intracranial hemorrhage, major extracranial hemorrhage, myocardial infarction, venous thromboembolism and death
Time Frame
up to 9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Signed informed consent form (ICF) Adult patients (≥ 18 years) Hospitalization for acute ischaemic stroke (including TIA with positive neuroimaging) DOAC treatment for atrial fibrillation or embolic stroke of undetermined source Patients receiving polypharmacy, defined as at least 3 drugs (including DOAC treatment) Patients self-administering their medication Patients already using a pillbox or willing to use one Exclusion Criteria: Patients not able or unwilling to sign ICF Medication administration by caregiver - Filling of the pillbox by a pharmacy, relatives or other caregivers does not exclude the patients, provided that they self-administer their medication Patients who are, in the opinion of the investigator, unlikely to adhere to the study schedule or are unsuitable for any other reason
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philippe A Lyrer, MD
Organizational Affiliation
University Hospital Basel, Stroke Center and Department of Neurology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kurt Hersberger, MSc, PhD
Organizational Affiliation
University of Basel, Department of Pharmaceutical Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Basel
City
Basel
ZIP/Postal Code
4031
Country
Switzerland

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34081196
Citation
Dietrich F, Polymeris AA, Verbeek M, Engelter ST, Hersberger KE, Schaedelin S, Arnet I, Lyrer PA. Impact of the COVID-19 lockdown on the adherence of stroke patients to direct oral anticoagulants: a secondary analysis from the MAAESTRO study. J Neurol. 2022 Jan;269(1):19-25. doi: 10.1007/s00415-021-10631-5. Epub 2021 Jun 3.
Results Reference
derived
PubMed Identifier
33333334
Citation
Albert V, Polymeris AA, Dietrich F, Engelter ST, Hersberger KE, Schaedelin S, Lyrer PA, Arnet I. Insights Into Direct Oral Anticoagulant Therapy Implementation of Stroke Survivors with Atrial Fibrillation in an Ambulatory Setting. J Stroke Cerebrovasc Dis. 2021 Feb;30(2):105530. doi: 10.1016/j.jstrokecerebrovasdis.2020.105530. Epub 2020 Dec 14.
Results Reference
derived
PubMed Identifier
30622509
Citation
Polymeris AA, Albert V, Hersberger KE, Engelter ST, Schaedelin S, Arnet I, Lyrer PA. Protocol for MAAESTRO: Electronic Monitoring and Improvement of Adherence to Direct Oral Anticoagulant Treatment-A Randomized Crossover Study of an Educational and Reminder-Based Intervention in Ischemic STROke Patients Under Polypharmacy. Front Neurol. 2018 Dec 21;9:1134. doi: 10.3389/fneur.2018.01134. eCollection 2018.
Results Reference
derived

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Electronic Monitoring and Improvement of Adherence to DOACs in Polymedicated Stroke Patients

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