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
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
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
NCT ID
NCT03344146
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
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
Learn more about this trial
Electronic Monitoring and Improvement of Adherence to DOACs in Polymedicated Stroke Patients
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