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Tailored Intervention to Improve Patient Adherence to Secondary Stroke Prevention Medication

Pharmacist Intervention Programme to Improve Medication Adherence in Stroke Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01684176
Enrollment
211
Registered
2012-09-12
Start date
2012-08-31
Completion date
2014-06-30
Last updated
2015-01-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke, Transient Ischemic Attack

Keywords

Stroke, Ischemic Attack, Transient, Medication adherence, Motivational interviewing, Stroke prevention

Brief summary

Patient suffering a Transient Ischemic Attack (TIA) or stroke are subsequently at high risk of a new stroke, however, poor adherence to secondary prevention medications occurs frequently within this patient group. The purpose of this study is to evaluate whether a complex tailored pharmacist intervention will lead to increased adherence to secondary stroke prevention medications and less new stroke events when compared to a usual care group. Interventions focus on motivational interviewing, medication review and telephone follow up.

Interventions

BEHAVIORALUsual care

Sponsors

University of Southern Denmark
CollaboratorOTHER
Odense University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age: 18 years or older * Patient admitted or receiving ambulatory treatment for an acute transient ischemic attack or ischemic stroke which has occurred within the previous 30 days. * The patient or a carer usually dispenses the patient's medications * Written consent

Exclusion criteria

* Cognitive or physical impairment that would preclude comprehension of a conversation * Terminal illness * Lives in a care home or an institution * Receives dose dispensed medicine from a pharmacy * Medicine is dispensed by a nurse in the patient's home * Correctional mental health patients

Design outcomes

Primary

MeasureTime frame
Medication Adherence to antiplatelets, anticoagulants and statins measured by proportion of days covered (PDC).One year from inclusion
For antiplatelets, anticoagulants and statins: Percent of patients that are at least 80% adherent (PDC>0.8)1 year from inclusion

Secondary

MeasureTime frame
Non-persistence with thromboprophylactic agents ( antiplatelets, anticoagulants, statins and antihypertensives) measured by percent of patients that are not supplied with medication for more than 3 continuous monthsOne year from inclusion
Medication Adherence to antihypertensives measured by proportion of days covered (PDC)One year from inclusion
Composite endpoint: stroke, myocardial infarction or cardiovascular deathOne year from inclusion
Accept rate for thromboprophylactic agents measured by percent of patients starting treatment within 0-90 days after discharge.3 months from discharge
Percent of patients that are at least 80% adherent (PDC>0.8) to antihypertensivesOne year from inclusion

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026