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Clinical Trials/NCT02089074
NCT02089074CompletedNot Applicable

Systematic Follow up of Drug Treatment by Pharmacists in Secondary Prevention After Transient Ischemic Attack: Adherence and Cardiovascular Events in the First Three Months

Norwegian University of Science and Technology6 sites in 1 country265 target enrollmentStarted: November 1, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
265
Locations
6
Primary Endpoint
adherence to drug treatment in secondary prevention after TIA

Study Overview

Brief Summary

Use of drugs is an important factor in secondary prophylaxis after transient ischemic attack (TIA), but studies show that adherence to the prescribed drugs is often poor. This randomised controlled trial aims to investigate whether a systematic follow up of drug treatment using medication reconciliation, medication reviews and patient counselling by clinical pharmacists, improves adherence and/or decreases cardiovascular events the first three months and the first year after TIA. Patient satisfaction will also be compared between the two groups.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 90 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Probable or possible transient ischemic attack
  • •Residing in Central Norway
  • •Examined within 2 weeks after the onset of symptoms
  • •Modified Rankin Scale 3 or less and living at home
  • •enrolled in the MIDNOR-TIA study NCT02038725
  • •Informed consent

Exclusion Criteria

  • Not provided

Arms & Interventions

drug use counselling

Experimental

Pharmacist conducting drug reconciliation, medication reviews and drug use counselling during hospitalisation. Follow up telephone calls 1 week, 1 month, 2 months and three months after discharge from hospital

Intervention: Drug use counselling (Behavioral)

Control group

No Intervention

The patients in the control group receive no intervention just treatment and follow up according to national standards

Outcomes

Primary Outcomes

adherence to drug treatment in secondary prevention after TIA

Time Frame: 3 months

self reporting of adherence

Secondary Outcomes

  • adherence to drug treatment in secondary prevention after TIA(1 year)
  • Incidence of stroke and cardiovascular events and deaths(1 year)
  • patient satisfaction(1 year)
  • Persistence(1 year)
  • degree of disability or dependence in the daily activities(1 year)
  • Persistence(3 months)
  • Incidence of stroke and cardiovascular events and deaths(3 months)
  • degree of disability or dependence in the daily activities(3 months)
  • patient satisfaction(3 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (6)

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