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Pharmacist-led home based clinical medication review in stroke
ISRCTN ISRCTN57684399
ClinicalTrials.gov identifier
Public title Pharmacist-led home based clinical medication review in stroke
Scientific title A randomised exploratory trial of a pharmacist-led home based clinical medication review in people after stroke
Acronym N/A
Serial number at source 7874
Study hypothesis Feasibility study of home based pharmacist-led clinical medication review using an evidence based pharmaceutical care plan at 1 month and 3 months after discharge from hospital. Follow up at 6 months.
Lay summary
Ethics approval Lothian Local Research Ethics Committee 03 approved on the 11th June 2009 (ref: 09/S1103/21)
Study design Single centre randomised interventional process of care trial
Countries of recruitment United Kingdom
Disease/condition/study domain Topic: Stroke Research Network; Subtopic: Primary Care; Disease: Community study
Participants - inclusion criteria 1. Patients with stroke due for discharge home from acute, rehabilitation or out-patient neurovascular clinic settings
2. Male and female, aged 53 - 92 years
Participants - exclusion criteria 1. Discharge to long-term care
2. Terminal serious illness
3. Severe confusion such that the patient does not have capacity to understand or give informed consent
4. Unable to nominate a community pharmacy
5. Severe dysphasia
Anticipated start date 21/07/2009
Anticipated end date 06/11/2009
Status of trial Completed
Patient information material Not available in web format, please use the contact details below to request a patient information sheet
Target number of participants Planned sample size: 60; UK sample size: 60
Interventions Pharmacist home-based clinical medication review in people after stroke versus usual care. The pharmacist visits the intervention group at home and uses the pharmaceutical care plan as a structured approach to identify pharmaceutical problems, resolves the problems and communicates with relevant healthcare professionals. Visits are undertaken at 1 month and 3 months after discharge from hospital. All patients are followed up at 6 months with blood pressure measurements being undertaken by independent researchers.

Study entry: single randomisation only
Primary outcome measure(s) Recruitment rate - eligibility and participation. Measured 6 months after recruitment (due for completion May 2010).
Secondary outcome measure(s) At 6 months:
1. EUROQoL
2. Beliefs about Medicines Questionnaire
3. Self-reported adherence
4. Medication adherence
Sources of funding Chief Scientist Office of the Scottish Executive Health Department (UK)
Trial website
Publications
Contact name Ms  Moira  Kinnear
  Address Crewe Road South
  City/town Edinburgh
  Zip/Postcode EH4 2XU
  Country United Kingdom
Sponsor NHS Lothian (UK)
  Address Queens Medical Research Institute
47 Little France Crescent
  City/town Edinburgh
  Zip/Postcode EH16 4TJ
  Country United Kingdom
  Sponsor website: http://www.nhslothian.scot.nhs.uk/
Date applied 12/05/2010
Last edited 13/05/2010
Date ISRCTN assigned 12/05/2010
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