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Randomised controlled trial and economic evaluation of domiciliary medication review by pharmacists in Norfolk & Suffolk
Source of recordUK Trials
ISRCTNISRCTN06813178
Date ISRCTN assigned11/02/2003
Local reference number(s)G106/991
Public titleRandomised controlled trial and economic evaluation of domiciliary medication review by pharmacists in Norfolk & Suffolk
Scientific title
AcronymThe HOMER trial
Disease/condition/study domainNot Applicable
Study hypothesisTo determine whether domiciliary medication review leads to reductions in emergency hospital admissions and an improvement in quality of life compared to standard care among elderly subjects (80 years old and over).
Design/methodologyRandomised controlled trial
Research ethics reviewNot provided at time of registration.
Countries of trialUnited Kingdom
Participants - inclusion criteria1. Discharged after an emergency hospital admission
2. 80 years and over
3. Prescribed two or more daily medications
4. Living in own home or warden controlled accommodation
5. Norfolk or Suffolk resident
Participants - exclusion criteriaLiving in a residential or nursing home.
Patient information material
Anticipated start date01/01/2001
Anticipated end date31/12/2004
Status of trialCompleted
Target number of participants850
InterventionsTwo groups:

Control group received standard care (whatever that entails).

Intervention group are referred to a review pharmacist. The review pharmacist will complete a standard medication review form and will then arrange a home visit at a time when they can meet the patient and any carers helping them with their drugs. The home visit will include a brief assessment of their ability to self-medicate and an assessment of drug compliance. The review pharmacist will, where appropriate:
a. Educate the patient/carer
b. Remove out-of-date drugs (with the patient's consent)
c. Feedback to the GP possible drug reactions/interactions
d. Feedback to the local pharmacist the need for a compliance aid.

One follow-up visit will occur at 6-8 weeks post-recruitment to allow reinforcement of the original advice.
Primary outcome measure(s)Total number of emergency hospital admissions by 6-months
Secondary outcome measure(s)1. Total number of emergency hospital admissions by 3 months
2. Hospital/nursing/residential home admissions for respite care by 3 & 6 months
3. Admissions to nursing/residential care for long-term care by 3 & 6 months
4. Deaths by 3 & 6 months
5. Self-assessed quality of life at 3 & 6 months (using EQ-5D)
6. Average medication costs at 6 months
PublicationsResults: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids= 15665005
Sources of fundingNHS Eastern Region R&D (reference number: HSR/1199/2) (UK)
Medical Research Council (reference number: G106/991) (UK)
Norfolk Health Authority (no reference number allocated) (UK)
Norfolk Social Services (no reference number allocated) (UK)
Suffolk Social Services (no reference number allocated) (UK)
Pharmacy Practice Unit, UEA (no reference number allocated) (UK)
Sponsor nameMedical Research Council (UK)
Sponsor details20 Park Crescent
London
United Kingdom
W1B 1AL
Sponsor telephone+44 (0)20 7636 5422
Sponsor fax+44 (0)20 7436 6179
Sponsor emailclinical.trial@headoffice.mrc.ac.uk
Sponsor websitehttp://www.mrc.ac.uk
Contact nameDr Richard Holland
Contact detailsSchool of Medicine
Health Policy & Practice
University of East Anglia
Norfolk
Norwich
United Kingdom
NR4 7TJ
Contact telephone+44 (0)1603 593574
Contact fax+44 (0)1603 593752
Contact emailr.holland@uea.ac.uk
More informationFor more up-to-date information please go to the ISRCTN link below.
Link to record in ISRCTN RegisterISRCTN06813178
Date last extracted from ISRCTN register17/04/2008
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