Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12607000083493
Ethics application status
Approved
Date submitted
7/11/2006
Date registered
24/01/2007
Date last updated
25/10/2007
Type of registration
Prospectively registered

Titles & IDs
Public title
A Cluster Randomised controlled trial of an Automated versus manual device for Blood pressure management.
Scientific title
A cluster randomised controlled trial of the effect of general practitioner blood pressure measurement of all patients aged 18 years or over who present during the study week, using automated or manual blood pressure device on digit preference, number of measurements (overall and per individual), prescribing of antihypertensive medications, dose adjustments, and mean systolic and diastolic blood pressure.
Universal Trial Number (UTN)
Trial acronym
CRAB
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Blood pressure measurement 1575 0
Condition category
Condition code
Public Health 1677 1677 0 0
Health service research

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
GP participants in practices randomised to receive automated blood pressure measuring device, the OMRON HEM-907 in all clinical rooms.
The duration of the intervention will be one week after an initial 1 week run-in phase.
Blood pressure recordings of all patients aged 18 years or more and hypertension management (where relevant) is determined by research nurses auditing clinical records once after the trial week.
Both the number and level of blood pressure is determined by searching electronic and paper clinical records of the patient for the study week and recording each on an audit sheet.
Intervention code [1] 1433 0
Diagnosis / Prognosis
Comparator / control treatment
GP participants in practices randomised to control will use usual practice.
Control group
Active

Outcomes
Primary outcome [1] 2323 0
Digital preference in blood pressure recordings (1mmHg tolerance in automated devices, 2mmHg in manual).
Timepoint [1] 2323 0
Audit of clinical record once after the study week.
Secondary outcome [1] 4051 0
BP recordings made overall and per individual
Timepoint [1] 4051 0
Audit of clinical record once after the study week.
Secondary outcome [2] 4052 0
prescriptions of antihypertensive medications
Timepoint [2] 4052 0
Audit of clinical record once after the study week.
Secondary outcome [3] 4053 0
dose adjustments of antihypertensive medications
Timepoint [3] 4053 0
Audit of clinical record once after the study week.
Secondary outcome [4] 4054 0
Mean of systolic blood pressure recordings
Timepoint [4] 4054 0
Audit of clinical record once after the study week.
Secondary outcome [5] 4055 0
Mean of diastolic blood pressure recordings
Timepoint [5] 4055 0
Audit of clinical record once after the study week.

Eligibility
Key inclusion criteria
Inclusion criteria: General practices where at least one registered and practicing general practitioner has signed informed consent.
Minimum age
18 Years
Maximum age
Not stated
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Exclusion criteria. General practices where automated blood pressure devices are currently used.

Study design
Purpose of the study
Diagnosis
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Central cluster randomisation of general practices.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation by using a randomization table created by a computer software
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Phase 4
Type of endpoint/s
Efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
1/02/2007
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
24
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)

Funding & Sponsors
Funding source category [1] 1823 0
Charities/Societies/Foundations
Name [1] 1823 0
High Blood Pressure Research Council of Australia
Country [1] 1823 0
Australia
Primary sponsor type
Other
Name
Menzies Research Institute
Address
Private Bag 33
Hobart TAS 7001
Country
Australia
Secondary sponsor category [1] 1643 0
None
Name [1] 1643 0
Nil
Address [1] 1643 0
Country [1] 1643 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 3410 0
Tasmanian Health and Medical Human Research Ethics Committee
Ethics committee address [1] 3410 0
Ethics committee country [1] 3410 0
Australia
Date submitted for ethics approval [1] 3410 0
Approval date [1] 3410 0
09/10/2006
Ethics approval number [1] 3410 0
H9092

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 27367 0
Address 27367 0
Country 27367 0
Phone 27367 0
Fax 27367 0
Email 27367 0
Contact person for public queries
Name 10622 0
Mark Nelson
Address 10622 0
Menzies Research Institute
Private Bag 33
43 Collins St
Hobart TAS 7001
Country 10622 0
Australia
Phone 10622 0
+61 3 62264734
Fax 10622 0
+61 3 62264770
Email 10622 0
[email protected]
Contact person for scientific queries
Name 1550 0
Mark Nelson
Address 1550 0
Menzies Research Institute
Private Bag 33
43 Collins St
Hobart TAS 7001
Country 1550 0
Australia
Phone 1550 0
+61 3 62264734
Fax 1550 0
+61 3 62264770
Email 1550 0
[email protected]

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.