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Trial registered on ANZCTR
Registration number
ACTRN12615000568516
Ethics application status
Approved
Date submitted
5/05/2015
Date registered
2/06/2015
Date last updated
24/03/2017
Type of registration
Prospectively registered
Titles & IDs
Public title
Combatting Frailty in Older Men with multifaceted individually tailored intervention including exercise, diet and behavior.
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Scientific title
A single blind randomised trial on combatting frailty in older men through a multifaceted individually tailored interventions including exercise, dietary supplementation, and behavioural activation.
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Secondary ID [1]
286641
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Nil Known
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Universal Trial Number (UTN)
U1111-1169-5746
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Physical medicine/Rehabilitation
295122
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Diet and nutrition
295123
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Mental Health
295124
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Condition category
Condition code
Physical Medicine / Rehabilitation
295228
295228
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0
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Physiotherapy
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Diet and Nutrition
295366
295366
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0
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Other diet and nutrition disorders
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Mental Health
295367
295367
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0
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Depression
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Intervention period is now only six months not 3 years.
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Intervention code [1]
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Early detection / Screening
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Intervention code [2]
291910
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Lifestyle
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Intervention code [3]
291911
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Behaviour
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Comparator / control treatment
No treatment.
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Control group
Active
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Outcomes
Primary outcome [1]
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The composite primary outcome analysis will be based on intention to treat, comparing the survival in the intervention group to the survivial in the control group using cox proportional hazards regression adjusted for age and level of frailty at baseline. Mortality will be determined through two sources- direct contact with next of kin of men unable to be contacted and through mortality register linked data. Residential care admission will be ascertained through next of kin and hospital records as required.
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Assessment method [1]
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Timepoint [1]
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End of six months
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Secondary outcome [1]
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Frailty status as measured by FRAIL scale score.
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Assessment method [1]
314503
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Timepoint [1]
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Baseline and six months
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Secondary outcome [2]
314646
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Health service usage as assessed by HIMS questionnaire responses and linked data, ( including emergency admissions HACC and ACAP data)
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Assessment method [2]
314646
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Timepoint [2]
314646
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Baseline and six months
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Secondary outcome [3]
314647
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Disability as measured by activities of daily living (ADL's).
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Assessment method [3]
314647
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Timepoint [3]
314647
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Baseline and six months
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Secondary outcome [4]
314648
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Physical performance as assessed by
Timed up and Go (TUG),
Step Test: a dynamic test of single leg stance balance(Hill et al, 1996),
Functional Reach test: a dynamic bilateral stance tests of standing balance (Duncan et al,1990),
Timed sit to stand (five times, Tinetti et al, 1995) and
Knee Extension (quadriceps) strength (Lord et al, 2003).
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Assessment method [4]
314648
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Timepoint [4]
314648
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Baseline and six months
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Secondary outcome [5]
314649
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Changes in cognition as assessed using cognition (MMSE) test.
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Assessment method [5]
314649
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Timepoint [5]
314649
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Baseline and six months
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Secondary outcome [6]
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Composite outcome of total number of medications and inapporpriate medications, assessed by validating medications and/or prescriptions.
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Assessment method [6]
314650
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Timepoint [6]
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Baseline and six months
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Secondary outcome [7]
314651
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Falls as self reported in HIMS questionnaire and specifically designed exercise program journal plus linked data.
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Assessment method [7]
314651
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Timepoint [7]
314651
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Baseline and six months
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Secondary outcome [8]
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Changes in depression as assessed by PHQ9 score.
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Assessment method [8]
314787
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Timepoint [8]
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Baseline and six months
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Secondary outcome [9]
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Quality of life as assessed by HIMS questionnaire.
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Assessment method [9]
314788
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Timepoint [9]
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Baseline and six months
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Eligibility
Key inclusion criteria
Men who were previously part of the HIMS cohort study
(Norman et al 2009) who are currently all over the age of 83 years who are frail or prefrail on the FRAIL scale.(McCaul et al, 2015)
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Minimum age
83
Years
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Maximum age
No limit
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Sex
Males
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Can healthy volunteers participate?
No
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Key exclusion criteria
Exclusion criteria: men with moderate cognitive impairment (MMSE) (Folstein et al, 1975), or who have evidence of major illness likely to cause death within six months.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Allocation concealment using sealed opaque envelopes.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Random generation order using a randomisation table created by computer sequenced generation.
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people assessing the outcomes
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
In both the primary and secondary analyses, we expect that the intervention effect will differ in the men who were pre-frail and the men who were frail at baseline and we will formally test this by fitting an interaction between the intervention variable and baseline frailty. Sample size calculation - we conservatively expect to recruit and randomise 200 men in each arm of the trial. We obtained ABS life tables that estimated the annual age-specific mortality risk by individual age. From AIHW we obtained the number of incident admissions to residential aged care facilites(RACF) by individual age in 2014 and together with ABS estimated resident population counts by individual age, we estimated the age specific risk of RACF admission. From these, we estimated that 55% of participants would be event free (alive and not in RACF) after three years of follow up. Given this, we expect the event risk in Contol arm to be 45% with our expected sample size (200 in each arm) we used Freemans' sample size calculation (Freedman, 1982) for the logrank test to estimate we would have 80% power to detect and event risk of 31% ( i.e. a 30% relative reduction) in the Intervention Arm at the 5% levle of significance.
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Recruitment
Recruitment status
Stopped early
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Data analysis
Data collected is being analysed
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Reason for early stopping/withdrawal
Lack of funding/staff/facilities
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Date of first participant enrolment
Anticipated
1/07/2015
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Actual
5/11/2015
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Date of last participant enrolment
Anticipated
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Actual
28/01/2016
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Date of last data collection
Anticipated
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Actual
31/08/2016
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Sample size
Target
200
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Accrual to date
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Final
76
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Recruitment in Australia
Recruitment state(s)
WA
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Funding & Sponsors
Funding source category [1]
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Government body
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Name [1]
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NHMRC
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Address [1]
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National Health and Medical Research Council
GPO Box 1421
CANBERRA ACT 2601
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Country [1]
291216
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Australia
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Primary sponsor type
Individual
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Name
Professor Leon Flicker
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Address
Western Australian Centre for Health and Ageing (WACHA)
M577 University of Western Australia
35 Stirling H'way
CRAWLEY WA 6009
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Professor Osvaldo Almeida
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Address [1]
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c/- WACHA M577
University of Western Australia
35 Stirling H'way
CRAWLEY WA 6009
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Country [1]
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Australia
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Secondary sponsor category [2]
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Individual
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Name [2]
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Professor Keith Hill
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Address [2]
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Curtin University Faculty of Health Science
School of Physiotherapy & Exercise Science,
408 Level 3
Kent St
BENTLEY WA 6845
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Country [2]
289978
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Australia
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Secondary sponsor category [3]
289979
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Individual
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Name [3]
289979
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Prof Caryl Nowson
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Address [3]
289979
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Deakin University
Faculty of Health
Geelong Waurn Ponds Campus
75 Pigdons Road
Waurn Ponds
GEELONG VIC 3220
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Country [3]
289979
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Australia
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Secondary sponsor category [4]
289980
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Individual
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Name [4]
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Assoc Prof Christopher Etherton-Beer
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Address [4]
289980
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C/- WACHA
University of Western Australia
M577, 35 Stirling H'way
CRAWLEY WA 6009
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Country [4]
289980
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Australia
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Secondary sponsor category [5]
289981
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Individual
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Name [5]
289981
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Assoc Prof Bu Yeap
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Address [5]
289981
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c/- WACHA M577
University of Western Australia
35 Stirling H'way
CRAWLEY WA 6009
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Country [5]
289981
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Australia
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Secondary sponsor category [6]
289982
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Individual
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Name [6]
289982
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Assoc Prof Kieran McCaul
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Address [6]
289982
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c/- WACHA M577
University of Western Australia
35 Stirling H'way
CRAWLEY WA 6009
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Country [6]
289982
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Australia
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Other collaborator category [1]
278470
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Individual
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Name [1]
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Professor Graeme Hankey
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Address [1]
278470
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c/- WACHA M577
University of Western Australia
35 Stirling H'way
CRAWLEY WA 6009
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Country [1]
278470
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Australia
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Other collaborator category [2]
278471
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Individual
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Name [2]
278471
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Professor Paul Norman
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Address [2]
278471
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c/- WACHA M577
University of Western Australia
35 Stirling H'way
CRAWLEY WA 6009
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Country [2]
278471
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Australia
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Other collaborator category [3]
278472
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Individual
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Name [3]
278472
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Professor Jonathon Golledge
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Address [3]
278472
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School of Medicine and Dentistry
Vascular Biology Unit
Douglas Campus
James Cook University
1 James Cook Drive
TOWNSVILLE QLD 4811
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Country [3]
278472
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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University of Western Australia Human Research Ethics Office
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Ethics committee address [1]
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M459 35 Stirling Highway CRAWLEY WA 6009
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
292779
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Approval date [1]
292779
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27/02/2015
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Ethics approval number [1]
292779
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RA/4/1/ 576
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Summary
Brief summary
Frailty is a common syndrome in older adults caused by a decline in reserve capacity of the body's systems used to maintain health. We are interested as to whether interventions for frailty work BEFORE the involvement of clinical services. We propose to undertake a trial of community dwelling older men to determine whether a simple package of interventions can combat this syndrome.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Prof Leon Flicker
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Address
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Director, Western Australian Centre for Health & Ageing (WACHA),
Centre for Medical Research
University of Western Australia
M577 35 Stirling H'way
CRAWLEY WA 6009
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Country
56986
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Australia
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Phone
56986
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618 92243992
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Fax
56986
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618 9224 8009
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Email
56986
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[email protected]
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Contact person for public queries
Name
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Jill George
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Address
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HIMS Study Coordinator
University of Western Australia
M577 35 Stirling H'way
CRAWLEY WA 6009
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Country
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Australia
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Phone
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618 9224 1699
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Fax
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Email
56987
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[email protected]
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Contact person for scientific queries
Name
56988
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Leon Flicker
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Address
56988
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Director, Western Australian Centre for Health & Ageing (WACHA),
Centre for Medical Research
University of Western Australia
M577 35 Stirling H'way
CRAWLEY WA 6009
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Country
56988
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Australia
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Phone
56988
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618 92243992
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Fax
56988
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Email
56988
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[email protected]
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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.
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