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Trial registered on ANZCTR
Registration number
ACTRN12607000017426
Ethics application status
Not yet submitted
Date submitted
18/12/2006
Date registered
10/01/2007
Date last updated
10/01/2007
Type of registration
Prospectively registered
Titles & IDs
Public title
Individual Nutrition Therapy and Exercise Regime: A Controlled Trial of Injured, Vulnerable Elderly.
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Scientific title
A randomised controlled trial on improving gait speed and other health outcomes for elderly patients with hip fracture using an individualised nutrition and exercise program.
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Universal Trial Number (UTN)
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Trial acronym
INTERACTIVE trial
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Elderly people with a hip fracture
1518
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Condition category
Condition code
Injuries and Accidents
1616
1616
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0
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Fractures
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
6 month individualised exercise (tri-weekly, one hour muscle strengthening, balance training and walking) and nutrition therapy (small, frequent meals plus oral supplements or enteral feeds as appropriate to current nutritional status and nutritional rehabilitation goals) plan.
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Intervention code [1]
1485
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Rehabilitation
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Comparator / control treatment
The control group will receive usual care in addition to social visits to match the attention provided to the intervention group.
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Control group
Active
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Outcomes
Primary outcome [1]
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Gait speed
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Assessment method [1]
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Timepoint [1]
2229
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At 6 months
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Secondary outcome [1]
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Physical function
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Assessment method [1]
3883
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Timepoint [1]
3883
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Fortnightly for 6 months
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Secondary outcome [2]
3884
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Body composition
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Assessment method [2]
3884
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Timepoint [2]
3884
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Fortnightly for 6 months
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Secondary outcome [3]
3885
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QoL
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Assessment method [3]
3885
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Timepoint [3]
3885
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6 months
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Secondary outcome [4]
3886
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Caregiver burden
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Assessment method [4]
3886
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Timepoint [4]
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Weekly for 6 months
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Secondary outcome [5]
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Cost and resource use
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Assessment method [5]
3887
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Timepoint [5]
3887
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Daily for 6 months
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Eligibility
Key inclusion criteria
Patients recovering from proximal femoral fracture (PFF) at Flinders Medical Centre (Adelaide). Ability to understand and comply with the requirements of the study.
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Minimum age
70
Years
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Maximum age
Not stated
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Severe cognitive impairment (MMT <18/30), body mass index <18.5 kg/m2 and >30 kg/m2.
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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)
Sealed opaque envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computerised sequence generation
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
Outcome assessors will be blind to treatment allocation.
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Phase
Phase 4
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
16/04/2007
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
460
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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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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National Health and Medical Research Council (NHMRC) Project Grant
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Address [1]
1763
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Country [1]
1763
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Australia
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Primary sponsor type
University
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Name
Rehabilitation & Ageing Studies Unit, Flinders University
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Address
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Country
Australia
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Secondary sponsor category [1]
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University
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Name [1]
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Nutrition & Dietetics Department, Flinders University
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Address [1]
1562
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Country [1]
1562
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Australia
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Ethics approval
Ethics application status
Not yet submitted
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Ethics committee name [1]
3288
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Flinders Medical Centre / Flinders University
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Ethics committee address [1]
3288
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Ethics committee country [1]
3288
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Australia
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Date submitted for ethics approval [1]
3288
0
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Approval date [1]
3288
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Ethics approval number [1]
3288
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Ethics committee name [2]
3289
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Ryde Hospital
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Ethics committee address [2]
3289
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Ethics committee country [2]
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Australia
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Date submitted for ethics approval [2]
3289
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Approval date [2]
3289
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Ethics approval number [2]
3289
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Ethics committee name [3]
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Hornsby Ku-ring-gai Hospital
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Ethics committee address [3]
3290
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Ethics committee country [3]
3290
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Australia
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Date submitted for ethics approval [3]
3290
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Approval date [3]
3290
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Ethics approval number [3]
3290
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Ethics committee name [4]
3291
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Sydney University
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Ethics committee address [4]
3291
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Ethics committee country [4]
3291
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Australia
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Date submitted for ethics approval [4]
3291
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Approval date [4]
3291
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Ethics approval number [4]
3291
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Summary
Brief summary
This study will use the best quality research methods to test whether providing a 6-month individualised exercise and nutrition program to hip fracture patients soon after injury improves walking and other important health outcomes. Patients will be followed for 12 months to determine what difference the exercise and and nutrition programs make. If they help then health services will have the evidence they need to recommend this type of program to the growing number of older Australians that suffer a hip fracture.
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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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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Dr Michelle Miller
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Address
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Department of Nutrition & Dietetics
Flinders University
G4 Flinders Medical Centre (FMC) Flats
Flinders Drive
Bedford Park SA 5042
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Country
10674
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Australia
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Phone
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+61 8 82045328
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Dr Michelle Miller
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Address
1602
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Department of Nutrition & Dietetics
Flinders University
G4 Flinders Medical Centre (FMC) Flats
Flinders Drive
Bedford Park SA 5042
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Country
1602
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Australia
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Phone
1602
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+61 8 82045328
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Fax
1602
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Email
1602
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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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