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Trial registered on ANZCTR
Registration number
ACTRN12611000408987
Ethics application status
Approved
Date submitted
18/04/2011
Date registered
19/04/2011
Date last updated
28/03/2014
Type of registration
Prospectively registered
Titles & IDs
Public title
Obesity in older adults: effect of exercise and weight loss on physiology and function.
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Scientific title
In obese older adults, is a very low energy diet (VLED) with exercise, a hypocaloric diet with exercise, or exercise alone best to improve physical function?
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Secondary ID [1]
260021
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Nil
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Universal Trial Number (UTN)
U1111-1120-8363
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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:
Obesity
265681
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Condition category
Condition code
Diet and Nutrition
265819
265819
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0
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Obesity
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
ARM 1:Very Low Energy Diet (VLED) - Optifast plus exercise
Optifast is a commercially available Very Low Energy diet.
The diet prescribed to the participants will consist of 1 sachet/bar/soup prepared as per directions on box, for each of breakfast and lunch.
Dinner will consist of a serve of lean protein (lean red meat/fish/tofu) plus a serve of non-starchy vegetables plus a teaspoon of oil to contract the gallbladder.
The target energy intake is 800kCal per day and the duration of the intervention is 12 weeks.
Exercise: 3x45 minute sessions per week, for 12 weeks. The program is called "Heartmoves" and was designed by the National Heart Foundation especially for older people. It involves resistance, balance, strength and endurance components. The intensity of the exercise will be guided by the participant as the moves can be modified. The classes will either be delivered by a trained Heartmoves aerobics instructor or the patient can do the exercise at home by watching a DVD. A physiotherapist will be involved in the study to treat/monitor any injuries.
Arm 2: Hypocaloric Diet Plus exercise
Hypocaloric diet: A diet will be prescribed by a dietician tailored to the participant. The diet will contain enough nutrients for the participant but have fewer calories than what they need (approximately 2000kJ/day deficit from basal requirements), which will result in slow weight loss.
The duration of the intervention will be 12 weeks. The participant will have a long (1 hour) consultation at the beginning of the trial and shorter (approx 30 minute) consultations every 2 weeks during the trial).
The exercise component will be Heartmoves as above.
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Intervention code [1]
264441
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Treatment: Other
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Intervention code [2]
264442
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Behaviour
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Comparator / control treatment
Arm 3: Exercise alone - Heartmoves as above
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Control group
Active
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Outcomes
Primary outcome [1]
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Physical function -
The De Morton Mobility Index (DEMMI) will be used. This is a test of 19 items, from the very basic (bridging in bed) to more advanced (jumping, picking up a pen from the floor). This index is validated in community dwelling older adults.
Other tests of physical function will be the 6 minute walk test and a questionnaire called the human activity profile, which gives a more qualitative account of what the participant can do (eg. walk on uneven ground, walk up steps etc)
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Assessment method [1]
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Timepoint [1]
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0 and 12 weeks
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Secondary outcome [1]
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Cognition - via the Victoria Stroop Interference test, Controlled Oral Word Association Test and Trail Making Tests A and B. These tests are responsive to changes in diet and take about 15 minutes to administer.
We will also be measuring serum ketones at this time
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Assessment method [1]
276041
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Timepoint [1]
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0, 2, 12 and 14 weeks
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Secondary outcome [2]
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Serum Cholesterol and Blood Glucose
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Assessment method [2]
276042
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Timepoint [2]
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0 and 12 weeks
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Secondary outcome [3]
276043
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Blood pressure - supine resting blood pressure measured using a manual sphygmomanometer
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Assessment method [3]
276043
0
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Timepoint [3]
276043
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0, 2,4,6,8,10, 12 and 14 weeks
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Secondary outcome [4]
276044
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Quality of life - the AQoL 8d questionnaire will be used.
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Assessment method [4]
276044
0
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Timepoint [4]
276044
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0 and 12 weeks
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Secondary outcome [5]
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6 minute walk test distance
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Assessment method [5]
301745
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Timepoint [5]
301745
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0 and 12 weeks
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Secondary outcome [6]
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Serum inflammatory markers
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Assessment method [6]
301746
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Timepoint [6]
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0 and 12 weeks
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Secondary outcome [7]
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Body Composition Via Dual Energy XRay Absorptiometry (DEXA)
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Assessment method [7]
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Timepoint [7]
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0 and 12 weeks
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Eligibility
Key inclusion criteria
Age over 65 Body Mass index over 35 One or more complications of obesity - hypertension, obstructive sleep apnoea, osteoarthritis, type 2 diabetes, Living in community (including retirement village)
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Minimum age
65
Years
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Maximum age
85
Years
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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
Living in residential care (hostel or nursing home) Unstable disease state (symptomatic cardiorespiratory disease, brittle diabetes etc) Diseases with a prognosis of less than five years Diseases which have an effect on weight (eg uncontrolled thyroid disease)
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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)
patient enrolled by study doctor. Patients randomised to treatment. Randomisation form kept by person independent to study.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Statistician created block randomisation model stratified for gender and diabetic status
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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
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/06/2011
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Actual
14/02/2012
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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
200
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
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Austin Health - Heidelberg Repatriation Hospital - Heidelberg West
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Recruitment hospital [2]
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The Northern Hospital - Epping
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Recruitment postcode(s) [1]
6584
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3081 - Heidelberg Heights
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Recruitment postcode(s) [2]
6585
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3076 - Epping
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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
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Address [1]
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Level 1
16 Marcus Clarke Street
Canberra ACT 2601
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Country [1]
264910
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Australia
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Funding source category [2]
286899
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Charities/Societies/Foundations
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Name [2]
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Diabetes Australia Research trust
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Address [2]
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Level 1, 101 Northbourne Ave
TURNER ACT 2612
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Country [2]
286899
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Australia
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Primary sponsor type
Hospital
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Name
Austin Health
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Address
Repatriation Campus
Waterdale Road, Heidelberg Heights
Victoria 3084
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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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University of Melbourne
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Address [1]
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Austin Health Department of Medicine
University of Melbourne
Repatriation Campus
Waterdale Road, Heidelberg Heights
Victoria 3084
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Country [1]
264011
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
266869
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Austin Health Human Research Ethics Committee
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Ethics committee address [1]
266869
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Ethics committee country [1]
266869
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Australia
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Date submitted for ethics approval [1]
266869
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05/04/2011
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Approval date [1]
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03/08/2011
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Ethics approval number [1]
266869
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04274
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Ethics committee name [2]
288959
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Northern Health Human Research Ethics Committee
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Ethics committee address [2]
288959
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Cooper St Epping Vic 3076
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Ethics committee country [2]
288959
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Date submitted for ethics approval [2]
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11/12/2012
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Approval date [2]
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05/02/2013
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Ethics approval number [2]
288959
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P19/12
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Summary
Brief summary
This study is to investigate which strategy is best in terms of preserving physical function in older adults (greater than 65 years) who are obese. The interventions are a very low energy diet (VLED - Optifast) plus exercise, diet plus exercise or exercise alone. The trial will last for 12 weeks. We will also look at the effects of these measures on body composition, blood pressure, glucose, cholesterol and memory/thinking.
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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 Joe Proietto
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Address
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2nd Floor
Boronia Building
Heidelberg Repatriation Hospital
Waterdale Rd
Heidelberg Heights Vic 3081
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Country
32507
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Australia
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Phone
32507
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+61394962160
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Fax
32507
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+61394974554
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Email
32507
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[email protected]
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Contact person for public queries
Name
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Cilla Haywood
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Address
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Department of Medicine University of Melbourne
Repatriation Campus, Austin Health
300 Waterdale Rd Heidelberg Heights
Victoria 3084
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Country
15754
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Australia
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Phone
15754
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+61394962879
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Fax
15754
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+61394974554
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Email
15754
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[email protected]
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Contact person for scientific queries
Name
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Joe Proietto
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Address
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Department of Medicine University of Melbourne
Repatriation Campus, Austin Health
300 Waterdale Rd Heidelberg Heights
Victoria 3084
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Country
6682
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Australia
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Phone
6682
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+61394962250
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Fax
6682
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+61394974554
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Email
6682
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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.
Download to PDF