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Trial registered on ANZCTR
Registration number
ACTRN12616000310460
Ethics application status
Approved
Date submitted
25/02/2016
Date registered
9/03/2016
Date last updated
14/10/2016
Type of registration
Prospectively registered
Titles & IDs
Public title
Optimal Nutrition in the Elderly: High Protein Diets for Muscular Metabolic, and Microbiome Health
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Scientific title
The effects of 10 weeks of high or low protein intake on muscular strength, metabolism and faecal microbiome in elderly men
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Secondary ID [1]
288619
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NIL
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Universal Trial Number (UTN)
U111111765813
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Trial acronym
OptiMuM
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Sarcopenia
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Condition category
Condition code
Diet and Nutrition
297958
297958
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0
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Other diet and nutrition disorders
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Musculoskeletal
298102
298102
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0
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Other muscular and skeletal disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants will consume a controlled diet provided by the experimenters for 10 weeks. The diet will provide 1.6 g/kg/day of protein and will meet energy needs for each participant based on the Harris-Benedict equation. The diet will also consist of approximately 30% fat and 50% carbohydrate. Participants will be asked to record any food not consumed in a food diary.
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Intervention code [1]
294023
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Lifestyle
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Intervention code [2]
294140
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Prevention
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Intervention code [3]
294141
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Treatment: Other
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Comparator / control treatment
Participants will consume a controlled diet provided by the experimenters for 10 weeks. The diet will provide 0.8 g/kg/day of protein and will meet energy needs for each participant based on the Harris-Benedict equation. The diet will also consist of approximately 30% fat and 60% carbohydrate. Participants will be asked to record any food not consumed in a food diary.
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Control group
Dose comparison
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Outcomes
Primary outcome [1]
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Isometric knee extension strength measured on a Biodex dynamometer
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Assessment method [1]
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Timepoint [1]
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Baseline, post intervention (10 week)
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Primary outcome [2]
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lean body mass measured with DXA
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Assessment method [2]
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Timepoint [2]
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Baseline, post intervention (10 weeks)
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Primary outcome [3]
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Insulin sensitivity measured by oral glucose tolerance test
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Assessment method [3]
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Timepoint [3]
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Baseline, post intervention (10 week)
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Secondary outcome [1]
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Thigh muscle cross sectional area as measured by pqCT
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Assessment method [1]
321151
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Timepoint [1]
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Baseline, post intervention (10 week)
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Secondary outcome [2]
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Short physical performance battery score
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Assessment method [2]
321169
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Timepoint [2]
321169
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Baseline, post intervention (10 week)
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Secondary outcome [3]
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quality of life assessed using the SF-36 Quality of Life Questionnaire
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Assessment method [3]
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Timepoint [3]
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Baseline, post intervention (10 week)
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Secondary outcome [4]
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Gut microbiome composition measured with faecal RNA sequencing
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Assessment method [4]
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Timepoint [4]
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Baseline, Post intervention (10 week)
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Secondary outcome [5]
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Muscle fibre size measured with a muscle biopsy
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Assessment method [5]
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Timepoint [5]
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Baseline, Post intervention (10 week)
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Eligibility
Key inclusion criteria
*Healthy community dwellers (activities of daily living preformed unassisted)
*BMI (18-35 kg/m2)
*Sedentary to moderately active (structured activity of less than 4 hours per week)
*No history of gastrointestinal disease or disturbance, or antibiotics use in the previous 3 months, or probiotic use in the preceding one month. Normal bowel frequency (minimum once every 2 days, maximum 3 times per day)
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Minimum age
70
Years
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Maximum age
No limit
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Sex
Males
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
*Receiving dietetic intervention or prescribed dietary supplements in the last month, including calcium and fish oil.
*Receiving palliative care
*History of alcohol abuse
*Smoking
*Participation in an investigational drug evaluation
*On medications which may affect the muscle: however, ACE inhibitors, statins and calcium channel blockers will be allowed.
*Advanced organic diseases: cardiac illness; myocardial infarction; thrombophlebitis; cerebrovascular disease
*Major systemic disease diagnosed or active within the previous 20 years (e.g. cancer, rheumatoid arthritis)
*Osteoarthritis, classified by inability to perform maximal contractions of upper and lower limbs without pain
*Acute febrile illness within the previous 6 months
*Metabolic disease (e.g. diabetes, obesity, thyroid disease)
*Meat or dairy allergy, vegetarian
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Study design
Purpose of the study
Prevention
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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 is concealed using a lock spreedsheet
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
randomization sequence was generated with Random.org
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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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
Efficacy
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Statistical methods / analysis
Two way ANOVA with diet as a between subject factor and time as a within subject factor will be used. A total of 30 subjects with 15 subjects each in the 2 treatment arms will be required to achieve a power of 80% and a significance of 5% for the comparison between treatment and control arms. These calculations are based on the variance in appendicular muscle mass (as measured by DXA) from (Gregorio, et al., 2014), effect size was also based on an extrapolation of these data.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
29/03/2016
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Actual
6/04/2016
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Date of last participant enrolment
Anticipated
31/08/2016
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Actual
14/07/2016
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Date of last data collection
Anticipated
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Actual
5/10/2016
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Sample size
Target
30
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Accrual to date
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Final
29
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Recruitment outside Australia
Country [1]
7616
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New Zealand
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State/province [1]
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Auckland
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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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Ministry of Business, Innovation and Employment
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Address [1]
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15 Stout Street, Wellington 6011
PO Box 1473, Wellington 6140
New Zealand
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Country [1]
292982
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New Zealand
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Primary sponsor type
University
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Name
University Of Auckland
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Address
The University of Auckland
Private Bag 92019
Auckland 1142
New Zealand
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Country
New Zealand
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Secondary sponsor category [1]
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None
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Name [1]
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NIL
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Address [1]
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NIL
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Country [1]
291752
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Health and Dissablity Ethics Committees (southern)
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Ethics committee address [1]
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Ministry of Health Ethics Department Freyberg Building Reception – Ground Floor 20 Aitken Street Wellington 6011
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Ethics committee country [1]
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New Zealand
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Date submitted for ethics approval [1]
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19/11/2015
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Approval date [1]
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24/02/2016
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Ethics approval number [1]
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15/STH/236
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Summary
Brief summary
40 healthy men age 70+ years old will be randomized to consume a weight maintenance diet containing either 0.8 or 1.6 g/kg/day of protein for 10 weeks. Muscle size, strength, lean body mass, physical function (SPPB and timed up and go), insulin sensitivity and gut microbiome composition will be measured before and after the 10 week dietary intervention period. Muscle fibre size will be measured via muscle biopsies taken before and after the intervention period.
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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 David Cameron-Smith
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Address
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Liggins Institute
The University of Auckland
Private Bag 92019
Victoria Street West
Auckland 1142
New Zealand
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Country
63886
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New Zealand
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Phone
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+64 9 923 1336
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Cameron Mitchell
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Address
63887
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Liggins Institute
The University of Auckland
Private Bag 92019
Victoria Street West
Auckland 1142
New Zealand
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Country
63887
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New Zealand
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Phone
63887
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+64 9 923 6606
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Fax
63887
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Email
63887
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[email protected]
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Contact person for scientific queries
Name
63888
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Cameron Mitchell
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Address
63888
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Liggins Institute
The University of Auckland
Private Bag 92019
Victoria Street West
Auckland 1142
New Zealand
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Country
63888
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New Zealand
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Phone
63888
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+64 9 923 6606
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Fax
63888
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Email
63888
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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
Source
Title
Year of Publication
DOI
Embase
Protein intake at twice the RDA in older men increases circulatory concentrations of the microbiome metabolite trimethylamine-N-oxide (TMAO).
2019
https://dx.doi.org/10.3390/nu11092207
Embase
Regulation of Amino Acid Transporters and Sensors in Response to a High protein Diet: A Randomized Controlled Trial in Elderly Men.
2019
https://dx.doi.org/10.1007/s12603-019-1171-4
Embase
A period of 10 weeks of increased protein consumption does not alter faecal microbiota or volatile metabolites in healthy older men: A randomised controlled trial.
2020
https://dx.doi.org/10.1017/jns.2020.15
Embase
Responsiveness of one-carbon metabolites to a high-protein diet in older men: Results from a 10-wk randomized controlled trial.
2021
https://dx.doi.org/10.1016/j.nut.2021.111231
Embase
The effect of elevated protein intake on dna damage in older people: Comparative secondary analysis of two randomized controlled trials.
2021
https://dx.doi.org/10.3390/nu13103479
N.B. These documents automatically identified may not have been verified by the study sponsor.
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