Trial Review

The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT03594097




Registration number
NCT03594097
Ethics application status
Date submitted
10/07/2018
Date registered
20/07/2018
Date last updated
20/03/2023

Titles & IDs
Public title
Use of Coconut Nourish and Queen Garnet Plum to Improve Health in an Elderly Population
Scientific title
Use of Coconut Nourish and Queen Garnet Plum to Improve Health in an Elderly Population
Secondary ID [1] 0 0
HS21905 (B2018:052)
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Healthy Ageing 0 0
Condition category
Condition code

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Other interventions - Treatment cookies
Other interventions - Control cookies

Experimental: Treatment cookies -

Active comparator: Control cookies -


Other interventions: Treatment cookies
Plain flour, Coconut Nourish, Queen Garnet Plum, Unsalted Butter, Artificial Sweetener

Other interventions: Control cookies
Plain flour, Coconut Powder, Unsalted Butter, Artificial Sweetener, Food Colour
Intervention code [1] 0 0
Other interventions
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Lean mass
Timepoint [1] 0 0
8 weeks
Secondary outcome [1] 0 0
Body weight
Timepoint [1] 0 0
8 weeks
Secondary outcome [2] 0 0
Body mass index
Timepoint [2] 0 0
8 weeks
Secondary outcome [3] 0 0
Waist circumference
Timepoint [3] 0 0
8 weeks
Secondary outcome [4] 0 0
Arm circumference
Timepoint [4] 0 0
8 weeks
Secondary outcome [5] 0 0
Wrist circumference
Timepoint [5] 0 0
8 weeks
Secondary outcome [6] 0 0
Calf circumference
Timepoint [6] 0 0
8 weeks
Secondary outcome [7] 0 0
Triceps skinfold
Timepoint [7] 0 0
8 weeks
Secondary outcome [8] 0 0
Five times chair standing test
Timepoint [8] 0 0
8 weeks
Secondary outcome [9] 0 0
Handgrip dynamometer
Timepoint [9] 0 0
8 weeks
Secondary outcome [10] 0 0
Blood pressure
Timepoint [10] 0 0
8 weeks
Secondary outcome [11] 0 0
Heart rate
Timepoint [11] 0 0
8 weeks
Secondary outcome [12] 0 0
Bone mineral density
Timepoint [12] 0 0
8 weeks
Secondary outcome [13] 0 0
Bone mineral content
Timepoint [13] 0 0
8 weeks
Secondary outcome [14] 0 0
Fat mass
Timepoint [14] 0 0
8 weeks
Secondary outcome [15] 0 0
Blood total cholesterol
Timepoint [15] 0 0
8 weeks
Secondary outcome [16] 0 0
Blood low-density lipoprotein cholesterol
Timepoint [16] 0 0
8 weeks
Secondary outcome [17] 0 0
Blood high-density lipoprotein cholesterol
Timepoint [17] 0 0
8 weeks
Secondary outcome [18] 0 0
Blood triglycerides
Timepoint [18] 0 0
8 weeks
Secondary outcome [19] 0 0
Blood glucose
Timepoint [19] 0 0
8 weeks
Secondary outcome [20] 0 0
Blood C-reactive protein
Timepoint [20] 0 0
8 weeks
Secondary outcome [21] 0 0
Blood interleukin 1 beta
Timepoint [21] 0 0
8 weeks
Secondary outcome [22] 0 0
Blood tumor necrosis factor alpha
Timepoint [22] 0 0
8 weeks

Eligibility
Key inclusion criteria
* Aged 65 years and above
* Able to give written informed consent
* Able to read, write and speak English
* Body mass index less than or equal to 30 kg/m^2
* Either do not suffer from a chronic disease or, if suffering from a chronic disease, then key parameters (blood pressure, blood lipids concentration and blood glucose concentrations) are within the normal physiological range
* Either take no chronic medication or have been treated with a stable dosage of medication for at least 3 months as confirmed by family physician.
* Either take no supplements, or have been utilizing supplements in a stable and consistent dose for at least 3 months, and plan to continue taking a stable and consistent dose throughout the entire study.
Minimum age
65 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
* Smokers
* Consumption of more than 2 alcoholic drinks/day, or > 14 alcoholic beverages a week, or history of alcoholism or drug dependence
* Uncontrolled hypertension, recent stroke or myocardial infarction, hypothyroidism, diabetes mellitus or kidney disease
* Major disability or disorder requiring continuous medical attention and treatment such as chronic heart failure, liver disease, renal failure or cancer, chronic infections or major surgery within 6 months prior to randomization
* Despite taking medication, do not have values for key parameters (blood pressure, blood lipids concentration and blood glucose concentrations) within normal physiological ranges
* Fasting glucose = 5.6 mmol/L
* Triglycerides = 1.7 mmol/L
* Systolic and diastolic blood pressures =130/85 mmHg
* High-density lipoprotein cholesterol =1.0 mmol/L
* Have gained or lost >10 lbs in the previous 3 months, or plan to lose weight at any time during the study
* History of allergy to coconut, plum, plain flour, butter or milk
* Any planned surgeries during the study

Study design
Purpose of the study
Prevention
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Crossover
Other design features
Phase
NA
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Stopped early
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
4/09/2018
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
31/08/2019
Sample size
Target
Accrual to date
Final
7
Recruitment in Australia
Recruitment state(s)
QLD
Recruitment hospital [1] 0 0
University of Southern Queensland - Toowoomba
Recruitment postcode(s) [1] 0 0
4350 - Toowoomba
Recruitment outside Australia
Country [1] 0 0
Canada
State/province [1] 0 0
Manitoba

Funding & Sponsors
Primary sponsor type
Other
Name
University of Manitoba
Address
Country
Other collaborator category [1] 0 0
Other
Name [1] 0 0
University of Southern Queensland
Address [1] 0 0
Country [1] 0 0

Ethics approval
Ethics application status

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

Contacts
Principal investigator
Name 0 0
Peter Jones, PhD
Address 0 0
University of Manitoba
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

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

No documents have been uploaded by study researchers.

Results not provided in https://clinicaltrials.gov/study/NCT03594097