Assessing the intake of nutritional beverages in older adults living in residential care facilities.
- Conditions
- MalnourishedAt risk of malnutritionDiet and Nutrition - Other diet and nutrition disorders
- Registration Number
- ACTRN12622000842763
- Lead Sponsor
- Fonterra Research and Development Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 100
>65 year
Male and female
Identified as malnourished or at risk of malnutrition
Prescribed nutritional supplements
Able to provide informed consent
Living in a residential care facility
<65 years
Cannot provide informed consent
Renal status would contraindicate the consumption of the supplement
Have a terminal illness requiring palliative care
Have a dairy or soy allergy
Require Halal or Kosher diets
Require nasogastric or parental feeding
Recent hospitalisation
Are taking dietary supplements which could influence the outcome of the study
Have a clinical condition that, in the investigator’s judgement, is contraindicated
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Compliance to nutritional beverage as assessed by weighing the amount of the beverage pre- and post-consumption, using a set of digital scales, and calculating the difference. This will be done by the researcher. The participants will be given up to two hours to consume their beverage.[ Twice daily for seven days after the start of the intervention]
- Secondary Outcome Measures
Name Time Method Tolerance - documentation of gastric-related adverse events via a tick box questionnaire filled out by the nursing/care staff,.<br>[ Daily throughout the intervention period];Palatability - assessed through a standardised questionnaire designed and used previously by the sponsor.[ Bi-weekly throughout the intervention period];Satiety - assessed through a standardised questionnaire designed and used previously by the sponsor.[ Bi-weekly throughout intervention period]