Evaluating the Impact of the Eating Matters Program on the Nutritional Status of Medical Rehab Patients at Joseph Brant Hospital

ConditionFood Intake
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age65+
SponsorJoseph Brant Hospital

About this trial

This research study will determine the impact of the Eating Matters Program on the nutritional status of elderly patients at Joseph Brant Hospital. The Eating Matters Program at Joseph Brant Hospital is a volunteer-based feeding assistance program that aims to improve patients' nutritional intake by providing assistance during mealtimes. As research on the impact of such programs on food intake is limited in Canada, this study will explore how the Eating Matters Program influences protein and energy intake of patients at Joseph Brant Hospital. Further, this study will explore if the hypothesized increase in protein and energy intake with the initiation of the Eating Matters Program is correlated with a decreased risk of malnutrition.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients 65 years and over admitted to Medicine and Rehabilitation units at Joseph Brant Hospital with an anticipated stay 10-14 days

Patients with a Subjective Global Assessment score of B or C, and identified to require eating assistance

Patients able to provide consent or have a Power of Attorney to do so on their behalf

Disqualifiers

Patients that are NPO status (nothing by mouth)

Patients that require enteral or total parenteral feeding

Palliative care patients

Severe cognitive impairment

Trial design

Design model

Parallel

Treatments tested in this trial

  • Feeding Assistance

    Behavioral

    Patients will be receiving assistance during mealtimes. This includes assistance by opening packages, listing/explaining the food products on the tray, providing encouragement and companionship during mealtimes and directly feed patients.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Study Group AExperimental treatment 1 intervention
Group B: Control Group BNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Dietary Intake

Protein and Energy Intake

Time frame
To assess a change from baseline to energy and protein intake post program initiation at the one and two week mark (+/-2days).

Secondary outcomes

Other outcomes

1

Percent weight change

Participants' weight will be measured.

Time frame
A change from baseline body weight at 1 week and 2 weeks marks (+/-2) days post the initiation of the Eating Matters Program (EMP).
2

Handgrip strength

Handgrip strength measured using hand dynamometers.

Time frame
A change from baselines in handgrip measure at 1 and 2 weeks marks (+/-2 days) post the initiation of EMP.
3

C-Reactive Protein

C-Reactive Protein will be measured via routine lab work.

Time frame
A change from baselines CRP at 1 week and 2 weeks marks (+/-2 days) post the initiation of EMP.
4

Eating Matters Program Feedback

Perceptions of program implementation and Barriers to food intake will be evaluated via feedback forms.

Time frame
This will be measured on day 19 (+/-2 days) (total study period for each participant).

Sponsors and contacts

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Joseph Brant Hospital

Lead sponsor

Western University

Collaborator