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Hospital Discharge Oral Nutrition Support Trial

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Nutricia

Status

Completed

Conditions

Malnutrition

Treatments

Dietary Supplement: Dietary Advice
Dietary Supplement: Oral Nutritional Supplement 2
Dietary Supplement: Oral Nutritional Supplement 1

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

To investigate the effect of different strategies for managing malnutrition in the community

Enrollment

120 patients

Sex

All

Ages

50+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male or Female
  • Age 50 years and over
  • Able to eat and drink without the need for altered texture fluids
  • Identified at risk of disease related malnutrition
  • Competent to provide written informed consent
  • Willingness to take part in the study and to follow the study protocol

Exclusion criteria

  • Individuals unable to eat or drink
  • Chronic renal disease requiring dialysis
  • Galactosaemia
  • Dysphagia
  • Normally or going to be residing in an institution e.g. care home upon discharge from hospital
  • Palliative care
  • Cancer (active treatment)
  • Liver failure
  • Poorly controlled diabetes
  • Diagnosed lactose intolerance
  • Participation in other clinical trials currently or in the previous 4 weeks
  • Due to be discharged to an area out of the hospital region
  • Requiring tube or parenteral nutrition
  • Due to be discharged from hospital on oral nutrition support recommended by a Dietitian

Trial design

120 participants in 3 patient groups

ONS 1 and DA
Other group
Description:
Oral Nutritional Supplement 1 and Dietary Advice
Treatment:
Dietary Supplement: Dietary Advice
Dietary Supplement: Oral Nutritional Supplement 1
ONS 2 and DA
Other group
Description:
Oral Nutritional Supplement 2 and Dietary Advice
Treatment:
Dietary Supplement: Oral Nutritional Supplement 2
Dietary Supplement: Dietary Advice
DA Alone
Other group
Description:
Dietary Advice Alone
Treatment:
Dietary Supplement: Dietary Advice

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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