Compliance of dairy products versus oral nutrition supplements in patients with a risk for malnutrition.

Compliance of dairy products versus oral nutrition supplements in patients with a risk for malnutrition. - Dairy.Com

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON41996

Enrollment

131

Registered

2015-07-30

Start date

2015-11-02

Completion date

Unknown

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ondervoeding malnutrition

Interventions

Participants receive a high-protein diet: the experimental group receives extra (protein-rich) dairy products, and the control group receives extra oral nutrition supplements for in between use in o

Dairy products

Malnutrition

Oral nutrition supplements

Protein

Eligibility

Age

18 Years to 64 Years

Inclusion criteria

Inclusion criteria: * Risk for malnutrition (MUST = 0 or 1 point and PG-SGA SF score >= 4 and

Exclusion criteria

Exclusion criteria: * Use of oral nutrition supplements in the past six months at time of inclusion. * Receiving treatment of a dietician at time of inclusion. * High current daily protein intake (less than 12 gram difference between current intake and protein requirement). * Protein requirements >18 gram protein per day. * Prescription of oral nutrition supplements by the dietician. * Contra-indication for dairy products (e.g. lactose-intolerance, cow milk allergy). * Protein restriction ( 2 months ago); Duchenne muscular dystrophy; Gout. * Fluid restriction (6 months). * Eating disorder. * Dementia. * Distance from home to the UMCG is greater than 70 km. (due to practical reasons concerning distribution of the products).

Design outcomes

Primary

Measure	Time frame
The main study parameter is compliance, specified as adherence to prescription of daily protein goals (daily protein intake). A compliance questionnaire will be assessed to list the experiences of the participant about associated factors of compliance.	—

Secondary

Measure	Time frame
Secondary study parameters are (1) patient experiences (2) urine nitrogen secretion, (13) nutritional status, (24) body composition (BMI, bio-electrical impedance analysis), and (35) hand grip strength.	—

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)