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Clinical Trials/DRKS00012273
DRKS00012273
Recruiting
未知

Prevention of malnutrition and sarcopenia in aging people with proteindrinks

ehrstuhl für Ernährungsmedizin der Technischen Universität München0 sites80 target enrollmentMay 24, 2017

Overview

Phase
未知
Intervention
Not specified
Conditions
Acceptance of a protein drink of older people that was designed regarding the physiological requirements and taste preferences of older people. Effect of the regular consumption of the drink on protein intake and dietary habits.
Sponsor
ehrstuhl für Ernährungsmedizin der Technischen Universität München
Enrollment
80
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 24, 2017
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
ehrstuhl für Ernährungsmedizin der Technischen Universität München

Eligibility Criteria

Inclusion Criteria

  • 75 \- 85 years, willingness to participate, no guardianship, live in private household, able to get to the study centre, caucasian

Exclusion Criteria

  • current participation in an intervention study, smoker, chronic infection, chronic liver disease,
  • diagnosed diabetes mellitus, untreatet endocrine disease, diagnosed autoimmune disease, diagnosed myocardial infarction within the last 3 years, diagnosed stroke within the last 3 years, pacemaker, untreatet hypertension \>150/95 mmHg, diagnosed coronary cardiopathy within the last 3 years, cancer within the last 3 years, kidney disease requiring dialysis, Parkinson disease, liver disease, stomach ulcer, chronic lung disease with oxygen supply, circulatory disorder in the legs, diagnosed mental illness or neuroleptic desease within the last 3 years, immobile (chairbound), nursing case, unintentionally loss in weight \>5% in the last 3 month, blood transfusion in the last 3 month, lactose intolerance, fructose intolerance, milk protein allergy, allergy against seafood, fish or crustaceans, vegan or vegetarian diet

Outcomes

Primary Outcomes

Not specified

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