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Effect of Continued Nutritional Support at Hospital Discharge on Mortality, Frailty, Functional Outcomes and Recovery Trial: The EFFORT II Project

Status: Recruiting
Location: See all (18) locations...
Intervention Type: Other, Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study is to compare the sustained post-discharge nutritional support to reach individual energy and protein goals to usual care home nutrition in medical patients at nutritional risk.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Informed Consent as documented by signature

• Adult (age ≥18 years), medical patients

• Nutritional risk screening using the Nutritional Risk Screening (NRS): total score ≥3 points consisting of ≥1 points for impairment of the nutritional status \[weight loss \>5% in 3 month or food intake of 50-75% in the last week before hospital admission\] plus ≥1 for the severity of the disease (i.e., cancer, chronic kidney disease, chronic heart failure, COPD) and other chronic diseases according to the definition of the National Center for Chronic Disease Prevention and Health Promotion: Chronic diseases are defined broadly as conditions that last 1 year or more and require ongoing medical attention or limit activities of daily living or both .

Locations
Other Locations
Spain
Hospital Universitari Vall Hebron de Barcelona
RECRUITING
Barcelona
Hospital Universitario de Getafe
RECRUITING
Getafe
Complejo AComplejo Asistencial Universitario de León
RECRUITING
León
Hospital U. Gregorio Marañón de Madrid
RECRUITING
Madrid
Hospital Universitario Regional de Málaga
RECRUITING
Málaga
Hospital Clínico Universitario de Valladolid
RECRUITING
Valladolid
Switzerland
Kantonsspital Aarau, University Department of Internal Medicine
RECRUITING
Aarau
Bern University Hospital, Department of General Internal Medicine
COMPLETED
Bern
Spital Emmental Burgdorf
COMPLETED
Burgdorf
Spital Lachen
RECRUITING
Lachen
Kantonsspital Lucerne, Department of Internal Medicine
COMPLETED
Lucerne
Kantonsspital Münsterlingen
RECRUITING
Münsterlingen
Kantonsspital Sankt Gallen
COMPLETED
Sankt Gallen
Spital Thun
RECRUITING
Thun
Spital Zofingen
COMPLETED
Zofingen
Klinik Hirslanden Zürich
COMPLETED
Zurich
Stadtspital Zürich
COMPLETED
Zurich
Universitätsspital Zürich
COMPLETED
Zurich
Contact Information
Primary
Philipp Schuetz, Prof. Dr. med.
Philipp.Schuetz@unibas.ch
+41 (0) 62 838 9524
Time Frame
Start Date: 2021-08-05
Estimated Completion Date: 2026-12
Participants
Target number of participants: 1200
Treatments
Experimental: Intervention group: individualized nutritional support
Intervention group patients will receive individualized nutritional support to reach energy and protein goals with the support of an experienced, unblinded dietician and with use of oral nutritional supplements (ONS) as needed
Other: Control group: general information on healthy food habits
Control group patients will receive nutritional counselling (general information on healthy food habits) at discharge, but no nutritional support strategy will be used during follow-up
Related Therapeutic Areas
Sponsors
Leads: Philipp Schuetz

This content was sourced from clinicaltrials.gov

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