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Nutritional Therapy in Patients at Risk for Malnutrition and Sarcopenia in Pulmonary Rehabilitation

Primary Purpose

Sarcopenia, Malnutrition

Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
individual nutritional therapy
Sponsored by
Thimo Marcin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Sarcopenia focused on measuring individual nutrition therapy

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • admission to rehab due to chronic obstructive pulmonary disease or after a pneumonia
  • light to moderate risk of malnutrition (Nutritional Risk Score-2002: 3-4 Points)
  • risk of sarcopenia (sarc-f >=4)
  • signed informed consent

Exclusion Criteria:

  • medically described nutritional support
  • reasons (cognitive, language) that prevent a informed consent
  • enteral or parenteral nutrition
  • after bariatric surgery

Sites / Locations

  • Berner Reha ZentrumRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

individual nutrition therapy

usual care

Arm Description

Individualized nutrition therapy: Specialists in nutritional counseling determine the patient's individual energy and protein needs and create targeted individual measures to achieve them. Measures can include, for example, adjustments to the menu, food enrichment or supplementation. The measures are discussed with the patients on an ongoing basis and adjusted as necessary.

Usual care: Participants in the control group receive a standardized food fortification of the soups with fat and protein, as well as an energy- and protein-rich dessert. No additional advice or adjustments are made by the iNT.

Outcomes

Primary Outcome Measures

Energy intake
Change in energy intake [kcal] from start to end of rehabilitation.

Secondary Outcome Measures

protein intake
Change in protein intake [g] from start to end of rehabilitation.
grip strength
Change in grip strength (muscle strength) from start to end of rehabilitation.
lean body mass
Change in lean body mass (muscle mass) from start to end of rehabilitation.
time up and go
Change in time up an go time (muscle function) from start to end of rehabilitation

Full Information

First Posted
October 5, 2021
Last Updated
July 11, 2023
Sponsor
Thimo Marcin
Collaborators
Bern University of Applied Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT05096013
Brief Title
Nutritional Therapy in Patients at Risk for Malnutrition and Sarcopenia in Pulmonary Rehabilitation
Official Title
Effect of Individual Nutritional Therapy in Patients at Risk for Malnutrition and Sarcopenia in Pulmonary Rehabilitation - a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 16, 2021 (Actual)
Primary Completion Date
December 20, 2023 (Anticipated)
Study Completion Date
December 20, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Thimo Marcin
Collaborators
Bern University of Applied Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Malnutrition and sarcopenia (muscle wasting) are common in health care settings and represent a health and economic burden due to associated increased mortality and prolonged hospital stays. Nutritional therapy co-management is recommended for both diagnoses. This study investigates the efficacy of individualized nutrition therapy (iNT) in pulmonary rehabilitation. Patients at significant risk for malnutrition already receive iNT within clinical routine during rehabilitation. The investigators will investigate if patients with only mild to moderate risk of malnutrition and possible sarcopenia also benefit from iNT.
Detailed Description
The participating patients are randomly assigned to two groups after giving written consent. The intervention group receives individual counseling by nutrition therapists twice a week in addition to the usual rehabilitation program. The iNT determines the energy and protein needs of the patients and creates targeted individual measures to achieve them. Measures may include, for example, adjustments to the meal plan or nutritional supplementation. The measures are continuously adapted to the patients' needs. The control group also receives soup fortified with a standard amount of protein and fat and, if needed, an energy- and protein-rich dessert option as part of the rehabilitation routine care for patients at risk for malnutrition. However, patients from the control group do not receive additional counseling or adjustment by the iNT. Patients' energy and protein intake will be recorded on three subsequent days at start of rehabilitation and at three subsequent days before discharge. Average duration of rehabilitation is expected to be three weeks. As primary outcome, change in energy intake will be compared between groups. Additionally, change in protein intake and other follow-up parameters of nutritional status and sarcopenia will be examined.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sarcopenia, Malnutrition
Keywords
individual nutrition therapy

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Masking Description
Patients cannot be blinded due to the nature of the intervention. However, the personnel involved will be blinded to the collection of the primary endpoint. In order to be able to blind the nutritional calculations of the primary endpoint, the logged amounts of food eaten will be recorded on the neutral eating cards, on which the study group allocation will not be apparent.
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
individual nutrition therapy
Arm Type
Experimental
Arm Description
Individualized nutrition therapy: Specialists in nutritional counseling determine the patient's individual energy and protein needs and create targeted individual measures to achieve them. Measures can include, for example, adjustments to the menu, food enrichment or supplementation. The measures are discussed with the patients on an ongoing basis and adjusted as necessary.
Arm Title
usual care
Arm Type
No Intervention
Arm Description
Usual care: Participants in the control group receive a standardized food fortification of the soups with fat and protein, as well as an energy- and protein-rich dessert. No additional advice or adjustments are made by the iNT.
Intervention Type
Other
Intervention Name(s)
individual nutritional therapy
Intervention Description
Intervention arm: Usual care + individualized nutritional therapy. Patients at risk for malnutrition and sarcopenia will receive a counselling by the nutritional therapist twice a week. The therapists will assess the patient's energy and protein demand in order to develope appropriate individual measures (e.g additional meals or supplements) to increase patients' energy and protein intake. Individual nutritional therapy is already usual care in patients with high risk for malnutrition, but not for patients with only light to moderate risk of malnutrition and risk of sarcopenia.
Primary Outcome Measure Information:
Title
Energy intake
Description
Change in energy intake [kcal] from start to end of rehabilitation.
Time Frame
From admission to discharge (2-3 weeks)
Secondary Outcome Measure Information:
Title
protein intake
Description
Change in protein intake [g] from start to end of rehabilitation.
Time Frame
From admission to discharge (2-3 weeks)
Title
grip strength
Description
Change in grip strength (muscle strength) from start to end of rehabilitation.
Time Frame
From admission to discharge (2-3 weeks)
Title
lean body mass
Description
Change in lean body mass (muscle mass) from start to end of rehabilitation.
Time Frame
From admission to discharge (2-3 weeks)
Title
time up and go
Description
Change in time up an go time (muscle function) from start to end of rehabilitation
Time Frame
From admission to discharge (2-3 weeks)

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: admission to rehab due to chronic obstructive pulmonary disease or after a pneumonia light to moderate risk of malnutrition (Nutritional Risk Score-2002: 3-4 Points) risk of sarcopenia (sarc-f >=4) signed informed consent Exclusion Criteria: medically described nutritional support reasons (cognitive, language) that prevent a informed consent enteral or parenteral nutrition after bariatric surgery
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Thimo Marcin, PhD
Phone
+41 33 244 30 48
Email
t.marcin@rehabern.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Undine Lehmann, Dr
Phone
+41 31 848 47 56
Email
undine.lehmann@bfh.ch
Facility Information:
Facility Name
Berner Reha Zentrum
City
Heiligenschwendi
State/Province
Bern
ZIP/Postal Code
3625
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Thimo Marcin, PhD
Phone
+41 33 244 30 48
Email
t.marcin@rehabern.ch
First Name & Middle Initial & Last Name & Degree
Andrea Zurfluh, BSc
Phone
+41 33 244 34 50
Email
a.zurfluh@rehabern.ch

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data that underlie the results reported in this article, after deidentification (text, tables, figures, and appendices).
IPD Sharing Time Frame
2022, July

Learn more about this trial

Nutritional Therapy in Patients at Risk for Malnutrition and Sarcopenia in Pulmonary Rehabilitation

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