Actively Recruiting

Phase Not Applicable
Age: 75Years +
All Genders
NCT07067697

Impact of Physical Exercise on Hospitalized Older Adults Malnourished or at Risk, With Oral Nutritional Support

Led by Fundacion Miguel Servet · Updated on 2025-09-24

102

Participants Needed

1

Research Sites

50 weeks

Total Duration

On this page

Sponsors

F

Fundacion Miguel Servet

Lead Sponsor

N

Nestle Health Science

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim of this research is to analyze whether nutritional intervention combined with a multicomponent physical training program based on strength, balance, and aerobic exercises can prevent disability caused during hospitalization in individuals aged 75 years or older admitted for medical conditions, thereby improving functional and cognitive capacity. To achieve this objective, we will conduct a randomized clinical trial in which patients are randomly assigned to either the control group, which does not perform the physical training, or the intervention group, which participates in the multicomponent physical training program.

CONDITIONS

Official Title

Impact of Physical Exercise on Hospitalized Older Adults Malnourished or at Risk, With Oral Nutritional Support

Who Can Participate

Age: 75Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 75 years or above
  • Hospitalized in the Acute Unit of the Geriatrics Service at the University Hospital of Navarra
  • Expected hospitalization of 4 days or more
  • Malnourished according to GLIM criteria or at risk of malnourishment (MUST scale)
  • Barthel Index of 60 points or higher
  • Able to tolerate oral intake
  • Able to walk with or without assistance
  • Able to understand instructions and communicate
  • Provide informed consent (participant or legal guardian)
Not Eligible

You will not qualify if you...

  • Advanced major neurocognitive disorder (GDS 6 and 7)
  • Uncontrolled cardiac arrhythmia, acute pulmonary thromboembolism, acute myocardial infarction, or bone fractures within the last 3 months
  • Chronic kidney disease stage 4 or 5
  • Safe and effective swallowing only with pudding texture
  • Physical limitations preventing participation in the exercise program
  • Participation in another study that may interfere with data or participation in another study within the past 6 months

AI-Screening

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Trial Site Locations

Total: 1 location

1

University Hospital of Navarra

Pamplona, Navarre, Spain, 31008

Actively Recruiting

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Research Team

C

Chenhui Chen, Doctor

CONTACT

N

Nicolás Martínez Velilla, Doctor, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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