Actively Recruiting
Resistance Training to Individuals for Cognitive Impairment With Dementia
Led by University of Beira Interior · Updated on 2024-08-06
80
Participants Needed
1
Research Sites
56 weeks
Total Duration
On this page
Sponsors
U
University of Beira Interior
Lead Sponsor
R
Research Center in Sports Sciences, Health Sciences and Human Development
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research project aims to analyze the effects of different resistance training volumes on cognitive function, oxidative stress, immunological response, lipid profile, glycemic status, liver function, muscle function, hemodynamic response, and physical performance in individuals with mild cognitive impairment. First the investigators will analyze the effects of a single resistance training session (acute effects) with one and three sets on hemodynamic and physical performance in individuals with mild cognitive impairment. After, the investigators will analyze the effects of an 8-week resistance training program with one or three sets on cognitive function, oxidative stress, immunological response, lipid profile, glycemic status, liver function, muscle function, hemodynamic response, and physical performance in individuals with mild cognitive impairment. The investigators hypothesize that a single resistance training session of one or three sets will increase the acute hemodynamic and physical performance stress in individuals with mild cognitive impairment, although with a higher magnitude in the session with three sets. Furthermore, we hypothesize that eight weeks of resistance training with one or three sets will induce similar improvements in cognitive function, oxidative stress, immunological response, lipid profile, glycemic status, liver function, muscle function, hemodynamic response, and physical performance in individuals with mild cognitive impairment.
CONDITIONS
Official Title
Resistance Training to Individuals for Cognitive Impairment With Dementia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Clinical diagnosis of mild cognitive impairment
- Short Physical Performance Battery (SPPB) score of 3 points or higher
- Willingness to participate in the interventions and collaborate with the research team
- Ability to provide informed consent (oral or written)
You will not qualify if you...
- Severe dementia
- Severe health conditions that affect participation in the intervention
- Color blindness
- Fractures within the last three months
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University of Beira Interior
Covilha, Portugal
Actively Recruiting
Research Team
N
Nuno Fonseca, Master's
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
FACTORIAL
Primary Purpose
PREVENTION
Number of Arms
5
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