Actively Recruiting
A New 360° Dual-task Based Protocol for the Pre-clinical In-hospital and At-home Rehabilitation of Elderly: DUAL-Rehab
Led by Istituto Auxologico Italiano · Updated on 2025-08-04
90
Participants Needed
1
Research Sites
144 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The main objective of this project is two-fold 1. to develop a Dual-Task training exploiting the potentiality of the 360° technology in terms of interactivity and ecological validity 2. to investigate its efficacy in improving the cognitive functioning in a randomized clinical trial for 2 different populations: subjects with subjective memory complaints and mild cognitive impairment. Specifically, participants will follow an integrated training including 2 phases: 1)in-hospital rehabilitation, where subjects will be provided sessions of the training in immersive modality; 2)at-home rehabilitation, where older adults will be asked to perform at home the non-immersive version of the training using a tablet. Expected outcome is an improvement in cognitive functioning (assessed with a complete neuropsychological battery) after the training, thus advancing literature about non-pharmacological interventions in the preclinical stages of dementia along with innovative technical instruments.
CONDITIONS
Official Title
A New 360° Dual-task Based Protocol for the Pre-clinical In-hospital and At-home Rehabilitation of Elderly: DUAL-Rehab
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 65 years
- Self-reported memory complaints (for the subjective memory complaint group)
- Mini-Mental State Examination score of 27 or higher (normal range) for the subjective memory complaint group
- Self-reported or caregiver-reported cognitive decline (for the mild cognitive impairment group)
- Objective cognitive impairment on neuropsychological testing for the mild cognitive impairment group
- Clinical Dementia Rating score less than 0.5
You will not qualify if you...
- No evidence of objective impairments on neuropsychological testing
- Clinical Dementia Rating score 0.5 or higher
- Diagnosis of dementia
AI-Screening
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Trial Site Locations
Total: 1 location
1
Istituto Auxologico Italiano IRCCS
Milan, MI, Italy, 20149
Actively Recruiting
Research Team
E
Elisa Pedroli, PsyD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
FACTORIAL
Primary Purpose
TREATMENT
Number of Arms
6
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