Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
NCT06290167

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

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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

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Istituto Auxologico Italiano IRCCS

Milan, MI, Italy, 20149

Actively Recruiting

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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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