A new dual-task rehabilitation program for elderly cognitive decline

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project aims to develop a dual-task training protocol utilizing 360° technology to enhance interactivity and ecological validity for elderly patients. The study will assess its efficacy in improving cognitive functioning among two groups: individuals with subjective memory complaints and those with mild cognitive impairment. Participants will undergo a two-phase rehabilitation process, starting with immersive in-hospital sessions followed by at-home training using a tablet. The expected outcome is improved cognitive functioning, evaluated through a comprehensive neuropsychological assessment.

Why it matters

Who can join: the full rules

Inclusion Criteria (group of SMC):

* \> 65 years old
* self-reported memory complaints
* score on Mini-Mental State Examination greater than or equal to 27/30 (normal range)

Exclusion Criteria:

* no evidence of objective impairments on the neuropsychological testing, scores on the Clinical Dementia Rating \< 0.5

Inclusion Criteria (group of MCI):

* \> 65 years old
* a self-reported (or reported by a caregiver) cognitive decline
* an objective impairment on the neuropsychological testing
* scores on the Clinical Dementia Rating \< 0.5.

Exclusion Criteria:

* no dementia

Where it's running

• Istituto Auxologico Italiano IRCCS
  Milan, Mi, Italy Recruiting

Study contacts

• Study coordinator: Elisa Pedroli, PsyD
• Email: e.pedroli@auxologico.it
• Phone: 02 61911 2707

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.