Actively Recruiting
Validation of a Digital Intervention to Rehabilitate Cognitive Resources
Led by Fondazione Don Carlo Gnocchi Onlus · Updated on 2026-02-13
102
Participants Needed
1
Research Sites
103 weeks
Total Duration
On this page
Sponsors
F
Fondazione Don Carlo Gnocchi Onlus
Lead Sponsor
U
Università Carlo Cattaneo , Castellanza
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn if the use of a digital cognitive rehabilitation system named RICORDO, that is flexible and capable of adapting the rehabilitation pathway according to the needs and capacity of the patients will prove effective for subjects with Subjective Memory Complaint or with Mild Cognitive Impairment or with Mild Dementia. The main questions it aims to answer are: Will the RICORDO rehabilitation treatment, lead to an improvement in the global cognitive level? Will the RICORDO rehabilitation treatment lead to improved activation of participants in managing their own health and healthcare? Researchers will compare the multidomain cognitive rehabilitation strategy of RICORDO digital solution, with a standard paper pencil rehabilitation care (usual care). Participants will undergo a comprehensive neuropsychological evaluation immediately before, immediately after and six months after the completion of the rehabilitation program. Both interventions, the experimental and the usual care, will last 5 weeks, with 3 weekly sessions of 45 minutes each and can be done autonomously by the patient at home.
CONDITIONS
Official Title
Validation of a Digital Intervention to Rehabilitate Cognitive Resources
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Montreal Cognitive Assessment (MoCA) score greater than 17.79
- Clinical Dementia Rating (CDR) Scale score less than or equal to 1
- Education level of more than 3 years
- Age 65 years or older
- Signed informed consent to participate
- Availability of a caregiver or study partner to support the participant
- Stable use of acetylcholinesterase inhibitors for the past 3 months, if applicable
You will not qualify if you...
- Presence of dysmetria or severe hearing, vision, or communication problems preventing participation
- Current rehabilitation program ongoing or within 3 months prior to enrollment
AI-Screening
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Trial Site Locations
Total: 1 location
1
IRCCS Fondazione Don Carlo Gnocchi ONLUS; Center of Advance Diagnostic and Therapy ( CADiTeR)
Milan, Italy, 20148
Actively Recruiting
Research Team
V
Valeria Blasi, MD
CONTACT
C
Chiara Pagliari, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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