A new dual-task rehabilitation program for elderly cognitive decline
A New 360° Dual-task Based Protocol for the Pre-clinical In-hospital and At-home Rehabilitation of Elderly: DUAL-Rehab
This study is testing a new training program using virtual reality to see if it can help older adults with memory issues and mild cognitive impairment think better.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 90 (estimated) |
| Ages | 65 Years and up |
| Sex | All |
| Sponsor | Istituto Auxologico Italiano Academic / other |
| Locations | 1 site (Milan, MI) |
| Trial ID | NCT06290167 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates are individuals over 65 years old with self-reported memory complaints or mild cognitive impairment.
Not a fit: Patients with no evidence of cognitive decline or dementia may not benefit from this intervention.
Why it matters
Potential benefit: If successful, this program could significantly enhance cognitive functioning in elderly patients at risk of dementia.
How similar studies have performed: While similar approaches have been explored, this specific use of 360° technology in dual-task training for cognitive rehabilitation is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
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 this trial is running
Milan, MI
- Istituto Auxologico Italiano IRCCS — Milan, Mi, Italy (Recruiting)
Study contacts
- Study coordinator: Elisa Pedroli, PsyD
- Email: e.pedroli@auxologico.it
- Phone: 02 61911 2707
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.