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Study identifier: NCT06429215 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

REducing the Risk of COgnitive DEcline ad Dementia in Patients With Subjective Cognitive Decline Through an Immersive Virtual Reality and Telemedicine-based Multi-component Intervention: the SCD-ReCODED Study

Condition: Subjective Cognitive Decline  ·  Sponsor: I.R.C.C.S. Fondazione Santa Lucia

PhaseNA
Planned participants75
Who can joinAll sexes, 55 Years to 80 Years
Healthy volunteersYes

About this study

Older adults with subjective cognitive decline (SCD) are at high risk of developing dementia and frequently experience subclinical symptoms (e.g., anxiety, depression) which are themselves associated with dementia and cognitive decline risk. To date, the lack of effective disease-modifying treatments, along with the reliable identification of modifiable lifestyle risk factors (e.g., cognitive activity, dietary habits, physical exercise), have led to growing interest to invest in non-pharmacological interventions that may reduce the prevalence and incidence of dementia and cognitive decline in older adults. In this framework, the aim of this project is to evaluate the efficacy of an Immersive Virtual Reality (IVR) and telemedicine-based multi-component intervention, combining cognitive training and a health and lifestyle education program, for preventing cognitive decline and dementia in at-risk individuals (i.e., SCD). For this purpose, a randomized, double-blinded controlled trial (RCT) will be conducted on seventy-five eligible individuals with SCD, who will be randomly assigned to one of three conditions: (a) multi-component intervention (MC-I), including SCD-tailored cognitive IVR training plus a health and lifestyle education program, (b) cognitive-only intervention (CO-I), including the SCD-tailored cognitive IVR training plus an active control for the education program, and (c) active control intervention (AC-I) for both cognitive training and education program. Interv…

This description comes directly from the study's public registry record.

Talk to the study team

Maria Stefania De Simone, Dr  ·  (+39) 06-51501189  ·  ms.desimone@hsantalucia.it

Always discuss trial participation with your own doctor first.

Locations (1)

I.R.C.C.S Santa Lucia FoundationRome, Lazio, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06429215