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Development and validation of a Software to enhance mental functions in Older Adults

Development and validation of a Software BoostMem to enhance Cognitive Reserve in Older Adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064244
Enrollment
120
Registered
2024-03-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: F015- Vascular dementia

Interventions

Intervention1: Non-randomized, Active Controlled Trial: 30 Dementia patients Control Intervention1: Healthy older adults and Young adults: 30 cognitively normal older adults, and 60 individuals aged b

Sponsors

DST
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The study would include 30 dementia patients, 30 cognitively normal older adults, and 60 individuals aged between 45 and 64 years.

Exclusion criteria

Exclusion criteria: Denial of Consent

Design outcomes

Primary

MeasureTime frame
This is a unique study to develop and test the effectiveness, feasibility and acceptability of an indigenously developed software ‘BoostMem’ in treating and preventing cognitive impairment among older adults.Timepoint: 36 months—

Secondary

MeasureTime frame
To prevent and diagnose cognitive impairment in older peopleTimepoint: 36 months—

Countries

India

Contacts

Public ContactDr Prasun Chatterjee

AIIMS Delhi

drprasun.geriatrics@gmail.com01126546072

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026