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APP Based Cognitive Retraining in Mild Cognitive Impairment

Digital Cognitive Augmentation Programme (D-CAP) in Mild Cognitive Impairment: A Feasibiltiy RCT Study - JES

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/041605
Enrollment
60
Registered
2022-04-04
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: F01-F99- Mental, Behavioral and Neurodevelopmental disorders

Interventions

Intervention1: App based Cognitive retraining (D-CAP): After the pre assessment the patients will be randomly allocated to either the app based cognitive retraining group or the treatment as usual gro

Sponsors

UGC JRF
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) fulfilling DSM-V criteria for Mild neurocogntive disorder 2)clinical diagnosis made by psychiatrist or neurologist 3)access to smartphone 4)able to read, write and compute 5) right hand dominance 6)normal corrected vision/hearing 7)fluecny in either english, malayalam, Kannada, Tamil

Exclusion criteria

Exclusion criteria: 1)Presence or history of any psychiatric or neurological conditions. 2)Presence or history of substance abuse except for nicotine substance abuse. 3)History of intellectal disability . 4)Any chronic debilitating medical conditions. 5)Those who had recieved any form of cognitive/psychological interventions for last 6 months. 6)Severe sensorimotor deficits making them not amenable for testing.

Design outcomes

Primary

MeasureTime frame
neuropsychological functions such as attenion, fluency, working memory, visual memory, verbal memory and visuospatial construction.Timepoint: 1)baseline 2)6 weeks after the first intervention 3)6 weeks after the second intervention 4)6 months after the whole intervention

Secondary

MeasureTime frame
1)Quality of life (QOL), 2)Activities of daily living(ADL) , 3)Behavioral and psychological symptoms of dementia (BPSD)Timepoint: 1)baseline 2)6 weeks after the first intervention 3)6 weeks after the second intervention 4)6 months after the intervention

Countries

India

Contacts

Public ContactAmala Paul

Professor

keshavjkapp@gmail.com9900032852

Outcome results

None listed

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