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Telerehabilitation versus in clinic computerized cognitive training on community dwelling stroke survivors

Evaluation of comparative efficacy of telerehabilitation versus In clinic computerized cognitive training on cognition daily Function and adherence in community dwelling stroke survivors a randomized controlled trial - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/083722
Enrollment
52
Registered
2025-03-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: G998- Other specified disorders of nervous system in diseases classified elsewhere Health Condition 2: G998- Other specified disorders of nervous system in diseases classified elsewhere

Interventions

Intervention1: Telerehabilitation Cognitive Training: Session will be conducted online for 30 mins by using various tools available at their places It will last for 5 days weekly with for 2 weeks to 6

Sponsors

Ravi Nair Physiotherapy College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Subjects diagnosed with stroke by a clinician confirmed by radiodiagnosis with a duration of 3 months following a stroke between 45 to 65 years of age 2 The primary caregiver of the stroke survivors must also be consistent with participants in this study 3 The primary caregiver or the stroke subject must be using an Android or an iOS-based smartphone 4 The subjects must have a cognitive behavioural score less than 24 in MMSE or MOCA 5 The subject must have modified dependence with of less than 75 to 100 % and with a modified independence relying on the device

Exclusion criteria

Exclusion criteria: 1 Stroke in young 2 Multiple or recurrent strokes 3 The subjects with cardiac pacemakers or implants and other relevant devices 4 The subjects with severe spasticity hindering ADLs or bed mobility 5 Subjects with moderate to severe cognition impairment 6 Subjects with severe trunk impairment 7 Subject with any type of pain 8 Subject with a history of trauma requiring medicines or surgical management 9 Subject without caregiver 10 Subject living in old age homes or assisted living 11 Subjects who are under medications like intrathecal or epidural pump or botulinum

Design outcomes

Primary

MeasureTime frame
Montreal Cognitive Assessment MoCA Digit Span TestTimepoint: Baseline 2 weeks 4 weeks 3 months

Secondary

MeasureTime frame
Stroke Specific Quality of Life Scale SS-QOL Stroke Impact Scale SISTimepoint: Baseline 2 weeks 4 weeks 3 months

Countries

India

Contacts

Public ContactHarshada Awachat

Ravi Nair Physiotherapy College

raghuneuro@yahoo.com8126506769

Outcome results

None listed

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