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Tele-stroke versus Stroke physician in Management of Acute Stroke

Smartphone based Telestroke Vs ‘Stroke Physician’ led Acute Stroke Management (SMART INDIA): A cluster randomised trial - SMART INDIA

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/11/038196
Enrollment
3652
Registered
2021-11-23
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: I60-I69- Cerebrovascular diseases

Interventions

Intervention1: Intervention 1: Tele-stroke based physician management: Intervention 1: The physicians of the district hospitals who get randomised to Telestroke arm will use smartphone based Telestrok

Sponsors

DHR ICMR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion criteria for unit of cluster (district hospital) 1. District hospitals where only non-stroke physicians are available 2. Physicians should have experience of using a smartphone with 24/7 internet access 3. Availability of CT scan Individual level 1. Age greater than or equal to 18 years 2. Diagnosis of acute Ischemic stroke ( 3. Provide written, informed consent to receive the intervention

Exclusion criteria

Exclusion criteria: Exclusion criteria for unit of cluster (district hospital) 1. Availability of a neurologist in the hospital 2. Lack of smart phone or internet access Individual level 1. Patients not with terminal illness 2. Not willing to give consent

Design outcomes

Primary

MeasureTime frame
The primary outcome will be the composite score (percentage) of performance of stroke care bundle. Highest score (100%) will be achieved if all the eligible patients received the standard stroke care bundle. 24 measures are grouped into 4 bundles (acute management, in-hospital management, Discharge advice, and follow up)Timepoint: 1 month and 3 months

Secondary

MeasureTime frame
Proportion of patients achieving mRS 0-2Timepoint: 1 month and 3 months;Proportion of patients who received Aspirin within 48 hrsTimepoint: 1 month and 3 months;Proportion of patients who received Dysphagia screening testTimepoint: 1 month and 3 months;Proportion of patients who received RehabilitationTimepoint: 1 month and 3 months;Proportion of patients who received Smoking cessation counsellingTimepoint: 1 month and 3 months;Proportion of patients who received statinsTimepoint: 1 month and 3 months;Proportion of patients who received Venous thromboembolism prophylaxisTimepoint: 1 month and 3 months;Proportion of patients who were evaluated for physiotherapy within 48 hrsTimepoint: 1 month and 3 months;Proportion of patients with AF who received AnticoagulantsTimepoint: 1 month and 3 months;Proportion of patients with newly diagnosed Atrial fibrillationTimepoint: 1 month and 3 months;Proportion of patients without AF who received antipalteletsTimepoint: 1 month and 3 months

Countries

India

Contacts

Public ContactM V Padma Srivastava

All India Institute of Medical Sciences, New Delhi

vasanthapadma123@gmail.com9868398261

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 12, 2026