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Telemedicine Follow-up After Ischaemic Stroke: a Randomised Trial

BDCTR ID
BDCTR-2026-000127
Sponsor
Bangladesh Medical University
Information provided by
Dr Imran Chowdhury (Responsible Party)
Last Update Posted
2026-09-19

Recruiting

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Study Record Versions

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Viewing V1 (2026-09-19)

Study Details

Study Identification

Unique Protocol IDBMU-NEU-2026-004
Brief TitleTelemedicine Follow-up After Ischaemic Stroke: a Randomised Trial (TELE-STROKE)
Official TitleTelemedicine-supported Rehabilitation Follow-up Versus Standard In-person Care After Ischaemic Stroke
Secondary IDs

Study Status

Record Verification2026-09
Overall StatusRecruiting
Study Start2026-09-01
Primary Completion2027-05-31
Study Completion2027-08-31
First Submitted
First Submitted that Met QC Criteria2026-08-30
First Posted2026-08-30 [Actual]
Last Update Submitted that Met QC Criteria2026-09-19
Last Update Posted2026-09-19 [Actual]

Oversight

U.S. FDA-regulated Drug
U.S. FDA-regulated Device
Product manufactured in and exported from the U.S.
Data MonitoringNo

Study Description

Brief SummaryThis study compares telemedicine-supported rehabilitation follow-up with standard in-person care on functional recovery in the first 90 days after ischaemic stroke.
Detailed DescriptionPatients discharged after ischaemic stroke are randomised to telemedicine-supported follow-up or standard in-person rehabilitation. The primary endpoint is the modified Rankin Scale at 90 days.

Conditions

ConditionIschaemic Stroke Stroke Rehabilitation
Keywordsstroke telemedicine rehabilitation

Study Design

Study TypeInterventional
Primary PurposeSupportive Care
Study PhaseN/A
Interventional Study ModelParallel Assignment
Number of Arms2
MaskingSingle blind
AllocationRandomized
Enrollment320 [Estimated]

Arms and Interventions

ArmsAssigned Interventions
Experimental: Telemedicine follow-upBehavioral: Telemedicine-based rehabilitation follow-up Scheduled video consultations with a rehabilitation team.
Active Comparator: Standard in-person care

Outcome Measures

Primary Outcome MeasuresModified Rankin Scale score Time Frame: 90 days
Secondary Outcome MeasuresBarthel Index Time Frame: 90 days

Eligibility

Minimum Age40 Years
Maximum Age80 Years
Ages40 Years to 80 Years (Adult, Older Adult)
SexAll
Gender-based Eligibility
Gender Eligibility Description
Accepts Healthy VolunteersNo
Criteria<p>Inclusion Criteria:</p><ul><li>Adults aged 40 to 80 years with confirmed ischaemic stroke.</li><li>Access to a mobile phone.</li></ul><p>Exclusion Criteria:</p><ul><li>Severe cognitive impairment preventing participation.</li></ul>

Contacts/Locations

Central Contact PersonDr Imran Chowdhury +8802550000127 stroke-tele@bmu.ac.bd
Study Officials
LocationDhaka, Dhaka, Bangladesh, 1000 Status: Recruiting Facility: Bangladesh Medical University, Department of Neurology

IPD Sharing

IPD informationPlan to Share IPD: Not provided

References

Citations
Links
Available IPD/Information

Document Section

Documents