Tracking of Upper Limb Sensory and Motor Recovery in Asian Stroke Survivors
NCT ID: NCT05322837
Last Updated: 2025-04-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
400 participants
OBSERVATIONAL
2023-04-26
2026-01-31
Brief Summary
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Hence, this study aims to better understand upper limb recovery covering different stages post-stroke in a representative cohort of Asian adults
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Detailed Description
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The aim of this longitudinal and observational study is to gather a rich multi-modal database on the time-course of upper limb recovery in a representative cohort after stroke and characterise the relationship between upper limb recovery, common post-stroke impairments and quality of life.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Intervention
Clinical and technological-aided assessments and questionnaires
Assessments and questionnaires related to upper limb function and quality of life will be used
Interventions
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Clinical and technological-aided assessments and questionnaires
Assessments and questionnaires related to upper limb function and quality of life will be used
Eligibility Criteria
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Inclusion Criteria
2. First ever confirmed stroke
3. Asian ethnicity
4. Age 21-90 years
5. Montreal Cognitive Assessment (MOCA) scores 21/30 and above
6. Admission to rehabilitation ward is within 8 weeks of stroke onset
Exclusion Criteria
2. Upper limb impairment not related to stroke: e.g., subarachnoid haemorrhage, traumatic brain injury or brain tumours
3. Bilateral upper limb impairment.
4. Uncontrolled medical conditions such as hypertension, hypotension, diabetes mellitus, unstable angina, cardiac failure or sepsis will be excluded.
5. Active fractures or arthritis of upper limb joints/bones
6. Visual Analogue Scale (VAS) pain \> 5/10
7. MOCA \< 21/30
8. Severe behavioural disturbance or agitation or epilepsy or untreated depression
9. Life expectancy \< 6 months
10. End organ failures on replacements (renal dialysis or renal replacement therapies)
11. Minimally responsive or unresponsive awareness (vegetative) states
12. Pregnancy or lactation states
13. Admission to rehab ward later than 8 weeks post-stroke
14. (For TMS assessments only) History of epilepsy or seizures, or cranial surgeries, or have metal implants in body or head, or have implanted electronics, or have metallic valve, or skull fracture or brain injury, or head or brain surgeries.
21 Years
90 Years
ALL
No
Sponsors
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Rehabilitation Research Institute of Singapore (RRIS)
UNKNOWN
Singapore-ETH Centre (SEC)
UNKNOWN
Tan Tock Seng Hospital
OTHER
Responsible Party
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Principal Investigators
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Dr Karen Chua, MBBS
Role: PRINCIPAL_INVESTIGATOR
Tan Tock Seng Hospital
Locations
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Tan Tock Seng Hospital
Singapore, , Singapore
Countries
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Central Contacts
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Facility Contacts
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References
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Cheng HJ, Chin LF, Kanzler CM, Lehner R, Kuah CWK, Kager S, Josse E, Samkharadze T, Sidarta A, Gonzalez PC, Lie E, Zbytniewska-Megret M, Wee SK, Liang P, Gassert R, Chua K, Lambercy O, Wenderoth N. Upper limb sensorimotor recovery in Asian stroke survivors: a study protocol for the development and implementation of a Technology-Assisted dIgitaL biOmaRker (TAILOR) platform. Front Neurol. 2023 Nov 30;14:1246888. doi: 10.3389/fneur.2023.1246888. eCollection 2023.
Other Identifiers
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DSRB 2021/00919
Identifier Type: -
Identifier Source: org_study_id
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