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Using MRI to detect somatosensory deficiency in early sub-acute stroke: the key to predicting recovery of arm-hand capacity?

Using MRI to detect somatosensory deficiency in early sub-acute stroke: the key to predicting recovery of arm-hand capacity? - MRI based detection of somatosensory deficiency in stroke

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON55345
Enrollment
20
Registered
2021-04-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

cerebrovascular accident (CVA) stroke

Interventions

None listed

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Early sub-acute ischemic or hemorrhagic stroke (2 weeks post-stroke) 2. First ever stroke 3. Diagnosed with moderate to severe unilateral arm-hand motor impairments (Fugl-Meyer Upper Extremity score

Exclusion criteria

Exclusion criteria: 1. Non-stroke related somatosensory and motor co-morbidity that may interfere with arm-hand function 2. Bilateral motor impairments 3. MRI contraindications (pacemaker, claustrophobia, vein clip, pregnancy, etc.) 4. Not able to understand or sign informed consent 5. Severe cognitive impairments and/or aphasia that interfere with the patient's ability to read or understand the study instructions

Design outcomes

Primary

MeasureTime frame
The Action Research Arm Test (ARAT) will be used to assess patients* arm-hand skill performance capacity. Functional MRI will be used to assess the size of the functional finger representation in the primary somatosensory cortex. Diffusion MRI will be used to assess the integrity of somatosensory and motor white matter fiber tracts within the brain.

Secondary

MeasureTime frame
n.a.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)