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Clinical Trials/NCT02878304
NCT02878304
Unknown
Not Applicable

Recovery of Hand Function After Stroke- a Longitudinal Study Using Novel Methods to Quantify Hand Function and Connectivity in Brain Networks

Danderyd Hospital1 site in 1 country100 target enrollmentMarch 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
Danderyd Hospital
Enrollment
100
Locations
1
Primary Endpoint
Change in Fugl-Meyer Assessment for Upper Extremity
Last Updated
9 years ago

Overview

Brief Summary

The overall aim is to identify key determinants for recovery of hand function after stroke by applying newly developed hand function measures together with MRI measurements of the lesioned cerebral structures.

Detailed Description

Almost half of surviving stroke patients are left with impaired function of the hand but individual profiles of weakness, spasticity, sensory and bimanual function vary widely. Improved prediction of recovery after stroke has broad implications for clinical decisions on the type, duration and goals of rehabilitation. 100 consecutive patients with 1st ever stroke and upper limb hemi-paresis will be subject to imaging, at 4 weeks and 6 months, and behavioral assessments at 4 weeks, 3 months and 6 months after stroke. The imaging protocol includes anatomical sequences for lesion mapping, diffusion tensor imaging and resting-state functional MRI for structural and functional connectivity analyses, respectively. Clinical hand function measures will be combined with novel validated methods to quantify spasticity,grip force control, sensory and bimanual function. ProHand will provide insights into neural mechanisms related to recovery of hand function after stroke and enable enhanced prediction and development of targeted treatment trials.

Registry
clinicaltrials.gov
Start Date
March 2013
End Date
December 2017
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Danderyd Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • first ever stroke and clinically diagnosed arm paresis

Exclusion Criteria

  • incapability to give informed concent and/or understand and comply with instructions, other disorders that may affect hand function (e.g. other neurological conditions, arthritis), cerebellar lesions.

Outcomes

Primary Outcomes

Change in Fugl-Meyer Assessment for Upper Extremity

Time Frame: From 4 weeks to 3 and six months

Study Sites (1)

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