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Clinical Trials/NCT01685788
NCT01685788
Completed
N/A

Prospective Longitudinal Study: Sensory Deficits in the Upper Limb After Stroke.

Universitaire Ziekenhuizen KU Leuven1 site in 1 country40 target enrollmentOctober 2012
ConditionsStroke

Overview

Phase
N/A
Intervention
Not specified
Conditions
Stroke
Sponsor
Universitaire Ziekenhuizen KU Leuven
Enrollment
40
Locations
1
Primary Endpoint
Change in sensory function in upper limb from baseline up to 6 months post stroke
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The overall aim of the project is to gain insight in sensory deficits and recovery patterns in the upper limb post stroke and its association with brain lesion localisation. Furthermore, the investigators will identify associations of deficits in sensory modalities with upper limb impairments, activities and participation at different time points after stroke. Identification of the sensory deficits, along with further insights in their relation with objective neurophysiological and neuroanatomical measures will contribute to the amelioration of goal-setting for the rehabilitation of upper extremity function after stroke. These functions are indispensable during several daily activities as well in different sports and leisure activities. This project is an important step towards a better delineating of treatment interventions for the upper limb and to a better guiding of individual needs for post-stroke treatment in the future.

Registry
clinicaltrials.gov
Start Date
October 2012
End Date
March 2015
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sarah Meyer

PhD Student

Universitaire Ziekenhuizen KU Leuven

Eligibility Criteria

Inclusion Criteria

  • first-ever stroke as defined by WHO
  • ≤ 5 days post stroke
  • motor impairment and/or a sensory impairment
  • ≥ 18 years old
  • sufficient cooperation to execute evaluations

Exclusion Criteria

  • other neurological impairments such as previous stroke, head injury or multiple sclerosis (these might affect sensory ability independently of the stroke)
  • stroke-like symptoms caused by subdural hematoma, tumour, encephalitis or trauma
  • no informed consent
  • pre-stroke Barthel Index \< 95 out of 100 points (to be able to distinguish between pre-existing disabilities and disabilities resulting from the stroke)

Outcomes

Primary Outcomes

Change in sensory function in upper limb from baseline up to 6 months post stroke

Time Frame: 6 months post stroke

Secondary Outcomes

  • Change in motor function in upper limb from baseline up to 6 months post stroke(6 months post stroke)

Study Sites (1)

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