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Clinical Trials/NCT06569771
NCT06569771RecruitingNot Applicable

Evolution of the Patient's Perception of the Use of the Upper Limb After a Stroke During Intensive Rehabilitation

Grand Hôpital de Charleroi4 sites in 1 country100 target enrollmentStarted: June 11, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
100
Locations
4
Primary Endpoint
To assess whether the perception of use of the impaired upper limb improves during intensive rehabilitation after a stroke.

Study Overview

Brief Summary

This study is being carried out in the context of rehabilitation after stroke, where persistent upper limb weakness is a major challenge. It aims to explore the relationship between observed function and patients' perceived participation in use.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • First stroke as defined by the World Health Organization.
  • Upper limb paresis with a NIHSS National Institutes of Health Stroke Scale score > or = 1/4 for upper limb motor function

Exclusion Criteria

  • Life expectancy <12 months
  • Inability to understand French.
  • Pre-existing severe multiple disability affecting arm function.
  • Presence of pre-existing central neurological pathologies.
  • Mini-Mental State Examination < 21

Arms & Interventions

Patients suffering from motor impairment of the upper limbs following a stroke

Voluntary patients suffering from motor impairment of the upper limbs following a stroke

Intervention: Functional assessments (Diagnostic Test)

Outcomes

Primary Outcomes

To assess whether the perception of use of the impaired upper limb improves during intensive rehabilitation after a stroke.

Time Frame: Up to 2 months

various tests : computer adaptive test F-M, ARA test, MIF test, star concellation test, ACTIVLIM test

To compare the difference between perception and observed function of the upper limb during intensive multidisciplinary rehabilitation treatment.

Time Frame: Up to 2 months

various tests : computer adaptive test F-M, ARA test, MIF test, star concellation test, ACTIVLIM test

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Grand Hôpital de Charleroi
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (4)

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