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Study of Sensory Deficits in the Upper Limb After Stroke

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01685788
Enrollment
40
Registered
2012-09-14
Start date
2012-10-31
Completion date
2015-03-31
Last updated
2016-10-26

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

Conditions

Stroke

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.

Interventions

OTHERNo intervention

Sponsors

KU Leuven
CollaboratorOTHER
Universitaire Ziekenhuizen KU Leuven
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frame
Change in sensory function in upper limb from baseline up to 6 months post stroke6 months post stroke

Secondary

MeasureTime frame
Change in motor function in upper limb from baseline up to 6 months post stroke6 months post stroke

Other

MeasureTime frameDescription
activity measure6 months post strokeThe investigators will use the ABILHAND Questionnaire, a measure of how well the hemiplegic arm and hand can be used in daily activities.
Activity measure6 months after strokeThe Assisting Hand Assessment (AHA) will be used to investigate the use of the hemiplegic arm in bimanual tasks after stroke.
Participation measure6 months after strokeThe quality of life will be measured using the Stroke Impact Scale.

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026