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ID
Bron
Aandoening
Stroke, upper extremity function
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Main study parameters represent event-related gaze behaviour during the movement tasks, by calculating proportions of task duration with gaze focused on task-relevant objects (TRO gaze), on task-relevant body parts (TRB gaze), and on task-irrelevant objects (TIO gaze) (expressed in percentages of total task duration).
Achtergrond van het onderzoek
Objective: The primary objective is to gain insight into gaze behaviour of stroke survivors during active execution of upper extremity movements.
Study design: The current study is an observational study with one measurement session per participant.
Study population: In total, 20 stroke patients and 10 healthy subjects, with an age between 18-80 years old, will participate in this study.
Intervention (if applicable): Not applicable.
Main study parameters/endpoints: Main study parameters represent event-related gaze behaviour during the movement tasks, by calculating proportions of task duration with gaze focused on task-relevant objects (TRO gaze), on task-relevant body parts (TRB gaze), and on task-irrelevant objects (TIO gaze) (expressed in percentages of total task duration).
Doel van het onderzoek
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Onderzoeksopzet
The current study is an observational study with one measurement session per participant.
Onderzoeksproduct en/of interventie
GAze behavior is tracked during the following 3D tasks
Reach task
Reach and grasp of cylindrical object
Reach and replace of cylindrical object
Bimanual drinking task
Publiek
Roessingh Research and Development
Postbus 310
A.L. van Ommeren
Enschede 7500 AH
The Netherlands
a.vanommeren@rrd.nl
Wetenschappelijk
Roessingh Research and Development
Postbus 310
A.L. van Ommeren
Enschede 7500 AH
The Netherlands
a.vanommeren@rrd.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Patients should be clinically diagnosed with unilateral, either right or left sided, middle cerebral artery stroke (ischemic or hemorrhagic)
Between 18-80 years of age
Time since onset of disease is at least one week
Sufficient cognitive status to understand two-step instructions
Patients should be able to lift their affected arm on the table and to grasp a cylindrical object while seated in a chair
Provide written informed consent
Healthy subjects
Between 18-80 years of age
Sufficient cognitive status to understand two-step instructions
Provide written informed consent
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
People with severe acute pain of the (affected) arm and hand
People having insufficient knowledge of the Dutch language to understand the purpose or methods of the study
People with visual deficits; either ophthalmic (e.g. wearing glasses or lenses stronger than -5 or + 3) or cerebral
Severe contractures limiting passive range of motion in the UE
Co-morbidities limiting functional use of the arm and hand
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL6563 |
| NTR-old | NTR6744 |
| CCMO | NL59420.044.16 |
| OMON | NL-OMON45658 |