Effectiveness of Rehabilitation on the Recovery of Patients Post Right Stroke With Unilateral Spatial Neglect
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|ClinicalTrials.gov Identifier: NCT00305513|
Recruitment Status : Unknown
Verified March 2006 by Hadassah Medical Organization.
Recruitment status was: Not yet recruiting
First Posted : March 22, 2006
Last Update Posted : June 3, 2010
Unilateral spatial neglect (USN) is believed to be a disorder of attention, characterized by impairment in the ability to perceive or respond to stimuli presented to the contralesional space, and which is not attributable to significant sensory or motor deficits. USN has serious consequences for rehabilitation and long term disabilities. Efforts have been made to clarify both the theoretical basis of this phenomenon and the rehabilitation methods that will be best in improving function. The purpose of this study is to try and contribute to both efforts by examining treatment effectiveness of two methods; one targeting general arousal (phasic alerting), and the other targeting increasing awareness to left side stimuli and habit changes. Functional neuroimaging methods (PET [positron emission tomography] and fMRI [functional magnetic resonance imaging]) have been applied to understand the functional anatomy of the brain during mental processes. Only a few attempts have been made to use functional neuroimaging in patients with neurological deficits such as USN, usually speculations are made based on findings with healthy participants to explain this disorder. This study's aim is to examine the functional reorganization of the attentional network in the brain of USN patients while performing visual tasks, by means of functional neuroimaging techniques, in light of specific rehabilitation techniques.
Patients will be examined before and after 3 weeks of rehabilitation both using standardized neurobehavioral tests and PET imaging procedures.
|Condition or disease||Intervention/treatment||Phase|
|Cerebrovascular Accident Perceptual Disorders||Procedure: The phasic alerting treatment||Phase 2|
- first time right hemispheric stroke (ischemic);
- 2-6 weeks post stroke incident;
- ages 25-85;
- right hand dominance;
- minimum education of 6 years;
- do not suffer from field cut deficit such as hemi-anopsia;
- without other known neurological disorders (e.g., Parkinson's disease, aphasia);
- without severe systemic conditions (e.g., malignancies, AIDS, congestive heart failure, substance abuse);
- did not take additional medications that could affect the central nervous system; without dementia;
- without mental illness;
- the patients or their legal guardians have to give informed consent.
- six patients will be recruited and randomly allocated to one of the treatment groups (phasic alerting or standard visual spatial training treatment provided in the OT department).
Patients will undergo thorough evaluation of neglect and will undergo PET procedure before being transferred to rehabilitation. Patient will receive intensive rehabilitation for 15 sessions of the cognitive treatment and 15 session of motor training. After this period patient will undergo another PET procedure to assess any changes in brain activation. Patient will then return to rehabilitation as needed.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||6 participants|
|Intervention Model:||Parallel Assignment|
|Official Title:||Effectiveness of Rehabilitation (Phasic Alerting and Visual Spatial Scanning Training) on the Recovery of Patients Post Right Stroke With Unilateral Spatial Neglect: Using Functional Imaging PET and Standardized Neurobehavioral and Functional Tests|
- This study's aim is to examine the functional reorganization of the attentional network in the brain of USN patients while performing visual tasks, by means of functional neuroimaging techniques, in light of specific rehabilitation techniques.
- The aim of this study is to try and contribute to both efforts by examining treatment effectiveness of two methods; one targeting general arousal (phasic alerting), and the other targeting increasing awareness to left side stimuli and habit changes.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00305513
|Contact: Zeev Meiner, MD||00 972 2 5844582||MEINER@hadassah.org.il|
|Hadassah Medical Organization||Not yet recruiting|
|Jerusalem, Israel, 91120|
|Contact: Arik Tzukert, DMD 00 972 2 6776095 firstname.lastname@example.org|
|Principal Investigator: Zeev Meiner, MD|
|Principal Investigator: Roland Chishin, MD|
|Principal Investigator:||Zeev Meiner, MD||Hadassah Medical Organization|