To Investigate the Event Related Potentials (ERPs) of Patients With Brain Lesions
Recruitment status was Recruiting
| Tracking Information | |
|---|---|
| First Received Date ICMJE | December 3, 2010 |
| Last Updated Date | December 3, 2010 |
| Start Date ICMJE | September 2010 |
| Estimated Primary Completion Date | September 2011 (final data collection date for primary outcome measure) |
| Current Primary Outcome Measures ICMJE | Not Provided |
| Original Primary Outcome Measures ICMJE | Not Provided |
| Change History | No Changes Posted |
| Current Secondary Outcome Measures ICMJE | Not Provided |
| Original Secondary Outcome Measures ICMJE | Not Provided |
| Current Other Outcome Measures ICMJE | Not Provided |
| Original Other Outcome Measures ICMJE | Not Provided |
| Descriptive Information | |
| Brief Title ICMJE | To Investigate the Event Related Potentials (ERPs) of Patients With Brain Lesions |
| Official Title ICMJE | Not Provided |
| Brief Summary | Event-related potentials (ERPs)has the advantage of excellent temporal resolution on measuring real-time neural activities that reflect to higher level cognitive processes. A research project related to lesion studies in which patients with cognitive function impairment and communication disorder will be recruited as participants to examine their impairment as well as residual abilities by using ERPs. Hopefully, expected findings will provide further analysis based on the patterns of neural activities revealed by both patients and normal controls should be able to provide important evidence toward building the cross-linguistic theory. The findings also have applications on diagnostic and evaluation for patients with brain lesions for clinical application with communication disorder. |
| Detailed Description | Not Provided |
| Study Type ICMJE | Observational |
| Study Design ICMJE | Observational Model: Case Control Time Perspective: Prospective |
| Target Follow-Up Duration | Not Provided |
| Biospecimen | Not Provided |
| Sampling Method | Non-Probability Sample |
| Study Population | patients with brain lesions young normal controls old normal controls |
| Condition ICMJE | Brain Lesions |
| Intervention ICMJE | Not Provided |
| Study Group/Cohort (s) |
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| Publications * | Not Provided |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |
| Recruitment Status ICMJE | Recruiting |
| Estimated Enrollment ICMJE | 90 |
| Completion Date | Not Provided |
| Estimated Primary Completion Date | September 2011 (final data collection date for primary outcome measure) |
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both |
| Ages | Not Provided |
| Accepts Healthy Volunteers | Yes |
| Contacts ICMJE | Not Provided |
| Location Countries ICMJE | Taiwan |
| Administrative Information | |
| NCT Number ICMJE | NCT01254500 |
| Other Study ID Numbers ICMJE | DMR-100-108 |
| Has Data Monitoring Committee | Not Provided |
| Responsible Party | Sui Foon Lo, China Medical University Hospital |
| Study Sponsor ICMJE | China Medical University Hospital |
| Collaborators ICMJE | Not Provided |
| Investigators ICMJE | Not Provided |
| Information Provided By | China Medical University Hospital |
| Verification Date | December 2010 |
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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