NCT03399929 · Centre for Neuro Skills
Traumatic Brain Injury and Stroke Long Term Outcome
What this study is about
Investigators will determine the long-lasting effects of post-acute rehabilitation after traumatic brain injury and stroke. Investigators will also evaluate if the beneficial effects of rehabilitation continue after discharge from a rehabilitative program.
View original scientific description
Investigators will determine the long-lasting effects of post-acute rehabilitation after traumatic brain injury and stroke. Investigators will also evaluate if the beneficial effects of rehabilitation continue after discharge from a rehabilitative program.
Interventions
OTHER
Post Acute Rehabiltation
Primary outcome measures
Effects of rehabilitation on long term occupational Status after injury
Time frame: 1 to 10 years
Occupational Status Questionnaire
Effects of rehabilitation on long term cognitive function after injury
Time frame: 1 to 10 years
Brief Test of Adult Cognition by Telephone
Effects of rehabilitation on long term disability function after injury
Time frame: 1 to 10 years
Supervision Rating Scale and Disability Rating Scale
Effects of rehabilitation on long term quality of life after injury
Time frame: 1 to 10 years
Quality of Life in Neurological Disorders Measures (NeuroQOL)
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- Endured a traumatic brain injury or stroke
- Subject or caretaker should be Fluent in English
Exclusion criteria
- Diagnosis of degenerative neurological disease prior to sustaining stroke or traumatic brain injury
- b) A history of major psychosis as defined by Diagnostic and Statistical Manual of Mental Disorders (DSM-V) prior to sustaining stroke or traumatic brain injury
Where
- Encino, California
Related conditions & keywords
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Jul 20, 2022 · Source of record for eligibility and locations