Parkinson's Disease Clinical Trial
Official title:
The Effect of Speed of Processing Training on Pedestrian Behavior in Patients With Parkinson's Disease and Healthy Older Adults
Verified date | March 2018 |
Source | University of Alabama at Birmingham |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this prospective, within-subject randomized cross-over design study is to determine if a computer training program (Speed of Processing Training - SOPT) improves safe pedestrian behavior in patients with Parkinson's disease and in healthy older adults in a virtual reality pedestrian environment. Pedestrian injury poses significant risk to healthy older adults and patients with Parkinson's disease. Several age-related changes, including slowing of visual processing speed, increase risky pedestrian behavior. This study will determine if SOPT improves pedestrian behavior in patients with Parkinson's disease and healthy older adults and evaluate the persistence of the SOPT training effects.
Status | Completed |
Enrollment | 88 |
Est. completion date | February 2018 |
Est. primary completion date | February 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 50 Years and older |
Eligibility |
Inclusion Criteria Parkinson's disease Subjects: - Subjects with a clinical diagnosis of idiopathic Parkinson's disease based on the presence of bradykinesia and one or both of the following: rest tremor and/or rigidity - On stable medications for at least 4 weeks prior to entering the study and expected to not need any medication changes for the duration of the study - Age =50 at the time of entry into the study - Age of onset of Parkinson's disease 45 - 85 years old - Asymmetric onset of PD - Progressive motor symptoms of PD - Hoehn and Yahr stages 1-4 - Ability to walk up and down a single stair step - Access to a computer with internet Exclusion Criteria Parkinson's disease Subjects: - Atypical features indicative of a Parkinson's Plus disorder (Progressive Supranuclear Palsy, Multiple Systems Atrophy, Corticobasal Degeneration) including cerebellar signs, supranuclear gaze palsy, apraxia, prominent autonomic failure, or other cortical signs. - Neuroleptic treatment at time of onset of Parkinsonism - Active treatment with a neuroleptic at time of study entry - History of multiple strokes with stepwise progression of Parkinsonism - History of multiple head injuries - Inability to walk without assistance, including a cane, wheelchair, or walker - Cognitive dysfunction that would prevent subject's ability to perform virtual reality simulation, speed of processing training, or complete questionnaire - Blindness - Any medical condition that, based on discretion of the PI, would prevent the subject's ability to participate in the study Inclusion Criteria Control Subjects: - Age =50 at the time of entry into the study - On stable medications for at least 4 weeks prior to entering the study and expected to not need any medication changes for the duration of the study - Ability to walk up and down a single stair step - Access to a computer with internet Exclusion criteria Control Subjects: - Parkinson's disease or other neurodegenerative disorder - Inability to walk without assistance, including a cane, wheelchair, or walker - Cognitive dysfunction that would prevent subject's ability to perform virtual reality simulation, speed of processing training, or complete questionnaires - Blindness - Any medical condition that, based on the discretion of the PI, would prevent the subject's ability to participate in the study |
Country | Name | City | State |
---|---|---|---|
United States | University of Alabama at Birmingham | Birmingham | Alabama |
Lead Sponsor | Collaborator |
---|---|
University of Alabama at Birmingham | National Institute on Aging (NIA) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Time to contact | Difference in time to contact between baseline and immediate post-training assessments in PD and healthy controls | 3 months | |
Secondary | Useful Field of View (UFOV) | Difference in UFOV total score between baseline and immediate post-training assessments in PD and healthy controls | 3 months | |
Secondary | Executive function (MoCA, Trails, Stroop) | Difference in MoCA, Trails, and Stroop between baseline and immediate post-training assessments in PD and healthy controls | 3 months | |
Secondary | Vigilance | Differences in vigilance as measured by psychomotor vigilance task between baseline and immediate post-training assessments in PD and healthy controls | 3 months |
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