Executive Dysfunction Clinical Trial
— NIBSOfficial title:
Improving Mobility and Cognition in Older Adults: Establishment of an Interdisciplinary Clinical Research Program Using Non-Invasive Brain Stimulation
NCT number | NCT02740530 |
Other study ID # | 107526 |
Secondary ID | |
Status | Terminated |
Phase | N/A |
First received | |
Last updated | |
Start date | April 2016 |
Est. completion date | May 2023 |
Verified date | March 2024 |
Source | Lawson Health Research Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study aims to test the efficacy of a type of non-invasive brain stimulation (NIBS), known as repetitive transcranial magnetic (rTMS) stimulation, in improving mobility, particularly gait stability and variability, and executive dysfunction in older adults. The study will be conducted in forty older adults (≥60 years) with a diagnosis of executive dysfunction.
Status | Terminated |
Enrollment | 25 |
Est. completion date | May 2023 |
Est. primary completion date | March 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 60 Years and older |
Eligibility | Inclusion Criteria: - Having executive dysfunction (defined as score below 11 out of a possible 13 in the "Montreal Cognitive Assessment -MoCA- executive score index") - Age 60 years and older - English speaking - Able to ambulate 10m independently without any gait aid (eg. walker, cane) Exclusion Criteria: - Unable to understand or communicate in English - Parkinsonism or any neurological disorder with residual motor deficit (eg. Major stroke, epilepsy) - Musculoskeletal disorder detected by clinical examination which affects gait performance -Active osteoarthritis affecting lower limbs (American College of Rheumatology criteria) - Severe depression operationalized as Geriatric Depression Scale (GDS) score>10 TMS specific exclusion criteria: - Persons with metal anywhere in the head, excluding the mouth, including shrapnel, and screws and clips from surgical procedures - Persons with cardiac pacemakers, implanted medication pumps, electrodes inside the heart - Unstable heart disease - Persons with increased intracranial pressure, as in acute large infarctions or trauma - Previous major stroke, history seizure, Parkinson D, Huntington D. - History of schizophrenia/schizo-affective disorder, substance use disorder within 1 year of study |
Country | Name | City | State |
---|---|---|---|
Canada | Parkwood Institute | London | Ontario |
Lead Sponsor | Collaborator |
---|---|
Lawson Health Research Institute |
Canada,
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* Note: There are 23 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Gait variability which is calculated as coefficient of variation (CoV) | Seven days | ||
Primary | Gait velocity - cm/s | Seven days | ||
Secondary | Executive function, assessed as time to take to complete Trail Making A and B (TMT A and B) in seconds. | seven days |
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