Stroke Clinical Trial
— TelexOfficial title:
Home Based Tele-exercise for People With Chronic Neurological Impairments
Verified date | January 2023 |
Source | Burke Medical Research Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
To assess the impact of a 12-week virtual seated physical intervention on cardiovascular health and wellness in people with chronic neurological impairments (CNI).
Status | Active, not recruiting |
Enrollment | 60 |
Est. completion date | December 31, 2024 |
Est. primary completion date | December 31, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: 1. Participants with chronic (>6 months) neurological impairments 2. 18 to 75 years of age 3. Participants who can provide a medical clearance to participate in the program 4. Participants who can remain seated for at least one hour 5. Heart rate/BP considerations, per each participant's MD 6. Participants must be able to don/doff HR monitor without assistance, or have assistance if necessary 7. Participants must maintain their current exercise/physical activity routine during the course of the study 8. Clinically stable with no other neurological, medical or cognitive impairments 9. Reliable Internet connection and ability to use Zoom platform 10. Participants must speak and understand English 11. No contraindication/limitations to exercise 12. Currently exercising 2 days or less per week Exclusion Criteria: 1. Participants with any cognitive impairment preventing safe and accurate participation in the program 2. Medical issues preventing safe participation 3. Other problems possibly contraindicating autonomous exercise at home if no supervision available. |
Country | Name | City | State |
---|---|---|---|
United States | Burke Neurological Institute | White Plains | New York |
Lead Sponsor | Collaborator |
---|---|
Burke Medical Research Institute |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in heart rate | Heart rate on last day of training compared to heart rate on first day of training | Within one week before the first intervention session to within one week after the end of intervention | |
Secondary | Perceived Wellness Survey | a 36-item instrument used to measure an individual's perceived health status in physical, psychological, emotional, intellectual, spiritual, and social wellness constructs | Within one week before the first intervention session to within one week after the end of intervention | |
Secondary | Physical Activity Enjoyment Scale | a self-assessment measure of enjoyment with their current physical activity | Within one week before the first intervention session to within one week after the end of intervention | |
Secondary | Short Form-36 Health Survey | measures physical health and mental health | Within one week before the first intervention session to within one week after the end of intervention | |
Secondary | Numerical pain rating | standardized instrument for pain assessment in clinical and research practice. It is an 11-point scale from 0 (no pain) to 10 (the most intense pain) at rest and during movement | Within one week before the first intervention session to within one week after the end of intervention | |
Secondary | Borg's Rating Scale of Perceived Exertion | standardized measure to evaluate perceived intensity of exertion, effort, and fatigue during physical exercise | Within one week before the first intervention session to within one week after the end of intervention | |
Secondary | Reason for exercise inventory | is a 24-item scale to assess the reason that motivates a person to exercise | Within one week before the first intervention session to within one week after the end of intervention |
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