← Back to Search

Seated Exercise for Neurological Disorders (Telex Trial)

N/A
Waitlist Available
Led By Kathleen Friel
Research Sponsored by Burke Medical Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Clinically stable with no other neurological, medical or cognitive impairments
Participants with chronic (>6 months) neurological impairments
Must not have
Participants with any cognitive impairment preventing safe and accurate participation in the program
Timeline
Screening 3 weeks
Treatment Varies
Follow Up within one week before the first intervention session to within one week after the end of intervention
Awards & highlights
No Placebo-Only Group

Summary

This trial looks at whether a 12-week virtual seated physical intervention can improve cardiovascular health and wellness in people with chronic neurological impairments.

Who is the study for?
This trial is for adults aged 18-75 with chronic neurological impairments like stroke, multiple sclerosis, or cerebral palsy. They must be stable medically and cognitively, able to use Zoom and a heart rate monitor independently (or have help), speak English, and not exercise more than twice a week. Medical clearance is required.
What is being tested?
The study tests the effects of a 12-week home-based seated exercise program delivered virtually on cardiovascular health in people with long-term (>6 months) neurological conditions. Participants will maintain their usual physical activity levels during the trial.
What are the potential side effects?
Since this intervention involves seated exercises tailored to individuals with chronic neurological impairments, side effects might include muscle soreness or fatigue. However, any serious risks are minimized by requiring medical clearance before participation.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am mentally and physically stable with no serious health issues.
Select...
I have had a neurological condition for more than 6 months.
Select...
I can put on and take off a heart rate monitor by myself or with help.
Select...
I am between 18 and 75 years old.
Select...
I am between 18 and 75 years old.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I do not have any cognitive impairments that prevent me from safely participating.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~within one week before the first intervention session to within one week after the end of intervention
This trial's timeline: 3 weeks for screening, Varies for treatment, and within one week before the first intervention session to within one week after the end of intervention for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in heart rate
Secondary study objectives
Borg's Rating Scale of Perceived Exertion
Numerical pain rating
Perceived Wellness Survey
+3 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Live zoom exercise classesExperimental Treatment1 Intervention
Participants will engage in a live zoom exercise session. Participants will undergo 45 minutes of aerobic exercise intervention, three times a week, for a period of 12 weeks. Exercise will include repetitive bouts of high intensity exercises with intermittent periods of rest or active recovery. circuit of moves like 'jabs', 'hooks' etc, and a strength and endurance class that promotes postural awareness.
Group II: Recorded zoom exercise classesActive Control1 Intervention
Participants will undergo 45 minutes of aerobic exercise intervention, three times a week, for a period of 12 weeks, using a pre-recorded class that they can do according to their own schedule. Exercise will include repetitive bouts of high intensity exercises with intermittent periods of rest or active recovery. circuit of moves like 'jabs', 'hooks' etc, and a strength and endurance class that promotes postural awareness.

Find a Location

Who is running the clinical trial?

Burke Medical Research InstituteLead Sponsor
23 Previous Clinical Trials
1,405 Total Patients Enrolled
Kathleen FrielPrincipal InvestigatorBurke Medical Research Institute

Media Library

Seated exercise Clinical Trial Eligibility Overview. Trial Name: NCT04564495 — N/A
Overactive Bladder Research Study Groups: Live zoom exercise classes, Recorded zoom exercise classes
Overactive Bladder Clinical Trial 2023: Seated exercise Highlights & Side Effects. Trial Name: NCT04564495 — N/A
Seated exercise 2023 Treatment Timeline for Medical Study. Trial Name: NCT04564495 — N/A
~13 spots leftby Nov 2025