Not yet recruiting NCT06998017
The Feasibility of LVHIIT on Inpatient Stroke Rehab
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Low Volume High Intensity Interval Training.
- Who it may be relevant to
- Registry conditions: Stroke, High Intensity Interval Training, Aerobic Fitness, Physical Therapy. Basic parameters: 18 years — 85 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
The Feasibility of Low-Volume High Intensity Interval Training on Inpatient Stroke Rehab
Overview
The objective of this study is to explore the safety and feasibility of conducting low-volume, high-intensity interval training (HIIT) on a total body recumbent stepper (TBRS) in persons with stroke in an inpatient rehabilitation setting.
Interventions
- Other Low Volume High Intensity Interval Training
Participants will conduct aerobic exercise on a total body recumbent stepper to get their heart rates to levels consistent with high intensity exercise.
Primary outcome measures
- Safety of LVHIIT (low volume high intensity interval training) on total body recumbent stepper [Time frame: 2-3 months]
- Adherence of LVHIIT (low volume high intensity interval training) on total body recumbent stepper [Time frame: 2-3 months]
- Attainment of LVHIIT (low volume high intensity interval training) on total body recumbent stepper [Time frame: 2-3 months]
- Acceptability of LVHIIT (low volume high intensity interval training) on total body recumbent stepper [Time frame: 2-3 months]
Eligibility criteria
Inclusion criteria
- -Both sexes between the age of 18-85 years at time of consent
- Ischemic or hemorrhagic stroke at consent. People with stroke and newly diagnosed cardiovascular complications had >50% prevalence of recurrent stroke at 5 years. Index stroke or recurrent stroke on same side as index stroke will be allowed.
- Exercise continuously for minimum of 30 watts for 3 minutes on the recumbent stepper to demonstrate ability to perform the exercise test or therapist confirmation/documentation of participant's ability to use the recumbent stepper.
- No aerobic exercise contraindications or other safety/physical concerns during the submaximal exercise test determined by the therapy team or inpatient physicians.
- Able to communicate with investigators, follow 2-step command \& correctly answer consent comprehension questions
Exclusion criteria
- Implanted pacemaker or defibrillator limiting exercise performance
- Reported pain that limits or interferes with activities of daily living and physical activity/exercise
- Acute Myocardial Infarction in the last 2 days
- Ongoing unstable Angina
- Active Endocarditis
- Symptomatic Severe Aortic Stenosis
- Decompensated Heart Failure
- Acute Pulmonary Embolism, Pulmonary Insufficiency, or Deep Veinous Thrombosis
- Acute Myocarditis or Pericarditis
- Other significant neurologic, orthopedic, or peripheral vascular conditions that would limit exercise participation
- Oxygen-dependent chronic obstructive pulmonary disease
- Neurological disease (Multiple Sclerosis, Alzheimer's disease, Parkinson's disease)
- Pregnancy
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Other
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06998017 · STUDY00160192