RECRUITINGINTERVENTIONAL

Passive Limb Movement Study

About This Trial

Stroke survivors have compromised vascular function which may contribute to secondary stroke risk, cardiovascular disease, and may limit their exercise tolerance. No studies have examined how femoral blood flow responds to both passive leg movement, a measure of microvascular function, as well as active leg contractions, a measure of the hyperemic response to exercise. Leg muscles with a reduced blood flow response to movement could be associated with decreased neuromuscular function, such as leg strength and fatigue. Preliminary data showing a single bout of ischemic conditioning may improve vascular function and muscle activation in healthy adults and individuals post-stroke. Therefore, the investigators want to examine if ischemic conditioning will also improve the blood flow response to passive leg movements as well as during single leg active contractions.

Who May Be Eligible (Plain English)

Who May Qualify: - Individuals Post-Stroke - 18 - 85 years of age - Cortical or sub-cortical stroke ≥ 6 months ago with residual hemiparesis - Able to give willing to sign a consent form and follow 2-step command. - English Speaking - Age- and Sex-Matched Controls (CON) - Matched to age of individual post- stroke ± 5 years. - Matched to sex of individual post-stroke - Able to give willing to sign a consent form and follow 2-step command. - English Speaking - Young Healthy Adults (CONyoung) - Age 18-30 years old - Able to give willing to sign a consent form and follow 2-step command. - English Speaking Who Should NOT Join This Trial: - All Groups - Unable to stand from chair and walk 10 meters without physical assistance from another person (able to use assistive device). - History of blood clots in the extremities or any condition in which compression of the thigh or transient ischemia is contraindicated (i.e., wounds in the leg). - Chronic lasting symptoms (\> 6 months) of severe COVID-19 (i.e., hospitalization) - Low back or hip pain that limits lower extremity motor testing. - History of head trauma or concussion within the past 6 months - Comorbid neurological disorder - Peripheral vascular disease - Myocardial infarction in the previous year - Condition where fatiguing contractions or resisted leg contractions are contraindicated - Resting SBP ≥180 mmHg or DBP ≥ 100 mmHg - Pregnancy or breastfeeding. - Other significant medical condition likely to influence study or jeopardize safety as assessed by the Primary Investigator - CON and CONyoung - History of Stroke Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language

Inclusion Criteria: * Individuals Post-Stroke * 18 - 85 years of age * Cortical or sub-cortical stroke ≥ 6 months ago with residual hemiparesis * Able to give informed consent and follow 2-step command. * English Speaking * Age- and Sex-Matched Controls (CON) * Matched to age of individual post- stroke ± 5 years. * Matched to sex of individual post-stroke * Able to give informed consent and follow 2-step command. * English Speaking * Young Healthy Adults (CONyoung) * Age 18-30 years old * Able to give informed consent and follow 2-step command. * English Speaking Exclusion Criteria: * All Groups * Unable to stand from chair and walk 10 meters without physical assistance from another person (able to use assistive device). * History of blood clots in the extremities or any condition in which compression of the thigh or transient ischemia is contraindicated (i.e., wounds in the leg). * Chronic lasting symptoms (\> 6 months) of severe COVID-19 (i.e., hospitalization) * Low back or hip pain that limits lower extremity motor testing. * History of head trauma or concussion within the past 6 months * Comorbid neurological disorder * Peripheral vascular disease * Myocardial infarction in the previous year * Condition where fatiguing contractions or resisted leg contractions are contraindicated * Resting SBP ≥180 mmHg or DBP ≥ 100 mmHg * Pregnancy or breastfeeding. * Other significant medical condition likely to influence study or jeopardize safety as assessed by the Primary Investigator * CON and CONyoung * History of Stroke

Treatments Being Tested

DEVICE

Ischemic Conditioning

The cuff will be placed around the proximal, paretic thigh (or dominant thigh for controls) and inflated for 5 minutes in a supine or semi-reclined position, then released for a 5-minute recovery period. Five cycles of inflation and recovery will be performed (45 minutes total).These inflations will be done using a cuff similar to what is used for taking blood pressure.

Locations (1)

Medical College of Wisconsin

Milwaukee, Wisconsin, United States