Skip to content

Effects of Heating on Exercise Pressor Reflex in Peripheral Artery Disease: Exercise Ability

Effects of Heating on Exercise Pressor Reflex in Peripheral Artery Disease: Exercise Ability

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03900832
Acronym
EPR
Enrollment
33
Registered
2019-04-03
Start date
2019-05-15
Completion date
2025-07-31
Last updated
2025-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

PAD

Keywords

exercise, blood pressure response, heating

Brief summary

The study objectives of this projects are to examine the hypothesis that the sympathetic and blood pressure responses to exercise will be attenuated during and after heat exposure in patients with peripheral artery disease, via altering the sensitivity of the muscle afferent receptors.

Detailed description

Peripheral arterial disease (PAD) affects 8-12 million Americans and its cardinal symptom is leg pain during exercise, termed intermittent claudication. The diagnosis of PAD involves measuring the ankle-brachial index (ABI, i.e. the systolic pressure in the ankle divided by the systolic pressure in the arm); values below 0.9 are indicative of large vessel obstruction. Intermittent claudication is the most common symptom of this disease and it regularly occurs during exercise/physical activity but is relieved promptly by rest. Previous studies suggest that as the exercise pressor reflex is activated in patients with PAD, BP and heart rate (HR) are exaggerated. The BP rises during walking in the PAD patients were significantly greater than that seen in healthy control subjects. A recent human study from our group further indicates that an early BP response occurred during plantar flexion exercise before claudication was noted by the subjects, which may suggest that the accentuated BP response was due to an augmented muscle mechanoreflex in PAD. Moreover, another recent study from our group also showed that PAD patients have augmented renal vasoconstriction during plantar flexion exercise. It has been shown that exercise has benefits for patients with PAD. However, exercise becomes limited due to the pain and fatigue associated with the disease. Moreover, the augmented pressor response to exercise in PAD may increase the risk for the end organ damage (e.g. brain and/or heart). Thus, finding alternate/complimentary interventions that modulate the cardiovascular system and autonomic nervous system, and can be tolerated by the patients, would be beneficial. One possible intervention is heat exposure, since acute bouts of exercise and acute heat exposure have similar acute effects on both the autonomic and cardiovascular systems. For example, both exercise and heat exposure increase body temperature, increase HR, increase cardiac output (CO), increase left ventricular ejection fraction (EF), and enhance myocardial function. In the peripheral circulation, both exercise and heat exposure increase limb blood flow , muscle blood flow, and skin blood flow. Moreover, recent studies suggest that whole body exposure improves the endothelium function in PAD patients (e.g. activates endothelial progenitor cells CD34+). However, the effect of heat treatment on the ability of walking of PAD patients has not been examined. Moreover, it is unknown if heating can normalize/decrease the accentuated the pressor responses to exercise in PAD patients.

Interventions

OTHERWithout Heating

Subject will complete walking protocol without any heating procedure

OTHERWarm Bath

Subjects will sit in a warm bathtub with water up to their shoulders, while one arm will be out of water for BP and HR measurement. The water temperature and internal temperature (Tcore), BP and HR will be measured throughout the bath. The water temperature will be controlled between 38-41°C. Subjects will remain in the tub for ≤ 30 minutes. If the HR increases more than 15 -20 bpm, or a significant BP drop occurs (e.g. BP \>20 mmHg), the subject will be removed from the bath even if the time is \<30 min.

OTHERNeutral Bath

Subjects will sit in a warm bathtub with water up to their shoulders, while one arm will be out of water for BP and HR measurement. The water temperature and internal temperature (Tcore), BP and HR will be measured throughout the bath. The water temperature will be controlled between 35 - 37°C. Subjects will remain in the tub for ≤ 30 minutes.

OTHERHeating Suit

The mean skin temperature Tsk will be controlled with a water-perfused suit worn by subjects. Whole-body heating will be accomplished by perfusing warm water (\ 45 - 50 °C) through the suit to elevate the Tsk to ≤ 38 °C (100 oF). Warm water is through plastic tubes, and subjects' skin will not directly touch warm water. The heating will be continued until the ∆Tcore reaches \ 0. 6 - 1.0 °C. This may take approximately 60 - 90 min.

OTHERLower limb warm water immersion

Subjects will sit on a chair and put their lower legs and feet in a bucket with warm water. The water level will be just below the knees (depth of approximately 40 cm). The water temperature will be monitored and controlled at \ 38 - 42 °C throughout the 30 minutes. BP, HR, Tcore, the skin temperature and skin blood flow (e.g. on a thigh and/or forearm) will be measured before, during and after the lower limbs warm water immersion.

OTHERGardner walking protocol

The Gardner protocol begins at 2 mph and 0% grade for 2 minutes. The grade increases by 2% every 2 minutes (the speed remains 2 mph) until the subject says they want to stop or 22 minutes maximum. BP and HR will also be measured throughout the protocol.

Sponsors

Milton S. Hershey Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)

Masking description

Subjects will be aware if they are being heated or not, but data analysis process is blinded.

Intervention model description

The investigators will examine (using a prospective observational design) if heating will affect walking ability, blood pressure and heart rate responses in PAD patients. Each subject will serve as their own control. Additionally, we will compare these responses between PAD patients and healthy controls subjects.

Eligibility

Sex/Gender
ALL
Age
21 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

All subjects * Capable of giving informed consent * Any race or ethnicity * Men and women age 21- 85 years (inclusive) * Fluent in written and spoken English Patients with peripheral arterial disease (PAD) * Diagnosed with PAD (i.e., ankle-brachial index below 0.9) * Fontaine stage II or less - no pain while resting * Satisfactory history and physical exam Healthy subjects * Satisfactory history and physical examination * Free of acute medical conditions

Exclusion criteria

For patients with PAD and Healthy subjects * Age \< 21 years * Pregnant or nursing women * Decisional impairment * Prisoners For patients with PAD * History of CAD with symptoms of unstable angina or myocardial infarction (\<6 months) * History of epilepsy or seizure disorders For healthy subjects • Any other chronic diseases (heart, lung, neuromuscular disease or diabetes)

Design outcomes

Primary

MeasureTime frameDescription
Walking time in minutesRecording walking time to fatigue (up to 22 minutes maximum) during of every 3-4 hour study visit.Walking time on treadmill using Gardner protocol
Blood pressure in mmHgRecorded continuously during the 3-4 hour study visitCuffs placed on a finger and arm will monitor blood pressure.
Heart Rate in beats per minuteRecorded continuously during the 3-4 hour study visitElectrocardiogram (ECG) patches attached to a Cardiocap will monitor heart rat

Secondary

MeasureTime frameDescription
Internal Temperature in degrees CRecorded continuously during the 3-4 hour study visitThe internal temperature (Tcore) will be measured from the stomach/intestines via a telemetry pill swallowed by subjects.
Near infrared spectroscopy (NIRS) in arbitrary unitsRecorded continuously during the 3-4 hour study visitThis system is designed specifically for non-invasive measurements of muscle tissue. The system measures the tissue saturation of the investigated muscle, called the 'tissue saturation index' (TSI).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026