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Peripheral Arterial DiseasePhase 1NCT05335161

A New Heat Therapy Device for Home-based Leg Heating in Patients With Lower-extremity Peripheral Artery Disease

A Phase 1 study testing Home-based leg heat therapy in people with Peripheral Arterial Disease and Intermittent Claudication, run by Purdue University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of the proposed pilot study is to evaluate the feasibility of a new leg heat therapy system treatment for patients with lower extremity PAD. The new system is comprised of leg-length water circulating pads surrounded by a separate pneumatic compression outer garment that compresses the pads against the skin… Read more about this study

Who is it for?
Ages 60 years and older
What is being tested?
Home-based leg heat therapy
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
6 participants
Where
1 siteUnited States
Study dates
30 May 2023to 7 Feb 2024
Phase
Phase 1
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 60 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Men and women 60 years or older
  • Resting ankle-brachial index (ABI) of 0.9 or less in at least one leg.
  • Individuals with a resting ABI between 0.91 and 1.00 at baseline will be eligible if their ABI drops by 20% or greater following a heel-rise test.

Who cannot join

  • Critical limb ischemia (ischemic rest pain or ischemia-related, non-healing wounds or tissue loss)
  • Prior amputation
  • Exercise tolerance limited by factors other than leg pain (e.g. angina, arthritis, severe lung disease, etc).
  • Recent (<3 months) lower-extremity revascularization or orthopedic surgery
  • Use of walking aid other than a cane
  • Active cancer
Show all 11Show fewer
  • Chronic kidney disease (eGFR <30 by MDRD or Mayo or Cockcroft-Gault formula)
  • Unable to fit into water-circulating trousers
  • A Mini-Mental Status Examination score <23
  • Impaired thermal sensation in the leg
  • Age lower than 60 yrs

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Purdue University

    West Lafayette, Indiana, 47907

Other trials in United States

About this study

Official title: A New Heat Therapy Device for Home-based Leg Heating in Patients With Lower-extremity Peripheral Artery Disease: a Pilot Study

The goal of the proposed pilot study is to evaluate the feasibility of a new leg heat therapy system treatment for patients with lower extremity PAD. The new system is comprised of leg-length water circulating pads surrounded by a separate pneumatic compression outer garment that compresses the pads against the skin for efficient heat transfer. The new leg garment is easily closed with a zipper. The air chambers automatically adjust the amount of air inflation enabling use of the garment independent of patient leg size. Six patients with PAD will be asked to complete daily (90 min/day) home-based leg HT for 12 weeks using the newly developed system. The primary study outcome is the change from baseline in walking performance on the 6-minute walk test at the 12-week follow-up. Secondary outcomes include plantar flexion power, as assessed using isokinetic dynamometry, sit-to-stand muscle power and perceived quality of life.

Read the detailed description

Lower-extremity PAD is a manifestation of systemic atherosclerosis associated with increased risk of cardiovascular morbidity and mortality, diminished quality of life, physical functioning and psychological well-being. In 2015, an estimated 236 million people worldwide, most between 65 and 69 years of age, were living with PAD. Home-based leg heat therapy (HT) is emerging as a potential effective and practical treatment to increase leg blood flow and improve walking performance in patients with symptomatic PAD. In the first randomized sham-controlled trial to examine the benefits of supervised leg HT in patients with symptomatic PAD (90 min, 3 days/week for 6 weeks), we demonstrated that patients assigned to the leg heating group displayed a clinically meaningful improvement in perceived physical functioning. Building upon these findings, we recently completed a NIH-sponsored randomized clinical trial to examine the safety, tolerability, and effectiveness of home-based, unsupervised leg HT (90 min, 7 days/week for 8 weeks) in 34 patients with symptomatic PAD. Patients randomized to the HT group displayed an increase in 6-minute walk from baseline of 23 meters after 8 weeks of treatment, which is clinically meaningful for PAD patients. Importantly, home-based leg HT was also found to be safe (no skin injury), well-tolerated, and patient compliance was surprisingly high (96% completion of the prescribed treatment sessions).

Heat packs, electric heating pads, and electric blankets are widely available, but have high risk of contact burns, particularly in patients with peripheral neuropathy that is commonly associated with diabetes mellitus and PAD. An assembly of individual pads is difficult to apply and skin contact is unreliable. Water-circulating pads have been found to be safer than electric devices because they provide more reliable thermostatic control. PAD patients with diffuse bilateral disease often accompanied by neuropathy need a reliable system that is simple to operate, easy to put on, covers the entirety of both lower limbs and safely provides HT while avoiding skin injury. Currently, there is no commercially-available HT system for home-based therapy in elderly individuals, despite the documented benefits associated with repeated HT. To address this unmet clinical need, Aquilo Sports is developing a system that will monitor skin temperature and have an integrated shut-off feature to prevent skin burns, and record treatment sessions to confirm patient compliance. The system has undergone extensive independent validation testing and has been widely adopted by professional athletes. The garment is easily closed with a zipper and auto-adjusts pneumatically to different leg sizes.

Our objective is to establish evidence to support the safety and feasibility of the redeveloped Aquilo system during repeated home-based treatment in patients with PAD. Our approach to testing our hypothesis will be to ask 6 patients with PAD to undergo daily home-based leg HT (90 min/day, 7 days/week) for 12 weeks. The length of the intervention (12 weeks) was selected as it is similar to: 1) the duration of previous studies with other HT modalities showing beneficial effects in patients with PAD, 2) the recommended minimal duration of exercise training interventions, the gold standard treatment for PAD.

The primary study outcome is the change from baseline in walking performance on the 6-minute walk test at the 12-week follow-up. Secondary outcomes include plantar flexion power, as assessed using isokinetic dynamometry, sit-to-stand muscle power and perceived quality of life.The study coordinator will call patients weekly to record the occurrence of adverse events.

Being tested
Home-based leg heat therapy
Keywords
heat therapy, peripheral artery disease
Medical subject headings
Peripheral Arterial Disease, Intermittent Claudication, Hyperthermia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Home-based leg heat therapyDevice

    Also called Aquilo Sports

    The Aquilo system consists of a garment that contains an inner water-circulating pad that is compressed by air bladders. The volume of air inflating the air bladders is pressure-controlled so the garment automatically adjusts to the shape and size of all legs. The touch screen console contains pre-programmed settings for ease of use. After baseline characteristics are established, patients will be provided with the Aquilo device and will be instructed on how to operate the equipment and how to rapidly remove the system if the alarm sounds or if they have any unusual feeling. Patients in both groups will also receive a logbook to record their sessions. Patients will undergo daily home-based leg HT (90 min/day, 7 days/week) for 12 weeks. Water at 42ºC will be perfused through the water-circulating garment for 90 min, with the goal of increasing skin temperature in the calf to ~37ºC.

Study groups in NCT05335161
Study groupRoleWhat they receive
Home-based leg heat therapyExperimentalPatients will be provided with the Aquilo heat therapy device and will be instructed on how to operate the equipment. The device will be used in accordance to the manufacturers recommendations. Patients will be asked to apply the therapy daily in the home setting for 12 week (90 min/day, 7 days/week).
Receives: Device: Home-based leg heat therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Six-minute Walk Distance

    Participants will receive standardized instructions and will be asked to walk the greatest distance possible by walking back and forth along a 100-ft corridor for 6 min.

    Measured: Baseline to 12-week follow-up

Secondary outcomes (4)
  1. Change in Walking Impairment Questionnaire Score

    This disease-specific questionnaire assess the ability of patients with PAD to walk defined distances and speeds and to climb stairs, with scores ranging from 0 to 100. Higher scores indicate better walking ability (i.e., better outcome). Lower scores indicate greater walking impairment (i.e., worse outcome)

    Measured: Baseline to 12-week follow-up

  2. Device Usability Using the System Usability Scale

    Scores range from 0 to 100; > 70 represents acceptable usability.

    Measured: Baseline to 12-week follow-up

  3. Change in Triceps Surae Peak Torque

    Torque assessments of the plantar flexors will be performed using an isokinetic dynamometer. Participants will be asked to perform 3 maximal contractions.

    Measured: Baseline to 12-week follow-up

  4. Change in the Five Times Sit to Stand Test

    Participants were asked to sit in a chair with arms folded across their chest and stand five times consecutively as quickly as possible. The time it took to complete five chair rises was measured.

    Measured: Baseline to 12-week follow-up

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Apr 2022
  2. Study start30 May 2023
  3. Primary completion7 Feb 2024
  4. Study completion7 Feb 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Device feasibility
Allocation
Not applicable
Intervention model
Single group
Model description
Six patients with PAD will be asked to complete daily (90 min/day) home-based leg HT for 12 weeks using the newly developed system. Outcomes will be measured at baseline and at 12-week follow-up.
Masking
None (open label)
Enrolment
6 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05335161
Sponsor's protocol ID
IRB-2022-375
Status last verified
Aug 2025
First submitted
13 Apr 2022
Last updated
15 Aug 2025
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing Home-based leg heat therapy in people with Peripheral Arterial Disease and Intermittent Claudication, run by Purdue University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 15 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 15 Aug 2025). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Six-minute Walk Distance (time frame: Baseline to 12-week follow-up). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Aug 2025.

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