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Long COVIDHEALNCT06928116

Heat thErapy And mobiLity in COVID-19 Survivors

A study testing Heat therapy and Walking in people with Long COVID, run by University of Nebraska at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Post-acute sequelae of SARS-CoV-2 infection (PASC) is becoming a major risk factor for chronic diseases, with older adults and those with underlying health conditions at risk of developing persistent mobility limitations and disabilities. Read more about this study

Who is it for?
Ages 50 to 90 years
Conditions the study is for
Long COVID
What is being tested?
Heat therapy and Walking
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
99 participants
Where
1 siteUnited States
Study dates
16 Jan 2025to Aug 2029
Phase
Interventional
Are there results?
Not yet: the study is under way

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 50 to 90 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Between the ages of 50 and 90 years
  • Free from orthopedic limitations that would prohibit performing leg exercise
  • BMI < 40 kg/m2 and weigh < 400lbs
  • Previously contracted Covid-19 and have persistent symptoms such as a fatigue or decline in physical function, for at least 2 months following SARS-CoV-2 infection

Who cannot join

  • Unable to give written informed consent
  • Women who are pregnant, breastfeeding, or likely to become pregnant within the next 6 months
  • Claustrophobia
  • Orthopedic limitations that would prohibit them from walking
  • Currently enrolled in an exercise-based or respiratory muscle rehabilitation program.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Gwenael Layec, PhD contact

402-554-3779

unovrl@unomaha.edu

United States1 site, 1 recruiting
  • University of Nebraska Omaha

    Omaha, Nebraska, 68182

    Gwenael Layec, PhD, 402-554-3779, unovrl@unomaha.edu

    Recruiting

Other trials in United States

About this study

Official title: Physical Rehabilitation of Long COVID by Heat Therapy

Post-acute sequelae of SARS-CoV-2 infection (PASC) is becoming a major risk factor for chronic diseases, with older adults and those with underlying health conditions at risk of developing persistent mobility limitations and disabilities. Although exercise intervention is a common strategy to restore functional capacity, it may not be feasible or enticing to many people with PASC. This clinical trial seeks to establish the tolerability and efficacy of at home lower-body heat therapy for improving functional capacity along with metabolic and vascular health in late-middle aged and older adults with PASC, also known as "long COVID".

Read the detailed description

Post-acute sequelae of SARS-CoV-2 infection (PASC) affects 5 out of 10 patients hospitalized for the coronavirus disease 2019 (COVID-19) and ~11% of all adults infected by SARS-CoV-2, which makes this condition a growing public health concern. It is associated with important disabilities, cognitive dysfunction, and increased risks for cardiovascular and metabolic diseases. Although exercise-based intervention is a promising rehabilitation strategy, participation rates are commonly low in clinical population. In addition, post-exertional malaise, a common symptom with PASC, is a major safety concern in these patients, which may prevent a significant proportion of these individuals to receive adequate rehabilitation. In this context, there is a critical need to develop well-tolerated and effective strategies at home that ameliorates health and functional capacity in individuals with PASC. One promising approach that offers numerous health benefits is whole-body heat therapy. Whether this intervention is effective when confined to the lower body and well tolerated at home in people with PASC is, however, unknown.

The overall objective of this project is to determine the safety, tolerability, and efficacy of home-based lower body heat therapy in late middle-age and older adults with PASC. Investigators will test the central hypothesis that home-based lower body heat therapy is safe, well adhered, and can improve functional capacity and several surrogate markers for metabolic and vascular health in late-middle age and older adults with PASC. Specific Aim 1 will test the hypothesis that lower body heat therapy at home is safe, well adhered, and improve both cognitive and physical function in middle-age and older adults with PASC. Selected participants will be randomly allocated to perform 8 weeks of home-based lower body heat therapy (HT, skin temperature 38-40˚C, 40-55 min, 5 per week at home), a thermoneutral condition (CT, skin temperature 33˚C, same duration and frequency), or a walking intervention using wearable technology (WT, 1,500-3,000 additional steps from baseline, 3-5 days per week). We will compare the 6 min walking distance, the short physical performance battery test score, gait speed, cognitive function, incidence of adverse events, and participant's adherence to intervention between groups. Specific Aim 2 will test the hypothesis that heat therapy will attenuate inflammation, which will then decrease arterial stiffness, and improve both vascular endothelial function and muscle intracellular oxygen availability in participants with PASC. Investigators will use in vitro assays on blood samples and Doppler ultrasound techniques to assess changes in inflammation, redox status, pulse-wave velocity, and flow-mediated dilation. Muscle intracellular oxygen availability will be measured by magnetic resonance spectroscopy in vivo. Specific Aim 3 will test the hypothesis that lower body heat therapy will improve glucose control as a result of enhanced mitochondrial function. All these effects will not be statistically inferior to the WT group. The proposed research is highly significant as it is easily translatable and is expected to guide future rehabilitation strategies to mitigate long-term disabilities in patients with PASC.

Conditions
Long COVID
Being tested
Heat therapy, Sham Control, Walking
Keywords
Heat Therapy, mobility limitations, Post-acute sequelae of SARS-CoV-2 infection (PASC)
Medical subject headings
Post-Acute COVID-19 Syndrome, Hyperthermia, Mobility Limitation

What participants receive

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

  • Heat therapyBehavioural

    At home lower body heat therapy

  • Sham ControlBehavioural

    Sham Thermoneutral

  • WalkingBehavioural

    Walking intervention

Study groups in NCT06928116
Study groupRoleWhat they receive
Heat TherapyExperimentalAt home heat therapy 5 times (40-55 min) per week for 8 weeks.
Receives: Behavioral: Heat therapy
Control TherapySham comparatorSham at home thermoneutral therapy 5 times (40-55 min) per week for 8 weeks.
Receives: Behavioral: Sham Control
Walking Intervention Using Wearable TechnologyActive comparator+1,500-3000 steps per day 3-5 days a week for 8 weeks.
Receives: Behavioral: Walking

What is being measured

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

  1. 6 min walking distance

    Distance covered during 6 min of walking

    Measured: 8 weeks

  2. Short Physical Performance Battery Test

    Test of physical functional capacity

    Measured: 8 weeks

  3. Arterial stiffness

    Pulse Wave velocity

    Measured: 8 weeks

Timeline

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

  1. First posted15 Apr 2025
  2. Study start16 Jan 2025
  3. Primary completion31 Aug 2028 (estimated)
  4. Study completionAug 2029 (estimated)

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 N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
99 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06928116
Sponsor's protocol ID
0550-24-FB
Other IDs
R01AG089307
Acronym
HEAL
Status last verified
Aug 2026
First submitted
9 Apr 2025
Last updated
28 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: The de-identified data will be deposited into a Data Repository specific to biomedical sciences using standard rights waivers as those established by Open Data Commons (ODC)

Questions about this trial

What is this clinical trial studying?

A study testing Heat therapy and Walking in people with Long COVID, run by University of Nebraska 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 4 inclusion and 5 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: looking for participants now, as of the sponsor's last update on 28 Sep 2026. 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. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

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

Contact Gwenael Layec, PhD (402-554-3779, unovrl@unomaha.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

6 min walking distance (time frame: 8 weeks). The study lists 3 primary outcomes in all. 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 28 Sep 2026; AzTrials last refreshed its copy on 26 Oct 2026.

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