Hyperthermia

16

Review clinical trials related to Hyperthermia. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Work Design Interventions for Older Workers During Consecutive Days in the Heat

The goal of this project is to compare different ways to schedule a workday to see if older workers should follow a specific work protocol to reduce strain on the heart and muscles across two consecutive days of work. Participants will come to the lab a total of six times. During four of the visits participants will complete a box carrying task, simulating unloading a delivery truck. This will take place in a hot and humid room to simulate being outdoors during the summer.

Participants needed: 32
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: State University of New York at BuffaloUpdated: Jun 30, 2026
Eligibility criteria

Healthy individuals [+3]

History of cardiovascular, metabolic, respiratory, neural, or renal disease [+6]

Status: Not yet recruiting

Work Design Interventions for Heat Resilience

The goal of this project is to compare different ways to schedule a workday to see if older workers should follow a specific work protocol to reduce strain on the heart and muscles. Participants will come to the lab a total of six times. During four of the visits participants will complete a box carrying task, simulating unloading a delivery truck. This will take place in a hot and humid room to simulate being outdoors during the summer.

Participants needed: 32
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: State University of New York at BuffaloUpdated: Jun 30, 2026
Eligibility criteria

Healthy individuals [+3]

History of cardiovascular, metabolic, respiratory, neural, or renal disease [+6]

Status: Not yet recruiting

Hyperthermia in Patients With Chronic Primary Pain - Effects on Thermoregulation, Somatosensory System and Movement Evoked Pain

This study, in a quasi-experimental matched two-group pre-post design, investigates the effect of serial water-filtered whole-body hyperthermia on circadian core body temperature, the somatosensory system (nociception) and the movement evoked pain in healthy and patients with chronic primary pain (e.g., fibromyalgia). The intervention lasts 3 weeks with two treatment sessions per week.

Participants needed: 60
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Bern University of Applied SciencesUpdated: Jun 2, 2026Locations: 1
Eligibility criteria

Confirmed diagnosis of widespread pain (ICD-11 MG30.01) [+9]

Participation in other clinical studies [+7]

Status: Not yet recruiting

Laboratory Heat Biomarker and Cooling Interventions

Our study has two goals. The first goal is to find a blood test that can detect signs of strain from heat in the body ("a biomarker"). Second, the study team wants to identify types of devices that can help people cool down quickly. By identifying biomarkers for heat strain, scientists can better track and treat the health effects of heat. The study team will identify such biomarkers by simulating, in a laboratory-based environment, the heat and physical work that real-world workers experience. In addition, the study team plans to test two cooling technologies that might keep people cool during physical activity.

Participants needed: 30
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: Stanford UniversityUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Age 18-50 [+4]

Cannot provide informed consent [+9]

Status: Recruiting

IEEM-Heat and Heart Failure

We will test the hypothesis that increasing skin wetness, and thus evaporative cooling, will attenuate the increase in core body temperature and accompanying cardiac stress during heat wave conditions in individuals with congestive heart failure. Secondly, we propose that wearing a water-saturated T-shirt will also be beneficial to attenuate the increase in core body temperature and accompanying cardiac stress during heat wave conditions in individuals with congestive heart failure. To accomplish these objectives, individuals with congestive heart failure and otherwise healthy control individuals will be exposed to the simulated heat wave condition (hot and dry) with the following cooling modalities: A) control trial (no limb immersion or skin wetting), B) skin wetting only trial, and C) water-saturated T-shirt trial in a randomized crossover fashion. Thermoregulatory and cardiovascular responses will be evaluated throughout these simulated heat wave exposures. Primary outcomes variables will be skin and core temperatures, while secondary variables will include measures of cardiovascular stress, myocardial perfusion, heart rate, and echo-based measures of cardiac function.

Participants needed: 88
Trial details
Age: 45+Biological sex: AllType: InterventionalSponsor: University of Texas Southwestern Medical CenterUpdated: May 26, 2026Locations: 1
Eligibility criteria

Participants must be free of any significant underlying medical problems based u...

Known heart disease; other chronic medical conditions requiring regular medical...

Status: Recruiting

Title: ICARUS - Psycho-physiological Profiling of Low and High Heat-resilient Individuals

The escalating environmental heat-stress associated with global warming is a societal challenge with large and potential harmful consequences for humans. Excess morbidity and mortality during heat waves provides strong evidence for fatal outcomes. However, it is unclear why some people are particularly vulnerable and get sick from hyperthermia, while others adapt and tolerate exposure. The Icarus project aims to provide a psycho-physiological framework for improved mitigation of the health threats associated with global warming. Combining expertise in integrative thermal physiology, pharmacology, photobiology, psychology and machine learning, we will collaborate on comprehensive cross-scientific studies using controlled lab-exposure combined with investigations in ecological settings including vulnerable and highly tolerant people across populations from northern to southern Europe. Advanced algorithms will be developed to generate personalized alerts and advising based on behavioral patterns, psychological profiling, predicted vulnerability and willingness to adopt resilience-building strategies. Global warming is projected to continue towards the end of the 21st century and constitutes an increasing threat to human health unless we as individuals and collectively become better in preventing acute effects, as well as devise sustainable strategies to limit further anthropogenic warming of the climate system. Acutely, improved guidance is important for both individual and public health, where Icarus aims at providing a highly improved basis for preventing heat-related disease, advising or nudging people towards pro-health behavior, including smarter use of technologies to mitigate heat stress, or adjusting medication to reduce adverse effects during heat events. In support of the sustainability agenda, our framework also forms a novel basis for developing advising algorithms relevant for optimization of climate change mitigation policy-making.

Participants needed: 80
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: University of ThessalyUpdated: Apr 3, 2026Locations: 2
Eligibility criteria

Age 18-65 years (or your protocol-specific age range) [+6]

History of cardiovascular, metabolic, neurological, or dermatological disease [+8]

Status: Recruiting

The Effectiveness of Emergency Room Protocols for Treating Hyperthermia

This study will help us as scientists and clinicians understand how effective commonly used cooling protocols in emergency departments are and which of the protocols is the most effective. It consists of a single, approximately 1 hour preliminary session and five, approximately 3 hour experimental sessions, equaling an approximate 16 hour total time commitment. The purpose of this research is to test the effectiveness of three cooling protocols. 1. Cooling packs 2. "Ice Sheets", which are bed sheets soaked in ice water, wrapped around the participant, while a fan blows air on them. 3. Body bag filled with ice, commonly used in emergency departments to treat hyperthermia Additionally, a negative control (passive cooling in air-conditioned room) and a positive control (cold water immersion).

Participants needed: 50
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: University of Colorado, Colorado SpringsUpdated: Feb 25, 2026Locations: 1
Eligibility criteria

Active, healthy individuals

Pregnant or planning on becoming pregnant [+4]

Status: Recruiting

Predicting Responses to Exhausting, Prolonged, And Repeated Exercise Demands (PREPARED) for Heat

The overall goal of this project is to identify a work/rest cycle that allows for faster mission completion needed in emergency situations, compared to current Army heat guidance, while mitigating heat strain and neuromuscular fatigue. This project will determine the trade-off between faster mission completion and risk of heat strain and physical performance decrements. Completion of this project will allow military leaders to make informed decisions by understanding the impact of their choices on the magnitude of physical performance decrements and expected heat casualties, setting up hot weather missions for success.

Participants needed: 24
Trial details
Age: 18-39Biological sex: AllType: InterventionalSponsor: State University of New York at BuffaloUpdated: Jan 26, 2026Locations: 1
Eligibility criteria

Healthy individuals [+1]

History of cardiovascular, metabolic (such as clinical thyroid disease), respira... [+8]

Status: Recruiting

Heat Waves and the Elderly - Cooling Modalities

The purpose of this study is to assess how well cooling modalities work in reducing cardiovascular stress of the elderly to heat wave conditions

Participants needed: 100
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: University of Texas Southwestern Medical CenterUpdated: Oct 23, 2025Locations: 1
Eligibility criteria

65 years of age or older [+1]

Known heart disease [+5]

Status: Recruiting

Postoperative Re-irradiaTion With and Without HYPERthermia: Toxicity, Quality of Life and Survival in Patients With Locoregional Recurrent Breast Cancer

In the Netherlands, breast cancer patients with locoregional recurrence (LRR) and high-risk factors are treated with postoperative re-irradiation with or without hyperthermia. Retrospective studies showed that 3-year locoregional control after postoperative re-irradiation with hyperthermia was 68-83%, and severe toxicity in up to 40% of LRR patients. Unfortunately, no prospective (randomized) data are available on clinical outcomes. Consequently, variation exists in hyperthermia-treatment and re-irradiation schedules. Prospective real-world data on oncological outcomes, toxicity and quality of life is highly needed for shared decision-making between patients and professionals. These data will be used in the design of a future randomized trial comparing postoperative re-irradiation and hyperthermia-treatment in high-risk LRR patients.

Participants needed: 500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Amsterdam UMC, location VUmcUpdated: Oct 6, 2025Locations: 1
Eligibility criteria

WHO performance scale ≤2 [+8]

Diagnosed with primary breast sarcoma [+1]

Status: Recruiting

IEEM- Work:Rest Cycles in Burn Survivors- Humidity

The purpose of this project is to identify the effects of a severe burn injuries in humans on core temperature responses during work:rest cycles while in a heated environment.

Participants needed: 70
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: University of Texas Southwestern Medical CenterUpdated: Aug 26, 2025Locations: 1
Eligibility criteria

Participants must be free of any significant underlying medical problems based u...

Known heart disease; other chronic medical conditions requiring regular medical...

Status: Not yet recruiting

Analysis of Hyperthermia as an Adjunctive Treatment to Evidence-based Clinical Intervention in Subjects With Plantar Fasciitis: a Double-blind Randomized Clinical Trial

This project aims to analyze the use of hyperthermia within a treatment protocol for plantar fasciitis, as well as to determine the difference between two and three sessions per week. Study participants will be divided into four intervention groups: the first will receive two sessions per week for a period of six months, while the second will receive three sessions per week for the same period. The treatment protocol will consist of therapeutic physical exercise focused on the foot muscles and stretching the plantar fascia and posterior chain, hyperthermia on the plantar fascia insertion area in the calcaneus and adjacent areas, and the use of an orthotic insole used for walking. The third and fourth intervention groups will receive the same treatment as mentioned above, but without hyperthermia. The third group will receive three sessions per week, while the second group will receive two sessions per week. Two different types of measurement variables will be used: objective variables will be used to measure local pain using an algometer, assess ankle joint range of motion, and use ultrasound imaging techniques. Subjective variables will also be used through validated questionnaires, which will address physical activity, perceived functional limitations in patients with lower limb pathologies, lower limb functional assessment, and a visual analogue scale for pain perception.

Participants needed: 64
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: University of MalagaUpdated: Aug 5, 2025
Eligibility criteria

Have a diagnosis confirmed by performing an ultrasonography of Plantar Fascitis [+1]

Have undergone surgery. [+3]

Status: Not yet recruiting

Analysis of Hyperthermia as an Adjunctive Treatment to Evidence-based Clinical Intervention in Subjects With Bursitis: a Double-blind Randomized Clinical Trial

This project aims to analyze the use of hyperthermia within a bursitis treatment protocol, as well as to determine the difference between two and three sessions per week. Study participants will be divided into four intervention groups: the first will receive two sessions per week for a period of six months, while the second will receive three sessions per week for the same period. The treatment protocol will consist of therapeutic physical exercise focused on the affected joint, stretching of the involved muscles, and the application of hyperthermia to the bursa and surrounding areas. The third and fourth intervention groups will receive the same treatment as mentioned above, but without hyperthermia. The third group will receive three sessions per week, while the second group will receive two sessions per week. Two different types of measurement variables will be used: on the one hand, the objective variable will be measurement and assessment of the bursa using ultrasound imaging. Subjective measurement variables will also be used through validated questionnaires, which will address physical activity, perceived functional limitations, and the visual analog scale for pain perception.

Participants needed: 120
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: University of MalagaUpdated: Aug 1, 2025
Eligibility criteria

Have a diagnosis confirmed by performing an imaging test of Bursitis [+1]

Have undergone surgery. [+3]

Status: Not yet recruiting

Analysis of Hyperthermia as a Complementary Treatment to Evidence-based Clinical Intervention in Subjects With Carpal Tunnel Syndrome:

This project aims to analyze the use of hyperthermia within a treatment protocol for Carpal Tunnel Syndrome (CTS), as well as to determine the difference between two and three sessions per week. Study participants will be divided into four intervention groups: the first will receive two sessions per week for a period of six months, while the second will receive three sessions per week for the same period. The treatment protocol will consist of therapeutic physical exercise focused on the hand flexor muscles and neural stretching, the application of hyperthermia to the carpal tunnel and adjacent areas, and the use of a night splint. The third and fourth intervention groups will receive the same treatment as mentioned above, but without hyperthermia. The third group will receive three sessions per week, while the second group will receive two sessions per week. Two different types of measurement variables will be used: objective variables will be used to measure hand flexor muscle strength and wrist free range of motion. Subjective variables will also be used through validated questionnaires covering physical activity, perceived functional limitations, upper limb functional assessment, neuropathic pain, and a visual analogue scale for pain perception.

Participants needed: 160
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: University of MalagaUpdated: Apr 24, 2025
Eligibility criteria

Have a diagnosis confirmed by performing an electromyography of Carpal Tunnel Sy... [+1]

Have undergone surgery. [+3]

Status: Recruiting

Impact of Extreme Heat on Myocardial Blood Flow and Flow Reserve in Young and Older Adults

Extreme heat causes a disproportionate number of hospitalizations and deaths in older adults relative to any other age group. Importantly, many hospitalizations and deaths are primarily due to cardiovascular events such as myocardial infarction. Previous data indicate that older adults have attenuated skin blood flow and sweating responses when exposed to heat, resulting greater increase in core body temperature. Despite these observations, relatively little is known about the risk for myocardial ischemia potentially contributing to the aforementioned higher morbidity and mortality in older adults during heat waves. The broad objective of this work is to determine the impact of ambient heat exposure on myocardial blood flow and flow reserve in young and older adults. Aim 1 will test the hypothesis that older adults exhibit attenuated myocardial flow reserve compared to young adults during heat stress. Aim 2 will determine if the percent of maximal myocardial flow reserve (assess via vasodilator stress) during heat exposure is higher in older adults compared to young adults. The expected outcome from this body of work will improve our understanding of the consequences of aging on cardiovascular responses to ambient heat stress.

Participants needed: 24
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of Texas Southwestern Medical CenterUpdated: Feb 24, 2025Locations: 1
Eligibility criteria

Healthy male and female individuals [+2]

Known heart disease; other chronic medical conditions requiring regular medical... [+5]

Status: Recruiting

Prospective Hyperthermia Database in Cancer Patients (HT Register)

This monocentric study registry records all cancer patients at the Charité which are treated with hyperthermia to examine the therapeutic use of hyperthermia in cancer patients in the general application and to obtain an accurate risk-benefit balance After confinement in this database are the patients prospectively in order to complications, disease status and survival status tracked. Furthermore there is the possibility in the course of this study to an optional take part in translational accompanying research with the aim of prognostic factors for response to hyperthermia treatment.

Participants needed: 1,000
Trial details
Biological sex: AllType: ObservationalSponsor: Pirus GhadjarUpdated: Aug 15, 2023Locations: 2Duration: 10 Years
Eligibility criteria

Contrazeption with female patients at the capable of bearing children age [+3]

Exclusion criteria for the hyperthermia (such as hip prosthesis in the therapeut... [+1]