ClinicalTrials.gg
RecruitingNCT07050264HSRUpdated May 26, 2026

The Effect of Simulated Burn Injury on Post Exercise Recovery in Hot Environments

An interventional study of Simulated burn injury via application of absorbent and impermeable material over 60% of the body in Burn Injury, Body Temperature Regulation and Cardiovascular Physiology, sponsored by University of Texas Southwestern Medical Center. Recruiting at 1 site in United States. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-26.

Sponsored by University of Texas Southwestern Medical Center · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Started Mar 2026; still recruiting 8 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
28
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 10 studies in Burns by University of Texas Southwestern Medical Center — 2 open to participants now, 2 under way, none of them phase 3. Burns · University of Texas Southwestern Medical Center.

Started
2026
the only one that year
No phase
5 of 10
1 open now
Registered
10th of 10
by date

Among the 10 studies in Burns by University of Texas Southwestern Medical Center, this one is the only one that started in 2026, is one of 5 with no phase, and was the 10th registered.

Burns

905 studies on the registry are indexed under Burns; 164 are open to participants now.

Browse Burns studies →

Open to participants now

2 of the 10 studies in Burns by University of Texas Southwestern Medical Center are open now, in 1 country. Recruiting first, the newest first:

By country, each count listing its studies:

All 2 open studies →

Where they have run

Who these studies take

Of the 84 Burns studies recruiting now, 38 (45%) set no upper age limit and 37 (44%) stop at 75 or younger; 17 take children under 18; 9 take healthy volunteers.

This study: 18 Years to 65 Years · all sexes · healthy volunteers too.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 10 studies in Burns by University of Texas Southwestern Medical Center, or all of them as a file.
02

Study summary

Burn survivors have difficulty thermoregulating due to reduced skin blood flow and sweating responses at the grafted sites. It has been previously shown that this impaired heat dissipation results in burn survivors experiencing higher core temperatures for a given exercise/environmental exposure compared to non-burned individuals. This also holds true with the use of simulated burn injury. When an absorbent material is applied to the skin over a desired amount of body surface area, it replicates a burn injury of the same size (i.e., simulated burn injury). A question that remains unknown is if this impaired thermoregulation in burn survivors would affect post-exercise core temperature recovery, i.e., do burn survivors recover slower than non-burned individuals upon stopping exercise. To that end, the primary objective of this project is to determine the rate at which body temperature and other markers of thermoregulation recover after a bout of exercise in the heat and if this response is different in the same individual with and without simulated burn injury.

03

Conditions studied

  • Burn Injury
  • Body Temperature Regulation
  • Cardiovascular Physiology

Browse trials for

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 18 and 65 years of age
  • free of any significant underlying medical problems based upon a detailed medical history and physical exam, and normal resting .

Exclusion criteria

Exclusion Criteria:

  • Known heart disease
  • other chronic medical conditions requiring regular medical therapy including cancer, diabetes, neurological diseases, and uncontrolled hypertension, etc. as well as serious abnormalities detected on routine screening.
  • Individuals who are pregnant, planning to become pregnant, or breastfeeding will be excluded, this will be confirmed in females using a urine pregnancy test.
  • Taking prescribed medications (such as beta blockers and non-dihydropyridine calcium channel blockers) or over-the-counter medications that have known influences on thermoregulatory response.
  • Current smokers, as well as individuals who regularly smoked within the past 3 years.
  • is ≥ 31 kg/m2.
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
28 participants (estimated)

Study arms

  • Experimental
    Hot and Humid with simulated burns

    Individuals will be exposed to hot and humid conditions with a simulated burn injury.

    Other: Simulated burn injury via application of absorbent and impermeable material over 60% of the body

  • No intervention
    Hot and Humid without simulated burns

    Individuals will be exposed to hot and humid conditions without a simulated burn injury.

  • Experimental
    Hot and Dry with simulated burns

    Individuals will be exposed to hot and dry conditions with a simulated burn injury.

    Other: Simulated burn injury via application of absorbent and impermeable material over 60% of the body

  • No intervention
    Hot and Dry without simulated burns

    Individuals will be exposed to hot and dry conditions without a simulated burn injury.

Interventions

  • OtherSimulated burn injury via application of absorbent and impermeable material over 60% of the body

    Simulated burn injury via application of absorbent and impermeable material over 60% of the body

06

What researchers measure

Primary outcomes

  1. Core Temperature

    Time frame: From baseline to end of 60 minutes of recovery

Secondary outcomes

  1. Heart Rate

    Time frame: From baseline to the end of 60 minutes of recovery

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Mar 2026 (actual). Primary completion is estimated for Aug 2028, 29 months after the start.

Of 210 non-industry interventional studies with no phase under Burns, half reached primary completion within 18 months of starting (the median), counting those still running; a quarter within 6 and three quarters within 38. This study's planned 29 months is above that.

Counting every sponsor, half of 239 studies reached it within 15 months; a quarter within 6 and three quarters within 38.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 25, 2025
First posted
Jul 3, 2025
StartActual
Mar 1, 2026
Primary completionEst.
Aug 1, 2028
CompletionEst.
Aug 1, 2028
Last update
May 26, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 26, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07050264
Responsible party
Craig Crandall (Professor of Internal Medicine and director of the thermal and vascular physiology lab, University of Texas Southwestern Medical Center) — Principal investigator
First posted
Jul 3, 2025
Start date
Mar 1, 2026
Primary completion
Aug 1, 2028 (estimated)
Completion
Aug 1, 2028 (estimated)
Last update
May 26, 2026

Study contacts

Erin M Harper, B.S.
Contact
erin.harper2@utsouthwestern.edu
12143454737
Elizabeth A Gideon, PhD
Contact
betsygideon@texashealth.org
Craig G Crandall, PhD
principal investigator · University of Texas Southwestern Medical Center

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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