Skip to content

Skin Wetting in Burn Survivors

Skin Wetting in Burn Survivors

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06529757
Enrollment
40
Registered
2024-07-31
Start date
2024-07-31
Completion date
2026-07-31
Last updated
2025-10-21

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

Conditions

Burn Injury

Brief summary

This project will identify the efficacy of whole body skin wetting aimed to attenuate excessive elevations in internal body temperatures during physical activity in well-healed burn survivors. The investigators will conduct a randomized crossover design study. Non-burned control subjects, subjects who experienced burns covering \ 20% to 40% of their body surface area, and subject having burns \>40% of their body surface area will be investigated. Subjects will exercise in heated environmental conditions while receiving no cooling or whole body skin wetting.

Interventions

Subjects will exercise for 60 minutes in the indicated environmental condition while being exposed to whole body skin wetting. Skin wetting will be performed by spraying water onto the whole body throughout the exercise bout.

OTHERNon-cooling

Subjects will exercise for 60 minutes in the indicated environmental condition while being exposed to no cooling modalities.

Sponsors

University of Texas Southwestern Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

Non-burn survivors * Healthy male and female subjects * 18-65 years of age. * Free of any underlying medical conditions

Exclusion criteria

(non-burned individuals): * Any burn-related injuries resulting in at least one night of hospitalization. * Heart disease or any other chronic medical condition requiring regular medical therapy including cancer, diabetes, and hypertension. * Abnormalities detected on routine screening * Individuals who participate in a structured aerobic exercise training program at moderate to high intensities. * Current smokers, as well as individuals who regularly smoked within the past 3 years. * Body mass index of greater than 30 kg/m\^2. * Pregnant individuals Inclusion Criteria (burn survivors): * Healthy male and female subjects * 18-65 years of age. * Free of any underlying medical conditions * Having a burn injury covering 20-40% or \>40% of the participant's body surface area; at least 50% of those burn injuries must be full thickness that required skin grafting. * Participants must have been hospitalized due to the burn injury for a minimum of 15 days

Design outcomes

Primary

MeasureTime frameDescription
Core TemperaturePrior to and throughout the bout of exercise; an average of 90 minutes.During exercise, one's core body temperature will increase. This device will measure this increase in core body temperature throughout the exercise.

Secondary

MeasureTime frameDescription
Mean Skin TemperaturePrior to and throughout the bout of exercise; an average of 90 minutes.Average skin temperature from six sites.
Rate Pressure ProductPrior to and throughout the bout of exercise; an average of 90 minutes.Obtained from heart rate and systolic blood pressure.
Whole body sweat rateBefore and after exercise. 2 min per measure.Whole body sweat rate will be measured from pre and post nude body mass measures.

Countries

United States

Contacts

Primary ContactCraig Crandall, PhD
craigcrandall@texashealth.org214-345-4623
Backup ContactErin Harper, BS
ErinHarper@texashealth.org214-345-4737

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026