Skip to content

Sweat Response, Sweat Composition and Thermoregulatory Response to Exercise in Heat in Adults With Cystic Fibrosis on Modulator Therapy.

A Study to Assess the Sweat Response, Sweat Composition and Thermoregulatory Response to Exercise in Heat in Adults With Cystic Fibrosis on Cystic Fibrosis Transmembrane Conductance Regulator Modulator Therapy Compared Healthy Controls.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05896488
Acronym
Sweat-CF
Enrollment
18
Registered
2023-06-09
Start date
2023-03-18
Completion date
2024-03-18
Last updated
2023-06-09

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

Conditions

Cystic Fibrosis

Keywords

Exercise, CFTR modulator therapy, thermoregulation, heat-related illness, sweat sodium

Brief summary

Cystic fibrosis (CF) is a common inherited condition in the Caucasian population resulting in poor function and/or production of the CF transmembrane conductance regulator (CFTR) protein. The CFTR protein plays a crucial role in the secretion and re-absorption of sodium chloride within the sweat gland. The sweat gland has played a key role in diagnosing and understanding CF with sweat chloride elevation being a key criterion to diagnosing CF. People with CF are thought to be at risk of exertional heat illness during exposure to hot environments or during prolonged periods of exercise and are currently encouraged to take salt supplements during periods of excessive sweating. Kaftrio®, a newly approved pharmacological therapy has shown a rapid and sustained reduction in sweat chloride levels on initiation of this treatment. This study will aim to play a crucial part in understanding the sweat response, sweat composition and the thermoregulatory response to exercise in the heat in people with CF on Kaftrio®.

Detailed description

Cystic fibrosis (CF) is a common inherited condition in the Caucasian population, affecting approximately 52, 246 people in Europe. Mutations in the CF transmembrane conductance regulator (CFTR) gene results in poor function or production of the CFTR protein which functions as an anion channel to transport ions across the cell membrane. The sweat gland has played a substantial part in diagnosing and understanding CF with sweat chloride elevation being a key criterion to diagnosing CF. Traditionally, abnormal function of the CFTR protein in the sweat gland results in failure to reabsorb sodium chloride leading to excessive salt loss. People with CF are thought to be at risk of exertional heat illness during exposure to hot environments or during prolonged periods of exercise and are currently encouraged to take salt supplements during periods of excessive sweating. Over the last decade pharmacological therapies (CFTR modulator therapies (CFTRm)) which target the underlying cellular defect characterising CFTR in people with CF have been developed. Kaftrio® is now the most widely used modulator therapy. Studies have shown a rapid and sustained reduction in sweat chloride levels on initiation of these highly effective CFTRm. The need for salt supplementation may be influenced when taking CFTRm. Therefore, there is a need to further understand the sweat response relative to the needs in people with CF. This study will recruit 9 people with CF who currently taking Kaftrio® and 9 healthy age-, sex- and weight-matched controls who are ≥ 18 years old. We will ask all participants to attend the laboratories for 2 visits. Visit 1 is designed to calculate metabolic heat production during different cycling intensities in order to set the workload for visit 2 relative to their metabolic heat production. Visit 2 is designed to collect sweat and thermoregulatory indices during 1 hour of cycling in the heat. This study will compare the sweating and thermoregulatory response to exercising in the heat in a group of people with CF who are stable on Kaftrio® compared to a healthy matched control group. The aims of this study are to: 1. Determine the sweat sodium concentration in adults with CF on Kaftrio® from exercise at a fixed-rate of metabolic heat production under heat stress conditions and whether this is different to healthy age- weight- and sex- matched controls; 2. Determine the local and whole-body sweat rate in adults with CF on Kaftrio® during exercise under heat stress conditions and whether this is different to healthy age- weight- and sex- matched controls; 3. Determine how adults with CF on Kaftrio® respond in terms of skin blood flow during exercise under heat stress conditions and whether this is different to healthy age- weight- and sex- matched controls; 4. Determine thermal strain from skin and core body temperature in adults with CF on Kaftrio® during exercise under heat stress conditions and whether this is different to healthy age- weight- and sex- matched controls.

Interventions

None listed

Sponsors

University Hospital Southampton NHS Foundation Trust
CollaboratorOTHER
University of Portsmouth
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

for participants with CF: * Is taking CFTRm * Males and females ≥ 18 years of age * CF diagnosis based on clinical features, supported by a history of an abnormal sweat test (sweat \[Cl-\] \> 60 mmol·L-1 \> 100 mg sweat), where possible, diagnostic genotyping would also be desired * Can clearly state that they are not pregnant * No contraindications to performing exhaustive exercise * Can understand and cooperate with the study protocol * No exacerbation (increase in cough, sputum or breathlessness, or change in the colour of sputum) within the preceding 2 weeks * No weight loss in the preceding 2 weeks Inclusion Criteria for healthy control participants: * Healthy males and females who are age- weight- and sex- matched to the enrolled individuals with CF * Can clearly state that they are not pregnant * No clinical diagnosis of a chronic disease * Can understand and cooperate with the study protocol * No contraindications to performing exhaustive exercise

Exclusion criteria

for participants with CF: * Any non-pulmonary conditions that may impair exercise ability, such as musculoskeletal disorders (arthritis, joint or muscle disease) and cardiovascular disease (congenital heart disease or cardiomyopathy). * Unstable co-morbid asthma (daily pulmonary function variability of \>20%) * Is pregnant during the initial screening process * Unable to understand or cooperate with the study protocol due to learning difficulties or otherwise * Not of a suitable age for testing * Is a smoker or inhales any other substances

Design outcomes

Primary

MeasureTime frameDescription
Sweat sodium concentration (mmol∙L-1)Day 2 - baselineBetween group differences in sweat sodium concentration

Secondary

MeasureTime frameDescription
Forearm sweat rate (mg∙min-1∙cm2)Day 2 - baselineBetween group differences in forearm sweat rate
Mid-back sweat rate (mg∙min-1∙cm2)Day 2 - baselineBetween group differences in mid-back sweat rate
Sweat gland activity (gland∙cm2)Day 2 - baselineBetween group differences in sweat-gland activation derived from the modified-iodine patch technique
Core temperature (°C)Day 2 - baselineBetween group differences in core temperature derived from rectal temperature
Mean skin temperature (°C)Day 2 - baselineBetween group differences in skin temperature
Heart rate (b∙min-1)Day 2 - baselineBetween group differences in heart rate
Cutaneous blood fluxDay 2 - baselineBetween group differences in cutaneous blood flux
Whole-body sweat rate (mL)Day 2 - baselineBetween group differences in whole-body sweat rate derived from pre - post nude body mass
Perception of temperature sensationDay 2 - baselineBetween group differences in perception of temperature sensation
Perception of thermal comfortDay 2 - baselineBetween group differences in perception of thermal comfort
Change in thermal comfortDay 2 - baselineBetween group differences in change in thermal comfort
Rate of change in thermal comfortDay 2 - baselineBetween group differences in rate of change in thermal comfort
Heat sensitivityDay 2 - baselineBetween group differences in heat sensitivity derived from sweat rate / change in thermal comfort
Heat illness symptom indexDay 2 - baselineBetween group differences in heat-related illness symptoms
Maximal oxygen uptake (VO2 max)Day 1 - baselineBetween group differences in oxygen uptake derived from a maximal cardiopulmonary exercise test
Urine osmolality (mOsmol/kg)Day 2 - baselineBetween group differences in urine osmolality

Countries

United Kingdom

Contacts

Primary ContactZoe Saynor
zoe.saynor@port.ac.uk02392843080
Backup ContactLauren Clayton
lauren.clayton@port.ac.uk02392843085

Outcome results

None listed

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