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Glycemic Control Following Occupational Work in a Hot Environment

Glycemic Control Following Occupational Work in a Hot Environment

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06982612
Enrollment
20
Registered
2025-05-21
Start date
2025-05-31
Completion date
2026-10-01
Last updated
2025-05-21

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

Conditions

Plasma Glucose Following Prolonged Heat Exposure

Keywords

heat, plasma glucose, worker, glycemia, OGTT

Brief summary

Occupational workers regularly perform physically demanding tasks in hot environments, exposing them to heat stress and potential dehydration. While the physiological impacts of heat exposure are well-documented, its effects on glycemic control remain less understood. Given the rising global temperatures due to climate change and the increasing prevalence of metabolic disorders such as obesity and type 2 diabetes, it is essential to investigate how heat exposure during work influences glycemic regulation. Understanding these interactions will help inform future occupational health guidelines and metabolic health recommendations in physically demanding industries.

Interventions

Participants exercising in a 36 degrees celsius environment

OTHERTemperate condition

Participants exercising in a 18 degrees celsius environment

Sponsors

Loughborough University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Randomised, crossover design

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Male or female * Generally fit and healthy * Participate in endurance or intermittent exercise at least 3 times a week or minimum of 150 minutes moderate intensity activity per week

Exclusion criteria

* Under 18 or 45 and over, * any morbidity or medication that might influence carbohydrate/fat metabolism (i.e., liver/renal/cardiovascular disease) or cycling ability (musculoskeletal injury etc), * coagulation or bleeding disorders, * blood-borne illness, * heart conditions, * congenital heart disease, * uncontrolled exercise-induced asthma, * smoking (including vaping), * allergies to the products used in the study, * dieting or restrained eating behaviours. * Females with amenorrhea would be an

Design outcomes

Primary

MeasureTime frameDescription
Plasma glucose8hoursMeasured using colorimetric assay from venous blood samples

Secondary

MeasureTime frameDescription
Urine specific gravity/osmolality8hoursDetermined from urine samples collected before and after exercise
Rate of perceived exertion8hoursusing Borg scales (from 6 \[no effort\] to 20 \[maximal effort\])
Rate of thermal sensation8hoursusing -10 \[cold\] to +10 \[hot\] scale.
Feelings of thirst, urge to urinate, GI comfort, and stomach bloatedness8hoursusing scales (0 = no feeling, 10 = extreme feeling)
Plasma insulin8hoursMeasured using ELISA from venous blood samples
Plasma osmolality8hoursMeasured using freezing point depression from venous blood samples
Plasma volume change8hoursDetermined from haemoglobin and haematocrit measures in blood samples
Urine volume8hoursDetermined from urine samples collected before and after exercise
Body mass8hoursDetermined from weighing participants before and after exercise
Rectal temperature8hoursMeasured via rectal probe
Blood pressure8hoursMeasured via and automated sphygmomanometer
Respiratory gas exchanges8hoursMeasured via Douglas bag, gas content and volume

Other

MeasureTime frameDescription
Stroop test8hoursThe Stroop Test is a psychological assessment that measures a person's ability to inhibit cognitive interference and control attention. Typically, it involves naming the color of the ink in which a word is printed, even when the word itself names a different color (e.g., the word red printed in blue ink). The delay in response time when the word and ink color do not match-known as the Stroop effect-reflects the difficulty of suppressing automatic cognitive processes.
Go/no-go task for response inhibition (cognitive function)8hoursParticipants will be instructed to press the space bar when a green image appears onscreen (go stimulus) and to inhibit responding when a red image is presented (the no-go stimulus). Increased commission error responses (i.e. responding incorrectly on a no-go trial) will indicate reduced response inhibition. Commission errors and correct responses will be measured as indices of performance.
N-back task for working memory (cognitive function)8hoursThe task will comprise three progressively harder memory loads (1-Back, 2-Back, 3-Back). Each stimulus type will be used in all memory loads. Participants will have to respond using the space bar when they see a stimulus that is presented one, two, or three steps previously, dependent on the load condition.

Contacts

Primary ContactStephen A Mears, PhD
s.a.mears@lboro.ac.uk+44 1509 226391

Outcome results

None listed

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