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Not yet recruiting NCT06982612

Glycemic Control Following Occupational Work in a Hot Environment

No phase Interventional Plasma Glucose Following Prolonged Heat Exposure

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Hot environment, Temperate condition.
Who it may be relevant to
Registry conditions: Plasma Glucose Following Prolonged Heat Exposure. Basic parameters: 18 years — 45 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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

  • Other Hot environment
    Participants exercising in a 36 degrees celsius environment
  • Other Temperate condition
    Participants exercising in a 18 degrees celsius environment

Primary outcome measures

  • Plasma glucose [Time frame: 8hours]
Secondary outcome measures (12)
  • Plasma insulin [Time frame: 8hours]
  • Plasma osmolality [Time frame: 8hours]
  • Plasma volume change [Time frame: 8hours]
  • Urine volume [Time frame: 8hours]
  • Body mass [Time frame: 8hours]
  • Urine specific gravity/osmolality [Time frame: 8hours]
  • Rectal temperature [Time frame: 8hours]
  • Blood pressure [Time frame: 8hours]
  • Respiratory gas exchanges [Time frame: 8hours]
  • Rate of perceived exertion [Time frame: 8hours]
  • Rate of thermal sensation [Time frame: 8hours]
  • Feelings of thirst, urge to urinate, GI comfort, and stomach bloatedness [Time frame: 8hours]

Eligibility criteria

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 exclusion criteria.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Crossover
Masking
Single blind
Primary purpose
Basic science

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06982612 · LEON21544

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗