Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12619001526167
Ethics application status
Approved
Date submitted
2/10/2019
Date registered
5/11/2019
Date last updated
14/07/2024
Date data sharing statement initially provided
5/11/2019
Type of registration
Prospectively registered

Titles & IDs
Public title
Investigating heat tolerance in females
Scientific title
Investigating heat tolerance in females
Secondary ID [1] 297248 0
None
Universal Trial Number (UTN)
U1111-1228-1871
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Heat illness 311320 0
Condition category
Condition code
Injuries and Accidents 313136 313136 0 0
Other injuries and accidents

Intervention/exposure
Study type
Observational
Patient registry
False
Target follow-up duration
Target follow-up type
Description of intervention(s) / exposure
The exposure variable in this study is exertional heat stroke (EHS) which is characterized by an elevated internal body temperature above 40°C accompanied by dysfunction or disturbance of the central nervous system.

As part of the return to duty process, the Australian Defence Force recommends that all Australian Defence Force members who have experienced exertional heat stroke are sent for a heat tolerance test. The heat tolerance test is a standard procedure that is performed for all cases of heat stroke to determine their heat tolerance status.

Study participants will be grouped into cases and an unexposed (control) group.

The exposed group (cases) will be female Defence Force members who have been referred to the chief investigator for heat tolerance testing as part of the routine procedure following a heat stroke event.

The unexposed group will be female participants recruited from the general community who have no history of heat illness.

Using the standard heat tolerance test the heat tolerance responses of both the cases and controls will be observed to identify their heat tolerance status (heat tolerant or intolerant). The standard heat tolerance test comprises treadmill walking for 2 hours at 5 km/h and a 2% grade in a climate control chamber set to hot/dry conditions (40°C, 40% relative humidity). The key outcome variables that will be assessed during the 2 hour test will include core temperature, heart rate, skin temperature, sweat rate, and subjective ratings of thermal sensation and thermal comfort. The HTT involves a total of 3.5-4 hours observation.

All participants will also undertake a VO2max test to assess aerobic fitness. Assessment of aerobic fitness will enable us to establish whether the control group is a suitable comparator for the cases as aerobic fitness is known to affect heat tolerance. VO2 will be measured using a metabolic cart and either treadmill or cycle ergometer. The participants will commence the max test at a low intensity to warm up. The exercise intensity will then be progressively increased until the participants reach a point of voluntary exhaustion. This test usually involves 8-15 minutes of exercise and a total of 30-45 mins of total time. The VO2max test can occur within a 4 week period of the heat tolerance test, either beforehand or afterwards.

Alternative heat tolerance test protocol
The current HTT will be considered inappropriate for females if a large proportion of the controls are categorized as heat intolerant (false positive). If the protocol is appropriate, most if not all the control participants should pass the HTT. However, previous studies have shown that a higher proportion of women were classified as heat intolerant using the HTT compared to men.
If the protocol is not valid for females, then the participants will be asked to attend the laboratory on a second occasion to repeat the test with a lower workload. A modified protocol will then be developed.
Intervention code [1] 313503 0
Diagnosis / Prognosis
Comparator / control treatment
The comparator group will include females with no history of heat illness. They will undertake the same standard heat tolerance test protocol as the cases. The criteria used to determine heat intolerance are (a) Tc exceeding 38.6°C, or (b) HR exceeding 160 beats/min, (c) failure of Tc or HR to stabilise during the test or (d) failure to complete the 120 min walk. Heat tolerance responses will be compared between the cases and controls.
Control group
Active

Outcomes
Primary outcome [1] 318870 0
Heat tolerance status (either heat tolerant or heat intolerant) assessed using the standard heat tolerance test.
Timepoint [1] 318870 0
Immediately after completing the standard heat tolerance test.
Secondary outcome [1] 366293 0
Aeobic fitness (is a composite outcome that includes VO2 max, heart rate and subjective rating)

VO2 max test will be conducted using a metabolic cart and either a cycle ergometer (ramp protocol) or treadmill (step protocol commencing at light jogging speed). A mouthpiece for the metabolic cart will be placed in the subject’s mouth and held in place by adjusting the headpiece. A nose clip will be placed on the nose to ensure mouth breathing only. This ensures that all oxygen consumed, and carbon dioxide produced will be measured by the metabolic cart. Heart rate and subjective ratings of effort will be obtained during the test along with the VO2max (maximum oxygen consumed). Heart rate and subjective ratings are used to verify that VO2max is reached during the test.
Timepoint [1] 366293 0
The aerobic fitness will be assessed once within 4 weeks of the heat tolerance test.

Eligibility
Key inclusion criteria
Cases will include female Australian Defence Force members referred to the primary investigator for heat tolerance testing following a known or suspected case of heat stroke or who have previously been referred by their physician for heat tolerance testing. Controls will be female volunteers (civilians) from the general community who have never had a history of heat illness.
Minimum age
18 Years
Maximum age
50 Years
Sex
Females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Potential participants who have any of the following criteria will be excluded from the study:
- Male
- Pregnant or lactating women in the Defence Force or in the general community
- Medical conditions that predisposes and increases the risk of heat stroke
- History of hypertension, malignant hyperthermia, and diabetes
- Currently being treated for any mental disorder which affects their ability to comprehend the study details and therefore their ability to provide consent
- Currently being treated for anaemia
- Currently using glucose lowering agents, prednisone, or beta blockers

Study design
Purpose
Natural history
Duration
Cross-sectional
Selection
Case control
Timing
Prospective
Statistical methods / analysis
A priori power analysis was computed using G-power to determine the sample size. The power analysis indicated that a total of 34 (17 cases and 17 controls) participants are needed to have 80% power for detecting a medium sized effect with a statistical significance criterion level of 0.05. However, the number of control participants will be increased to approximately 30 to increase the power of the study.

Alternative heat tolerance test protocol
The current HTT will be considered inappropriate for females if 10% of the controls are categorized as heat intolerant. If this is the case, the test parameters (treadmill speed and/or grade) will be modified to develop a more appropriate protocol for females.

The statistical analysis will be conducted using SPSS (version 24) and SAS Inst., Cary, NC statistical software. The level of significance will be set at 0.05. The analysis will include comparing the test outcomes for the cases and the controls. An independent sample T test or Man-Whitney U test (based on the normality of the data) will be used to compare the mean/median difference in heart rate and core temperature of the cases and controls. In addition, mathematical modelling to analyse the patterns of the rise in core temperature will be conducted.

Recruitment
Recruitment status
Recruiting
Date of first participant enrolment
Anticipated
3/12/2019
Actual
3/12/2019
Date of last participant enrolment
Anticipated
30/11/2024
Actual
Date of last data collection
Anticipated
30/11/2024
Actual
Sample size
Target
47
Accrual to date
17
Final
Recruitment in Australia
Recruitment state(s)
QLD

Funding & Sponsors
Funding source category [1] 301809 0
Other
Name [1] 301809 0
Researcher consultancy funds
Country [1] 301809 0
Australia
Primary sponsor type
University
Name
James Cook University
Address
1, James Cook Drive, Douglas QLD 4814
Country
Australia
Secondary sponsor category [1] 301552 0
None
Name [1] 301552 0
Address [1] 301552 0
Country [1] 301552 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 302515 0
Departments of Defence and Veterans' Affairs Human Research Ethics Committee (DDVA HREC)
Ethics committee address [1] 302515 0
Ethics committee country [1] 302515 0
Australia
Date submitted for ethics approval [1] 302515 0
20/08/2018
Approval date [1] 302515 0
21/01/2019
Ethics approval number [1] 302515 0
074-18

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 90482 0
Dr Melissa Crowe
Address 90482 0
Division of Tropical Health and Medicine, James Cook University, 1, James Cook Drive, Douglas QLD 4814
Country 90482 0
Australia
Phone 90482 0
+61 7 478 15610
Fax 90482 0
Email 90482 0
[email protected]
Contact person for public queries
Name 90483 0
Melissa Crowe
Address 90483 0
Division of Tropical Health and Medicine, James Cook University, 1, James Cook Drive, Douglas QLD 4814
Country 90483 0
Australia
Phone 90483 0
+61 7 478 15610
Fax 90483 0
Email 90483 0
[email protected]
Contact person for scientific queries
Name 90484 0
Melissa Crowe
Address 90484 0
Division of Tropical Health and Medicine, James Cook University, 1, James Cook Drive, Douglas QLD 4814
Country 90484 0
Australia
Phone 90484 0
+61 7 478 15610
Fax 90484 0
Email 90484 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?




Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.