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Trial registered on ANZCTR
Registration number
ACTRN12623001302640
Ethics application status
Approved
Date submitted
22/11/2023
Date registered
14/12/2023
Date last updated
14/12/2023
Date data sharing statement initially provided
14/12/2023
Type of registration
Prospectively registered
Titles & IDs
Public title
Blood pressure response to differing modes of hot-water immersion
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Scientific title
Blood pressure response to differing modes of hot-water immersion in healthy adults
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Secondary ID [1]
311009
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None
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Hypertension
332119
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Condition category
Condition code
Cardiovascular
328848
328848
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0
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Hypertension
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
All participants will complete 3 water immersion sessions and a control session (in a randomised order): 1) 30-min whole-body hot-water immersion (40°C; chest depth), 2) 30-min waist deep hot-water immersion (40°C), 3) 30-min lower-limb hot-water immersion (~40°C; below knee depth).
There will be a 4-day washout between exposures.
1. 30-min whole-body hot-water immersion (40°C)
Location: School of Physical Education, Sport and Exercise Sciences Aquatic Facility (University of Otago, Dunedin).
Supervision: This session will be supervised by an American College of Sports Medicine (ACSM) registered clinical exercise physiologist (CEP), and the primary investigator (PI) or a research assistant; all supervising researchers are first aid trained. Attendance and session particulars (e.g., physiological indices etc.) will be recorded at each session by the supervising researcher.
Exposure: Participants will complete a single 30-min hot water immersion session in 40 °C water. Participants will be seated upright with water approximately nipple level.
Duration: 30 min.
2. 30-min waist-deep hot-water immersion (40°C)
Location: School of Physical Education, Sport and Exercise Sciences Aquatic Facility (University of Otago, Dunedin).
Supervision: This session will be supervised by an American College of Sports Medicine (ACSM) registered clinical exercise physiologist (CEP), and the PI or a research assistant; all supervising researchers are first aid trained. Attendance and session particulars (e.g., physiological indices etc.) will be recorded at each session by the supervising researcher.
Exposure: Participants will complete a single 30-min hot water immersion session in 40 °C water. Participants will be seated upright with water approximately waist deep level.
Duration: 30 min.
3. 30-min lower-limb hot-water immersion (40°C)
Location: School of Physical Education, Sport and Exercise Sciences Aquatic Facility (University of Otago, Dunedin).
Supervision: This session will be supervised by an American College of Sports Medicine (ACSM) registered clinical exercise physiologist (CEP), and the PI or a research assistant; all supervising researchers are first aid trained. Attendance and session particulars (e.g., physiological indices etc.) will be recorded at each session by the supervising researcher.
Exposure: Participants will complete a single 30-min hot water immersion session in 40 °C water. Participants will be seated upright with water approximately at below knee level.
Duration: 30 min.
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Intervention code [1]
327448
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Treatment: Other
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Comparator / control treatment
30-min control (no exposure).
Location: School of Physical Education, Sport and Exercise Sciences Aquatic Facility (University of Otago, Dunedin).
Supervision: This session will be supervised by an American College of Sports Medicine (ACSM) registered clinical exercise physiologist (CEP), and the PI or a research assistant; all supervising researchers are first aid trained. Attendance and session particulars (e.g., physiological indices etc.) will be recorded at each session by the supervising researcher.
Exposure: Participants will complete a single 30-min resting session (i.e., no exposure/water immersion). Participants will be seated upright in a chair.
Duration: 30 min.
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Control group
Active
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Outcomes
Primary outcome [1]
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Blood pressure
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Assessment method [1]
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Assessed via ausculatory method (using sphygmomanometer and) stethoscope and ambulatory method (using 24 hour blood pressure monitor)
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Timepoint [1]
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Pre-exposure, during exposure (every 10 mins), immediately post-completion of exposure and every hour across 24-h post-completion of exposure.
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Secondary outcome [1]
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Physical activity
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Assessment method [1]
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Assessed via accelerometry
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Timepoint [1]
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Across the 24-h post-completion of exposure
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Secondary outcome [2]
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Heart rate
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Assessment method [2]
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Assessed via chest strap
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Timepoint [2]
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Pre-exposure, during exposure (e.g., every 10 mins) and immediately post-completion of exposure.
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Secondary outcome [3]
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Core temperature
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Assessment method [3]
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Assessed via rectal thermistor
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Timepoint [3]
429150
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Pre-exposure, during exposure (every 10mins) and immediately post-completion of exposure
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Eligibility
Key inclusion criteria
- 18-65 years old;
- Either sex or any gender;
- Any ethnicity;
- Healthy;
- Patient gives written consent;
- Patient is able to travel to the study centre to complete all sessions.
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Minimum age
18
Years
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Maximum age
65
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
- Be hypertensive when at seated rest (Stage 2: systolic or diastolic blood pressure >130 mm Hg or >90 mm Hg, respectively);
- A “yes” response to the follow-up questions on the Physical Activity Readiness Questionnaire
- Contraindication to maximal exercise testing;
- Angina;
- Recent myocardial infarction (< 3 months ago);
- Implanted cardiac device (i.e. ICD, pacemaker etc.);
- Heat intolerance;
- Pregnancy;
- History of large blood pressure decreases or fainting;
- Any other medical condition deemed a significant risk to study participation.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Allocation will not be concealed
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation using a randomisation table created by computer software (i.e. computerised sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
18/12/2023
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
10
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
25981
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New Zealand
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State/province [1]
25981
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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University of Otago
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Address [1]
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Update Heart Otago Department of Physiology School of Biomedical Sciences University of Otago PO Box 56 Dunedin 9054 New Zealand
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Country [1]
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New Zealand
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Primary sponsor type
University
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Name
University of Otago
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Address
362 Leith Street Dunedin North Dunedin 9016
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Country
New Zealand
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
317308
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Country [1]
317308
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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University of Otago Human Ethics Committee - Health
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Ethics committee address [1]
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362 Leith Street Dunedin North Dunedin 9016
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Ethics committee country [1]
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New Zealand
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Date submitted for ethics approval [1]
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06/11/2023
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Approval date [1]
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20/11/2023
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Ethics approval number [1]
314192
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Summary
Brief summary
This 4x4 randomised crossover study will aim to recruit 10 healthy participants. Participants will complete 4 sessions: 1) 30-min whole-body (chest deep) hot-water immersion (40°C), 2) 30-min waist deep hot-water immersion (40°C), 3) 30-min lower-limb (knee deep in 40°C), and 4) 30-min control (no exposure). The order for the four exposures will be randomised using a 4x4 Latin square design. Physiological measures will be taken during each exposure to characterise the stimulus (e.g., beat-to-beat blood pressure, heart rate, core temperature). Following each exposure participants will be fitted with an ambulatory blood pressure monitor (and accelerometer to confirm standardisation of activity levels) for the following 24 h to quantify the magnitude and duration of post-session hypotension.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr Brendon Roxburgh
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Address
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Department of Surgical Sciences Level 4, Dunedin Public Hospital 201 Great King Street, Central Dunedin, Dunedin 9016
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Country
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New Zealand
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Phone
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+64 274632376
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Brendon Roxburgh
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Address
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Department of Surgical Sciences Level 4, Dunedin Public Hospital 201 Great King Street, Central Dunedin, Dunedin 9016
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Country
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New Zealand
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Phone
130739
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+64 274632376
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Fax
130739
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Email
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[email protected]
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Contact person for scientific queries
Name
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Brendon Roxburgh
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Address
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Department of Surgical Sciences Level 4, Dunedin Public Hospital 201 Great King Street, Central Dunedin, Dunedin 9016
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Country
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New Zealand
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Phone
130740
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+64 274632376
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Fax
130740
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Email
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
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.
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