NCT07198334

Brief Summary

This study is the first to examine the effects of short passive heat exposure on heat acclimation (HA). Unlike traditional protocols requiring prolonged heat exposure, this study tests whether a daily 5-minute whole-body immersions at 45°C water repeated over two weeks can trigger adaptive responses, offering a potentially more accessible and time-efficient method for heat acclimation. This study aims to investigate whether brief, repeated passive heat exposure can induce HA in both female and male participants. It evaluates changes across physiological, biological, and psychological markers to determine the efficacy of this minimal-exposure protocol. It is hypothesized that such short, repeated immersions may be sufficient to elicit significant adaptive responses across key HA indicators.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
26

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Oct 2020

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2020

Completed
3.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 31, 2024

Completed
1.3 years until next milestone

First Submitted

Initial submission to the registry

September 25, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

September 30, 2025

Completed
Last Updated

December 24, 2025

Status Verified

December 1, 2025

Enrollment Period

3.7 years

First QC Date

September 25, 2025

Last Update Submit

December 17, 2025

Conditions

Outcome Measures

Primary Outcomes (17)

  • Dehydration (kg)

    Dehydration (in kg) was assessed by calculating body mass loss (Tanita Body Composition Analyzer; USA) during heat exposure.

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Heart rate (bpm)

    Heart rate (in bpm) was recorded using a heart rate sensor with a chest strap (Polar, Finland).

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Blood pressure (mmHg)

    Systolic and diastolic blood pressure (in mmHg) was measured using with an automatic cuff monitor (Gentle+, Microlife, Switzerland).

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Pulse pressure (mmHg)

    Pulse pressure (in mmHg) was calculated by subtracting diastolic blood pressure from systolic blood pressure.

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Rate of pressure production (AU)

    Rate of pressure production (in AU) was calculated by multiplying heart rate , by systolic blood pressure.

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Shivering/sweating (points)

    The shivering/sweating rate will be evaluated using 7-point scale. The rating of shivering/sweating range from 1 (heavily sweating) to 7 (vigorously shivering), with 4 being neutral.

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Thermal comfort (points)

    Thermal comfort will be evaluated using 4-point scale. The rating of thermal comfort range from 0 (neutral) to 3 (very uncomfortable).

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Body temperature (°C)

    Rectal temperature (in °C) was measured using a thermocouple (Rectal Probe, Ellab, Denmark) inserted to a depth of 12 cm past the anal sphincter, skin temperature (in °C) was measured with thermistors (Skin/Surface Probe, DM852, Ellab), and muscle temperature (in °C) was measured using a needle microprobe (MKA; Ellab).

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Physiological strain index

    Physiological strain index (PSI) was used to indicate heat strain. PSI = 5 x (Tret - Tre0) x (39.5 - Tre0)\^-1+ 5 x (HRt - HR0) x (180 - HR0)\^-1, where rectal temperature (Tre) t and heart rate (HR) t are simultaneous measurements taken at the end of the heat exposure and Tre0 and HR0 are the initial measurements.

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Oxygen consumption (mL/min/kg)

    Oxygen consumption (in mL/min/kg) was measured using Cortex METALYZR® 3B, Leipcig, Germany).

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Carbon dioxide output (mL/min/kg)

    Carbon dioxide output (in mL/min/kg) was measured using Cortex METALYZR® 3B, Leipcig, Germany).

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Carbon dioxide output (mL/min)

    Carbon dioxide output (in mL/min) was measured using Cortex METALYZR® 3B, Leipcig, Germany).

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Oxygen consumption (mL/min)

    Oxygen consumption (in mL/min) was measured using Cortex METALYZR® 3B, Leipcig, Germany).

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Respiratory quotient

    The respiratory quotient was calculated by dividing the carbon dioxide output by the oxygen consumption. This ratio was used to assess substrate utilization. The values for fat is assumed as 0.7, for protein is assumed as 0.8 and for carbohydrate is assumed as 1.0.

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Ventilation (L/min)

    Ventilation (in L/min) was measured using Cortex METALYZR® 3B, Germany).

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Tidal volume (L)

    Tidal volume (in L) was measured using Cortex METALYZR® 3B, Germany).

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Breathing frequency (t/min)

    Breathing frequency (t/min) was measured using Cortex METALYZR® 3B, Germany).

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

Secondary Outcomes (8)

  • Height (cm)

    During enrollment

  • Body mass and body composition (kg)

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Body mass index (kg/m^2)

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Body composition (%)

    From enrollment to the end of deacclimation (one month after the 14-day heat acclimation period).

  • Maximal oxygen consumption (in mL/min/kg)

    During enrollment

  • +3 more secondary outcomes

Study Arms (1)

Heat acclimation

EXPERIMENTAL
Other: Heat acclimation

Interventions

Passive heat acclimation was designed to induce adaptation in participants through 14 consecutive days of controlled 5-minute whole-body immersion in water at 45°C.

Heat acclimation

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Healthy, non-obese males and females aged 18 to 35 years with a body mass index between 18.5 and 29.9 kg/m².
  • No participation in temperature manipulation programs (e.g., cold or heat acclimation) within the past three months.
  • No engagement in excessive formal exercise.
  • Female participants must have a regular menstrual cycle.

You may not qualify if:

  • Current smokers.
  • Fear of needles or blood.
  • Use of medications or supplements that could affect study outcomes.
  • History of neurological, cardiovascular, metabolic, or inflammatory diseases that could be aggravated by hot water exposure.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Lithuanian Sports University

Kaunas, Lithuania

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 25, 2025

First Posted

September 30, 2025

Study Start

October 1, 2020

Primary Completion

May 31, 2024

Study Completion

May 31, 2024

Last Updated

December 24, 2025

Record last verified: 2025-12

Locations