Work Rate Adjustments During a High-intensity Interval Training on a Stationary Bike in a Hot and Temperate Environment

Sponsor
University of Alabama, Tuscaloosa (Other)
Overall Status
Completed
CT.gov ID
NCT05988606
Collaborator
(none)
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Study Details

Study Description

Brief Summary

The goal of this repeated measures study is to evaluate acute work rate adjustments during high-intensity interval training (HIIT) in a hot and temperate environment in healthy and active adults when using target heart rate to prescribe the exercise intensity.

The main questions it aims to answer are:
  • Will HIIT based on target heart rate in a hot environment result in increased cardiovascular (i.e., elevated recovery HR) and thermal strain compared to HIIT in a temperate environment?

  • Will work rate be lowered to a greater extent during HIIT in a hot environment compared to a temperate environment in order to maintain target heart rate?

  • Will maximal aerobic capacity (V̇O2max) decrease to a greater extent after HIIT in the heat compared to a temperate environment?

Procedures:
Participants will complete 5 trials on a cycle ergometer. Trial 1 (Control Visit):

Participants (n = 7) will have their maximal heart rate and V̇O2max measured in a temperate environment (~22 °C, 40% RH).

Experimental Trials 2-5: The order of the trials will be counterbalanced and randomly assigned to participants.

  • 15TEMP: Participants will cycle at 70% of their maximum heart rate for 8 minutes as a warm-up, followed by one round of HIIT. The HIIT protocol consists of 4 minutes at 90% of maximum heart rate followed by 3 minutes at 70% of maximum heart rate, totaling 15 minutes, in a temperate environment (~22 °C, 40% RH). After the HIIT session, a graded exercise test will measure V̇O2max.

  • 15HEAT: Similar to 15TEMP, but participants will perform the HIIT protocol in a hot environment (~35 °C, 40% RH).

  • 43TEMP: Participants will cycle at 70% of their maximum heart rate for 8 minutes as a warm-up, followed by the HIIT protocol repeated four times (4 minutes at 90% of maximum heart rate and 3 minutes at 70% of maximum heart rate), totaling 43 minutes, in a temperate environment (~22 °C, 40% RH).

  • 43HEAT: Similar to 43TEMP, but participants will perform the HIIT protocol in a hot environment (~35 °C, 40% RH).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: 15 minutes of high-intensity interval training
  • Behavioral: 43 minutes of high-intensity interval training
  • Other: Hot environment
  • Other: Temperate environment
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
7 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
Participants completed all trials and were compared to themselves.Participants completed all trials and were compared to themselves.
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Acute Work Rate Adjustments During High-intensity Interval Training in a Hot and Temperate Environment
Actual Study Start Date :
May 12, 2021
Actual Primary Completion Date :
Nov 14, 2021
Actual Study Completion Date :
Nov 14, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: 15TEMP

Participants cycled at 70% heart rate max for 8 min as a warm-up and then completed one round of HIIT, i.e., 4 min at 90% heart rate max followed by 3 min at 70% heart rate max for a total of 15 minutes in a temperate environment, followed by a graded exercise test to measure maximal aerobic capacity.

Behavioral: 15 minutes of high-intensity interval training
Participants completed an 8 min warm-up and 1 round of high-intensity interval training

Other: Temperate environment
Participants exercised in a temperate environment, ~ 22 °C, ~40% relative humidity.

Experimental: 15HEAT

Participants cycled at 70% heart rate max for 8 min as a warm-up and then completed one round of HIIT, i.e., 4 min at 90% heart rate max followed by 3 min at 70% heart rate max for a total of 15 minutes in a hot environment, followed by a graded exercise test to measure maximal aerobic capacity.

Behavioral: 15 minutes of high-intensity interval training
Participants completed an 8 min warm-up and 1 round of high-intensity interval training

Other: Hot environment
Participants exercised in a hot environment, ~ 35 °C, ~40% relative humidity.

Experimental: 43TEMP

Participants cycled at 70% heart rate max for 8 min as a warm-up and then performed the HIIT protocol (4 min at 90% heart rate max and 3 min at 70% heart rate max, repeated 4 times for a total of 43 minutes) in a temperate environment followed by a graded exercise test to measure maximal aerobic capacity.

Behavioral: 43 minutes of high-intensity interval training
Participants completed an 8 min warm-up and 5 rounds of high-intensity interval training

Other: Temperate environment
Participants exercised in a temperate environment, ~ 22 °C, ~40% relative humidity.

Experimental: 43HEAT

Participants cycled at 70% heart rate max for 8 min as a warm-up and then performed the HIIT protocol (4 min at 90% heart rate max and 3 min at 70% heart rate max, repeated 4 times for a total of 43 minutes) in a hot environment followed by a graded exercise test to measure maximal aerobic capacity.

Behavioral: 43 minutes of high-intensity interval training
Participants completed an 8 min warm-up and 5 rounds of high-intensity interval training

Other: Hot environment
Participants exercised in a hot environment, ~ 35 °C, ~40% relative humidity.

No Intervention: Control

Participants completed a graded exercise test on a stationary bicycle in a temperate environment (~ 22 °C (72 °F), ~40% RH) to measure maximal aerobic capacity and maximal heart rate.

Outcome Measures

Primary Outcome Measures

  1. Work rate adjustments [From the first work interval (min 9-12) to the last work interval (min 37-40).]

    In a hot and temperate environment by how much does work rate need to be adjusted to maintain target heart rate?

Secondary Outcome Measures

  1. Cardiovascular strain [From the first recovery interval (min 13-15) to the last recovery interval (min 41-43).]

    In a hot and temperate environment by how much does heart rate in the recovery intervals increase?

  2. Thermal Strain [From the first work interval (min 9-12) to the last work interval (min 37-40).]

    In a hot and temperate environment by how much do rectal temperature and skin temperature increase?

  3. Maximal aerobic capacity [The end of the 15 min trials compared to the end of the 43 min trials.]

    In a hot and temperate environment by how much does maximal aerobic capacity decrease?

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 39 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Participants were healthy males and females who are 18 to 39 years of age, recreationally active as defined by the American College of Sports Medicine, performing moderate-intensity aerobic exercise 30 min or more per session for at least 3 sessions per week for at least the past 3 months, and free of metabolic, cardiovascular, and renal disease
Exclusion Criteria:
  • Individuals classified as needing medical clearance according to American College of Sports Medicine (ACSM) Guidelines were not allowed to participate. Needing medical clearance is defined by ACSM as 1) not being physically active and having known cardiovascular, metabolic, or renal disease and asymptomatic; 2) not being physically active and having any signs or symptoms suggestive of cardiovascular, metabolic, or renal disease; 3) participating in regular exercise and having known cardiovascular, metabolic, or renal disease and asymptomatic; or 4) participating in regular exercise and having any signs or symptoms suggestive of cardiovascular, metabolic, or renal disease .

Contacts and Locations

Locations

Site City State Country Postal Code
1 The University of Alabama Tuscaloosa Alabama United States 35487

Sponsors and Collaborators

  • University of Alabama, Tuscaloosa

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Alabama, Tuscaloosa
ClinicalTrials.gov Identifier:
NCT05988606
Other Study ID Numbers:
  • 21-02-4359
First Posted:
Aug 14, 2023
Last Update Posted:
Aug 14, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 14, 2023