The Effects of Post Aerobic Exercise Hot Water Immersion on Physiological and Perceptual Responses in Physically Inactive Middle-aged Adults

Sponsor
Coventry University (Other)
Overall Status
Completed
CT.gov ID
NCT05035004
Collaborator
(none)
16
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4

Study Details

Study Description

Brief Summary

This study will investigate the effects of post moderate intensity aerobic exercise hot water immersion on physiological and perceptual responses in physically inactive middle-aged adults when compared to moderate intensity aerobic exercise and hot water immersion alone.

Condition or Disease Intervention/Treatment Phase
  • Device: Post exercise hot water immersion
  • Device: Exercise
  • Device: Hot water immersion
N/A

Detailed Description

A large number of middle aged adults do not achieve the minimum recommended amount of physical activity. This consequently increases the risk of cardiovascular disease and all-cause mortality. Although below the recommended physical activity guidelines, it is important to highlight that a considerable proportion of these individuals do take part in some form of physical activity within their weekly routines. Hence, identifying complementary therapies that can enhance the health benefits from smaller amounts of exercise are of great value for many physically inactive middle-aged adults.

An in increase in body temperature from a single session of passive heating has been shown to mimic many of the beneficial physiological responses of exercise, such as, an increase in heart rate, skin blood flow and an increase in circulating angiogenic factors. However, lab based studies often push participants to the limit of thermal tolerance which may reduce long term adherence in the real world. Therefore, this study will investigate whether the use of post exercise hot water immersion can prolong and / or intensify exercise mediated physiological responses that underpin health benefits, whilst also assessing the perceptual responses, in comparison to exercise and hot water immersion alone.

Through the use of a repeated measures design, participants will randomly take part in three conditions; 1) post exercise hot water immersion (30 minutes of moderate intensity cycling followed by 10 minutes of supine rest and 30 minutes of whole body hot water immersion at 40°C); 2) aerobic exercise (30 minutes of moderate intensity cycling followed by 10 minutes of supine rest and 30 minutes of seated rest at room temperature); 3) hot water immersion condition (30 minutes of whole body hot water immersion at 40°C followed by 10 minutes of supine rest and 30 minutes of whole body hot water immersion at 40°C). Each condition will be separated by a minimum of 1-week. Outcome measures will either be assessed at regular intervals or at 0, 30, 70 and 100 minute time points for each condition.

Study Design

Study Type:
Interventional
Actual Enrollment :
16 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
The Effects of Post Aerobic Exercise Hot Water Immersion on Physiological and Perceptual Responses in Physically Inactive Middle-aged Adults
Actual Study Start Date :
Nov 15, 2021
Actual Primary Completion Date :
Mar 16, 2022
Actual Study Completion Date :
Mar 16, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Post exercise hot water immersion

Moderate intensity cycling for 30 minutes, followed by a 10-minute transfer period and then 30 minutes of whole-body hot water immersion.

Device: Post exercise hot water immersion
Participants will complete 30 minutes of cycling on a lode bicycle ergometer (50% of VO2max), followed by a 10-minute transfer period and then 30 minutes of whole-body hot water immersion in a hot tub (water temperature 40°C).

Active Comparator: Exercise

Moderate intensity cycling for 30 minutes.

Device: Exercise
Participants will complete 30 minutes of cycling on a lode bicycle ergometer (50% of VO2max).

Active Comparator: Hot water immersion

Whole-body hot water immersion for 30 minutes, followed by a 10-minute transfer period and then an additional 30 minutes of whole-body hot water immersion.

Device: Hot water immersion
Participants will complete 30 minutes of whole-body hot water immersion in a hot tub (water temperature 40°C), followed by a 10-minute transfer period and then an additional 30 minutes of whole-body hot water immersion in a hot tub (water temperature 40°C).

Outcome Measures

Primary Outcome Measures

  1. Change in circulating plasma nitrite (pg/ml) [Measured at 0, 30, 70 and 100 minutes]

    Venous blood sample

  2. Change in brachial artery total shear rate (S-1) [Measured at 0, 30, 70 and 100 minutes]

    Terason ultrasound recording of the brachial and superficial femoral artery

  3. Change in brachial artery antegrade shear rate (S-1) [Measured at 0, 30, 70 and 100 minutes]

    Terason ultrasound recording of the brachial and superficial femoral artery.

  4. Change in brachial artery retrograde shear rate (S-1) [Measured at 0, 30, 70 and 100 minutes]

    Terason ultrasound recording of the brachial and superficial femoral artery

  5. Change in brachial artery diameter (mm) [Measured at 0, 30, 70 and 100 minutes]

    Terason ultrasound recording of the brachial and superficial femoral artery

  6. Change in brachial artery blood flow (ml/min) [Measured at 0, 30, 70 and 100 minutes]

    Terason ultrasound recording of the brachial and superficial femoral artery.

  7. Change in brachial artery compliance (μm/mmHg) [Measured at 0, 30, 70 and 100 minutes]

    Terason ultrasound recording of the brachial artery. Brachial artery compliance will be calculated by using the change in blood volume and blood pressure

  8. Change in systolic blood pressure (mmHg) [Measurements taken at 10 minute intervals up to 100 minutes]

    Measured using an automated blood pressure cuff

  9. Change in diastolic blood pressure (mmHg) [Measurements taken at 10 minute intervals up to 100 minutes]

    Measured using an automated blood pressure cuff

  10. Change in mean arterial pressure (mmHg) [Measurements taken at 10 minute intervals up to 100 minutes]

    Measured using an automated blood pressure cuff. Mean arterial pressure will be calculated by using systolic and diastolic blood pressure

  11. Change in pulse pressure (mmHg) [Measurements taken at 10 minute intervals up to 100 minutes]

    Measured using an automated blood pressure cuff. Pulse pressure will be calculated using systolic and diastolic blood pressure

Secondary Outcome Measures

  1. Change in circulating serum Interleukin-6 (pg/ml) [Measured at 0, 30, 70 and 100 minutes]

    Venous blood sample

  2. Change in circulating serum Interleukin-10 (pg/ml) [Measured at 0, 30, 70 and 100 minutes]

    Venous blood sample

  3. Change in circulating serum Interleukin-8 (pg/ml) [Measured at 0, 30, 70 and 100 minutes]

    Venous blood sample

  4. Change in circulating serum Interleukin-1Ra (pg/ml) [Measured at 0, 30, 70 and 100 minutes]

    Venous blood sample

  5. Change in circulating serum Vascular endothelial growth factor (pg/ml) [Measured at 0, 30, 70 and 100 minutes]

    Venous blood sample

  6. Change in circulating serum Endothelin-1 (pg/ml) [Measured at 0, 30, 70 and 100 minutes]

    Venous blood sample

  7. Circulating serum Monocyte chemoattractant protein-1 (pg/ml) [Measured at 0, 30, 70 and 100 minutes]

    Venous blood sample

  8. Change in circulating serum Matrix metallopeptidase-2 (pg/ml) [Measured at 0, 30, 70 and 100 minutes]

    Venous blood sample

  9. Change in circulating serum Matrix metallopeptidase-9 (pg/ml) [Measured at 0, 30, 70 and 100 minutes]

    Venous blood sample

  10. Energy expenditure (kcal/h-1) [Gas measurements taken continually up to 70 minutes. Energy expenditure calculated from the 30 minutes of exercise, hot water immersion and/or rest periods.]

    Measured initially by breath by breath analysis through the use of a Ultima and calculated via indirect calorimetry

  11. Change in thermal comfort [Measured at 10 minute intervals up to 100 minutes]

    Thermal comfort Likert scale from a positive score of +5 very comfortable (maximum) to a negative score of -5 very uncomfortable (minimum)

  12. Change in thermal sensation [Measured at 10 minute intervals up to 100 minutes]

    Thermal sensation Likert scale from +5 (maximum) hot to -5 cold (minimum)

  13. Change in basic affect [Measured at 10 minute intervals up to 100 minutes]

    Basic affect Likert scale from a positive score of +5 very good (maximum) to a negative score of -5 very bad (minimum)

  14. Change in physical activity enjoyment scale [Measured ~12 minutes post intervention]

    Feelings about exercise and / or passive heating on a Likert scale from a positive score of 1 (maximum) to a negative score of 7 (minimum)

Other Outcome Measures

  1. Change in rectal core temperature (°C) [Measurements taken at 10 minute intervals up to 100 minutes]

    Measured using a rectal probe attached to a squirrel data logger

  2. Change in forehead skin temperature (°C) [Measurements taken at 10 minute intervals up to 100 minutes]

    Measured using skin thermistors attached to a squirrel data logger

  3. Change in heart rate (bpm) [Measurements taken at 10 minute intervals up to 100 minutes]

    Measured using a heart rate monitor

  4. Change in plasma volume (%) [Measurements taken pre and immediately post intervention]

    Measured by a capillary blood sample then calculating plasma volume via the hemoglobin and hematocrit

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Males and post menopausal females

  • Aged between 40 - 60 years

  • BMI of 18.5 - 34.9 kg/m2

  • Over the last 6 months has participated in less than 150 mins of moderate intensity physical activity or 75 mins of vigorous activity or a combination of both, but takes part in some form of physical activity within their weekly routine.

  • Maximal oxygen uptake categorised as 'fair' for a given age group.

Exclusion Criteria:
  • Previous myocardial infarction or cerebrovascular event

  • Any signs or symptoms of cardiovascular issues

  • High blood pressure: SBP >180 mmHg and / or DBP >100 mmHg

  • Orthostatic hypotension: Drop of SBP > 20mmHg and / or DBP >10 mmHg upon standing.

  • Changed blood pressure medication in the 6-month period prior to the study

  • Plan to change any form of relevant medication during study period

  • Suffers from diabetes

  • Suffers from severe asthma

  • Currently have any infections or symptoms of an infection (e.g. COVID-19 etc)

  • Suffers from a neurodegenerative disease

  • Cannot understand and/or fully cooperate with the study protocol

  • Exercise-limiting comorbidity (e.g. angina, chronic lung disease, arthritis etc)

  • Severe peripheral neuropathy (cannot sense temperature)

  • Current smoker or have stopped in the last 3 months

  • Any skin conditions including ulcerations

  • Exposed to high temperatures in the last 4-weeks (e.g. holiday, spa, sun beds etc)

  • Use of antioxidant supplements in the last 6-weeks

Contacts and Locations

Locations

Site City State Country Postal Code
1 Coventry University Coventry West Midlands United Kingdom CV1 5FB

Sponsors and Collaborators

  • Coventry University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Charles Steward, Post Graduate Research Student in the Centre for Sport, Exercise and Life Sciences, Coventry University
ClinicalTrials.gov Identifier:
NCT05035004
Other Study ID Numbers:
  • P97102
First Posted:
Sep 5, 2021
Last Update Posted:
Mar 17, 2022
Last Verified:
Mar 1, 2022
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 Mar 17, 2022