Acute Physiological and Perceptual Responses to Novel Forms of High-intensity Interval Exercise
1 other identifier
interventional
15
1 country
1
Brief Summary
Randomised cross-over study seeking to explore the acute physiological and perceptual responses to three novel forms of high-intensity interval training (HIT).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Nov 2017
Shorter than P25 for not_applicable
1 active site
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
First Submitted
Initial submission to the registry
November 16, 2017
CompletedStudy Start
First participant enrolled
November 20, 2017
CompletedFirst Posted
Study publicly available on registry
December 2, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2018
CompletedSeptember 11, 2018
September 1, 2018
5 months
November 16, 2017
September 10, 2018
Conditions
Outcome Measures
Primary Outcomes (1)
Heart rate
Second-to-second heart rate monitoring throughout exercise sessions using wrist worn Polar A360 heart rate monitors
6 months
Secondary Outcomes (4)
Mood
6 months
Enjoyment
6 months
RPE
6 months
Blood pressure
6 months
Study Arms (3)
Boxing
EXPERIMENTALIn each of the three sessions a different exercise modality will be conducted, in a randomised sequence. Non-contact boxing involves boxing "punch pads" that will be held by the one of the researchers, while wearing protective boxing gloves. Each exercise modality will be conducted following a high-intensity interval protocol (4 x 60 seconds of exercise interspersed with 60 seconds of rest). During each exercise bout participants will be encouraged to exercise at an intensity that elicits a heart rate of ≥85% of maximum, which will always be followed by 60 seconds of passive recovery. Participants will complete a 5 minute warm-up and a 2 minute cool down and stretch after the exercise bouts have been completed.
Stair stepping
EXPERIMENTALParticipants will complete 3 sessions of exercise. In each of the three sessions a different exercise modality will be conducted in a randomised sequence. Stair stepping involves stepping on to and off a 35 cm Reebok exercise bench, repeatedly. Each exercise modality will be conducted following a high-intensity interval protocol (4 x 60 seconds of exercise interspersed with 60 seconds of rest). During each exercise bout participants will be encouraged to exercise at an intensity that elicits a heart rate of ≥85% of maximum, which will always be followed by 60 seconds of passive recovery. Participants will complete a 5 minute warm-up and a 2 minute cool down and stretch after the exercise bouts have been completed.
Stair climbing
EXPERIMENTALIn each of the three sessions a different exercise modality will be conducted, in a randomised sequence. Stair climbing involves continuously ascending the stairs located in a public access staircase. Each exercise modality will be conducted following a high-intensity interval protocol (4 x 60 seconds of exercise interspersed with 60 seconds of rest). During each exercise bout participants will be encouraged to exercise at an intensity that elicits a heart rate of ≥85% of maximum, which will always be followed by 60 seconds of passive recovery. Participants will complete a 5 minute warm-up and a 2 minute cool down and stretch after the exercise bouts have been completed.
Interventions
Eligibility Criteria
You may qualify if:
- adult (≥18 years) employees
- no health conditions that preclude them from exercise and on no medication, information obtained via their self-report.
- able to understand written and spoken English.
- participants reporting that they are asthmatic will allowed to participate with medical clearance and instructed to bring their bronchodilator medication and use it when required.
You may not qualify if:
- symptoms of or known presence of heart disease
- condition or injury or co-morbidity affecting the ability to undertake exercise
- diabetes mellitus
- early family history of sudden cardiac death
- pregnancy or likelihood of pregnancy.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Teesside University
Middlesbrough, United Kingdom
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Kathryn Weston, PhD
Teesside University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
November 16, 2017
First Posted
December 2, 2017
Study Start
November 20, 2017
Primary Completion
April 30, 2018
Study Completion
April 30, 2018
Last Updated
September 11, 2018
Record last verified: 2018-09
Data Sharing
- IPD Sharing
- Will not share