- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03359928
Acute Physiological and Perceptual Responses to Novel Forms of High-intensity Interval Exercise
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Middlesbrough, United Kingdom
- Teesside University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 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.
Exclusion Criteria:
- 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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: RANDOMIZED
- Interventional Model: CROSSOVER
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Boxing
In 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.
|
as already discussed
|
EXPERIMENTAL: Stair stepping
Participants 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.
|
as already discussed
|
EXPERIMENTAL: Stair climbing
In 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. |
as already discussed
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Heart rate
Time Frame: 6 months
|
Second-to-second heart rate monitoring throughout exercise sessions using wrist worn Polar A360 heart rate monitors
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Mood
Time Frame: 6 months
|
Acute mood state
|
6 months
|
Enjoyment
Time Frame: 6 months
|
Physical activity enjoyment scale (PACES).
Range of possible scores from 18-126, higher scores indicate higher enjoyment.
|
6 months
|
RPE
Time Frame: 6 months
|
Rating of perceived exertion
|
6 months
|
Blood pressure
Time Frame: 6 months
|
Measured using automatic blood pressure monitor
|
6 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Kathryn Weston, PhD, Teesside University
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 162/17
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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