Exercise Performance Clinical Trial
— HITOPOfficial title:
Effects of High-Intensity Interval Training (HIT) While in a Hyperoxic-Hyperbaric Environment on Exercise Performance (HITOP Study)
NCT number | NCT02941939 |
Other study ID # | 1050188 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | April 14, 2016 |
Est. completion date | June 8, 2017 |
Verified date | May 2018 |
Source | Intermountain Health Care, Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Hyperbaric oxygen has previously been tested as a possible means for pre-conditioning to enhance exercise performance. This study is designed to examine the effects of exercising in a hyperbaric chamber for improving fitness when combined with high-intensity training.
Status | Completed |
Enrollment | 50 |
Est. completion date | June 8, 2017 |
Est. primary completion date | April 8, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 40 Years |
Eligibility |
Inclusion Criteria: - Healthy individuals, ages 18-40 years that are sedentary or recreationally active but not involved in any structured endurance training will be eligible for the study. This level of activity will be defined as performing mild-moderate aerobic exercise 0-3 times per week. - VO2 max within normal limits (defined as 84-120% predicted using Wasserman reference equations48). - Spirometry within predicted limits. Exclusion Criteria: - Subjects unable to complete a satisfactory VO2 max test - Individuals with chronic cardiovascular disease such as hypertension, valve disease, coronary artery disease, cardiac conduction abnormalities, etc. - History of pneumothorax or chronic lung disease such as asthma, COPD, bronchiectasis - Active Smokers - Pregnant women - Persons unable to read or understand English, not in full mental capacity or suffer from blindness. |
Country | Name | City | State |
---|---|---|---|
United States | Intermountain Medical Center | Murray | Utah |
Lead Sponsor | Collaborator |
---|---|
Intermountain Health Care, Inc. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in maximum VO2 at 2 weeks compared to baseline | Comparison of post-training VO2 results with baseline in the two HIT groups (performed at ambient conditions in Salt Lake City, UT and hyperbarichyperoxic conditions); the results of HIT at Salt Lake City, UT altitude will be compared with those performed at sea-level altitude in Durham, NC. | 2 weeks | |
Secondary | Change in VO2 measured at anaerobic threshold (in mL O2/kg/min) at 2 weeks compared to baseline | Difference post-training minus pre-training | 2 weeks | |
Secondary | ?VO2/?WR (in mL O2/kg/min/Watt; a measure of exercise efficiency) | Difference post-training minus pre-training | 2 weeks | |
Secondary | Change in peak work rate (in Watts) at 2 weeks compared to baseline | Difference post-training minus pre-training | 2 weeks | |
Secondary | Change in heart rate response to exercise at 2 weeks compared with baseline | Difference post-training minus pre-training | 2 weeks | |
Secondary | Change in level of perceived exertion at 2 weeks compared with baseline | Difference post-training minus pre-training | 2 weeks | |
Secondary | Change in Borg dyspnea score at 2 weeks compared with baseline | Difference post-training minus pre-training | 2 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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