- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05573087
Comparing Land-based and Aquatic Reduced Exertion High Intensity Interval Training in Sedentary Young Adults
October 5, 2022 updated by: Miriam Leary, West Virginia University
Previous research has found improvements in performance (VO2max) and clinical (insulin resistance) with cycling REHIIT.
In some populations (e.g.
obese, arthritic) aquatic exercise is a safer, more enjoyable option.
However, to date, no study has yet examined whether aquatic REHIIT confers the same benefits as land-based REHIIT.
Therefore, the purpose of this study is to determine whether there are significant differences in clinical and performance outcomes between a land-based and comparable aquatics based Reduced Exertion High Intensity Interval Training (REHIIT) protocol.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
32
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
West Virginia
-
Morgantown, West Virginia, United States, 26506
- West Virginia University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 30 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- English speaking
- sedentary individuals; Sedentary will be defined as less than 150 minutes of exercise/week as defined by the CDC and American College of Sports Medicine
- All subjects will be screened with a resting 12 lead EKG to ensure they are safe to exercise
Exclusion Criteria:
- Any vulnerable populations will be excluded including adults unable to consent/Cognitively Impaired
- individuals who are not yet adults
- pregnant or nursing women
- prisoners or other detained individuals
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
ACTIVE_COMPARATOR: Aquatic Based Exercise
maximal jump squats in a pool
|
10 minutes of exercise with two 20 second sprints three days per week for 8 consecutive weeks
|
|
ACTIVE_COMPARATOR: Land Based Exercise
cycle ergometer
|
10 minutes of exercise with two 20 second sprints three days per week for 8 consecutive weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in Cardiorespiratory Fitness
Time Frame: Baseline to 8 weeks
|
Percent changes in VO2 is milliliters of oxygen per kilogram of body weight per minute (oxygen in milliliters, weight in kilograms, and time in minutes and expressed in ml/kg/min).
|
Baseline to 8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Miriam Leary, PhD, West Virginia University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
January 19, 2021
Primary Completion (ACTUAL)
December 31, 2021
Study Completion (ACTUAL)
December 31, 2021
Study Registration Dates
First Submitted
October 5, 2022
First Submitted That Met QC Criteria
October 5, 2022
First Posted (ACTUAL)
October 10, 2022
Study Record Updates
Last Update Posted (ACTUAL)
October 10, 2022
Last Update Submitted That Met QC Criteria
October 5, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 1911776700
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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