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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04448925
Other study ID # UTexasAustinHPL
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 10, 2019
Est. completion date June 20, 2020

Study information

Verified date June 2020
Source University of Texas at Austin
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The optimal recovery duration depends on the intensity of exercise and in the present study the intensity was maximal power for 4-s while cycling an 'Inertial Load' ergometer (ILE). Recovery duration of 15, 30 and 45-s were given between 30 successive sprints.


Description:

All subjects completed an informed consent for this study that was approved by the Institutional Review Board of the University of Texas at Austin.

Study Overview. A randomized, cross-over experimental design was conducted. Each participant visited the laboratory on four occasions which were separated by two to five days. Measurement of body mass, familiarization with experimental procedures and cycling peak oxygen consumption test (VO2peak) were performed on the first visit. Participants took part in inertial-load exercise (ILE) on the remaining test days. On each separate session, a different inter-sprint recovery duration was employed (i.e. 15, 30 or 45-s). Cycling power output, pulmonary gas exchange, vastus lateralis de-oxygenation status, heart rate and blood lactate were measured.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date June 20, 2020
Est. primary completion date July 20, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- healthy participants

Exclusion Criteria:

- unhealthy

Study Design


Related Conditions & MeSH terms

  • Exercise, Cardiovascular Function, Fatigue, Muscular Power
  • Fatigue

Intervention

Other:
inertial-load exercise (ILE)
Length of time between exercise bouts

Locations

Country Name City State
United States University of Texas at Austin Human Performance Laboratory Austin Texas

Sponsors (1)

Lead Sponsor Collaborator
University of Texas at Austin

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary maximal leg power 10 min