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Changes in Oxygen Saturation in Two Exercise Modalities

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ClinicalTrials.gov Identifier: NCT02695017
Recruitment Status : Completed
First Posted : March 1, 2016
Last Update Posted : September 24, 2018
Sponsor:
Information provided by (Responsible Party):
Daniel Muñoz-Garcia, Centro Universitario La Salle

Brief Summary:
The investigator will proceed to assess changes in oxygenation of muscle tissue, electromyographic activation and strength in healthy subjects. For this, a measurement of all demographic variables on the first day of the study as well as a familiarity with the equipment will be performed. Participants will start the intervention 48 hours later to proceed with the first intervention with one of the exercises in this research (inertial pulley or regular machine). Later on, 48 hours later participants will perform the latest intervention that has not yet done, thus generating a crossover study.

Condition or disease Intervention/treatment Phase
Muscle Oxigenation Strength Device: Iso inertial Device: Conventional machine Not Applicable

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 22 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Basic Science
Official Title: Comparison of Changes in Oxygen Saturation in Flywheel Exercise Versus Conventional Strength Machine
Study Start Date : May 2016
Actual Primary Completion Date : September 2016
Actual Study Completion Date : October 2016

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Iso inertial
Subjects should do 12 exercise repetition with Iso inertial machine
Device: Iso inertial
Experimental: Conventional machine
Subjects should do 12 exercise repetition with conventional machine
Device: Conventional machine



Primary Outcome Measures :
  1. Percentage of Oxygen saturation of Vastus lateralis muscle during the exercise of each participant [ Time Frame: one second ]
    physiological parameter (Percentage of local oxygen consume will be record in every stage of the investigation)



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Ages Eligible for Study:   18 Years to 30 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Sedentary
  • No pain
  • Non disease

Exclusion Criteria:

  • Exercise experience

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02695017


Locations
Spain
Centro Superior de Estudios Universitarios La Salle
Madrid, Spain, 28660
Sponsors and Collaborators
Centro Universitario La Salle
Investigators
Principal Investigator: Daniel Muñoz, MSc Centro La Salle Universitario

Responsible Party: Daniel Muñoz-Garcia, Physiotherapist, Centro Universitario La Salle
ClinicalTrials.gov Identifier: NCT02695017     History of Changes
Other Study ID Numbers: CSEULS-PI-086
First Posted: March 1, 2016    Key Record Dates
Last Update Posted: September 24, 2018
Last Verified: September 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: Research publication