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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02695017
Other study ID # CSEULS-PI-086
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 2016
Est. completion date October 2016

Study information

Verified date September 2018
Source Centro Universitario La Salle
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date October 2016
Est. primary completion date September 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- Sedentary

- No pain

- Non disease

Exclusion Criteria:

- Exercise experience

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Iso inertial

Conventional machine


Locations

Country Name City State
Spain Centro Superior de Estudios Universitarios La Salle Madrid

Sponsors (1)

Lead Sponsor Collaborator
Centro Universitario La Salle

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of Oxygen saturation of Vastus lateralis muscle during the exercise of each participant physiological parameter (Percentage of local oxygen consume will be record in every stage of the investigation) one second
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