NCT02695017

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
22

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2016

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 8, 2016

Completed
22 days until next milestone

First Posted

Study publicly available on registry

March 1, 2016

Completed
2 months until next milestone

Study Start

First participant enrolled

May 1, 2016

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2016

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2016

Completed
Last Updated

September 24, 2018

Status Verified

September 1, 2018

Enrollment Period

4 months

First QC Date

February 8, 2016

Last Update Submit

September 20, 2018

Conditions

Muscle OxigenationStrength

Outcome Measures

Primary Outcomes (1)

  • 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

Study Arms (2)

Iso inertial

EXPERIMENTAL

Subjects should do 12 exercise repetition with Iso inertial machine

Device: Iso inertial

Conventional machine

EXPERIMENTAL

Subjects should do 12 exercise repetition with conventional machine

Device: Conventional machine

Interventions

Iso inertialDEVICE
Iso inertial
Conventional machineDEVICE
Conventional machine

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Sedentary
  • No pain
  • Non disease

You may not qualify if:

  • Exercise experience

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centro Superior de Estudios Universitarios La Salle

Madrid, 28660, Spain

Location

Study Officials

  • Daniel Muñoz, MSc

    Centro La Salle Universitario

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Physiotherapist

Study Record Dates

First Submitted

February 8, 2016

First Posted

March 1, 2016

Study Start

May 1, 2016

Primary Completion

September 1, 2016

Study Completion

October 1, 2016

Last Updated

September 24, 2018

Record last verified: 2018-09

Data Sharing

IPD Sharing
Will share

Research publication

Locations

ES(1)