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Autonomic Modulation in Athletes and Non-Athletes With Spinal Cord Injury During Task in Virtual Reality Environment

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04618003
Recruitment Status : Completed
First Posted : November 5, 2020
Last Update Posted : November 5, 2020
Sponsor:
Information provided by (Responsible Party):
Talita Dias da Silva, University of Sao Paulo

Brief Summary:
The study consisted in the analysis of the autonomic modulation of the heart rate by the Heart Rate Variability of the participants at rest for 5 minutes, and during physical activity of 8 minutes, through a virtual reality game. The data capture was performed using a cardio-frequency meter with belt placed on the volunteer's trunk and, in addition, questionnaires, functional classification scales and personal data collection were applied.

Condition or disease Intervention/treatment
Spinal Cord Injuries Behavioral: Adaptation of autonomic nervous system to activity in virtual reality

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Study Type : Observational
Actual Enrollment : 145 participants
Observational Model: Case-Control
Time Perspective: Cross-Sectional
Official Title: Analysis of Autonomic Modulation in Athletes and Non-Athletes With Spinal Cord Injury During Task in Virtual Reality Environment
Actual Study Start Date : March 1, 2017
Actual Primary Completion Date : August 1, 2018
Actual Study Completion Date : August 1, 2020

Resource links provided by the National Library of Medicine


Group/Cohort Intervention/treatment
Athletes with Spinal Cord Injury
Group of athletes with spinal cord injury that was assessed at rest and during a physical activity in virtual reality.
Behavioral: Adaptation of autonomic nervous system to activity in virtual reality
heart rate variability assessed at rest and during a physical activity in virtual reality.

Non-athletes with spinal cord injury
Group of non-athletes with spinal cord injury that was assessed at rest and during a physical activity in virtual reality.
Behavioral: Adaptation of autonomic nervous system to activity in virtual reality
heart rate variability assessed at rest and during a physical activity in virtual reality.

Able-bodied control group
Group of non-athletes able-bodied control subjects that was assessed at rest and during a physical activity in virtual reality.
Behavioral: Adaptation of autonomic nervous system to activity in virtual reality
heart rate variability assessed at rest and during a physical activity in virtual reality.




Primary Outcome Measures :
  1. Cardiac autonomic modulation is different between athletes and non athletes with spinal cord injury (SCI), bu no differences between athletes with SCI and able-bodied controls. [ Time Frame: 1 day ]
    Athletes with SCI present a better cardiac autonomic modulation then non-athletes with SCI, assessed through linear and non-linear heart rate variability indices at rest and during VR activity

  2. Athletes and able-bodied subjects present a good adaptation of autonomic nervous system than non-athletes with spinal cord injury. [ Time Frame: 1 day ]
    Athletes and able-bodied controls present a good adaptation of autonomic nervous system assessed through indices of heart rate variability. i.e. parasympathetic withdraw during physical activity in Virtual Reality, but with no significant difference for non-athletes with spinal cord injury.



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Ages Eligible for Study:   18 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
The study included athletes and non-athletes with a confirmed medical diagnosis of SCI, with voluntary extension of elbows and wrist, active trunk control, and who had already completed rehabilitation. For the athlete group, participants had to fulfill the minimum criteria for defining an active athlete, described in the next section. Also, a control group of able-bodied subjects, approximately paired by age and sex wit the and non-athlete groups were recruited.
Criteria

Inclusion Criteria:

  • Confirmed medical diagnosis of SCI
  • Preserved motor activity for extension of the upper limbs and active trunk control, which had already finished their process of adaptation to injury.

Exclusion Criteria:

  • Functional incapacities of the upper limbs to perform the game,
  • Diagnosis of heart disease or other neurological disorders not due to SCI,
  • Consumption of drugs that are not part of their usual treatment routine and that influence the cardiac and nervous systems,
  • Error greater than 5% in the analysis of HRV.

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): NCT04618003


Locations
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Brazil
Comitê de Ética e Pesquisa da Universidade Federal de São Paulo
São Paulo, SP, Brazil, 04023-900
Sponsors and Collaborators
University of Sao Paulo
Investigators
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Principal Investigator: Talita D Silva, Ph.D. University of Sao Paulo
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Talita Dias da Silva, Researcher, University of Sao Paulo
ClinicalTrials.gov Identifier: NCT04618003    
Other Study ID Numbers: 79346017.8.0000.5505
First Posted: November 5, 2020    Key Record Dates
Last Update Posted: November 5, 2020
Last Verified: October 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Spinal Cord Injuries
Wounds and Injuries
Spinal Cord Diseases
Central Nervous System Diseases
Nervous System Diseases
Trauma, Nervous System