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Evaluation of Physical and Cognitive Performance After Simulated Road March Combines Physical and Cognitive Load Using a Virtual Reality Environment

S

Sheba Medical Center

Status

Unknown

Conditions

Physical Examination

Treatments

Other: protocol of using CAREN and MOTEK systems

Study type

Interventional

Funder types

Other

Identifiers

NCT02644213
SHEBA-15-2664-OF-CTIL

Details and patient eligibility

About

The aim of the research is to evaluate the influence of physical and cognitive load as pre-mission activity on the soldier's physical and cognitive performance, in compare to physical load alone.

In order to do so, 12 healthy subjects will perform stimulated road march using a virtual reality environment combined with cognitive load and without, and their physical and cognitive performance will be evaluated by tests before and after.

Full description

12 young, healthy civilian volunteers will participate in this study. After reading and signing an informed consent form, all subjects will undergo medical examination which includes ECG, anthropometric measurements and Vo2max test.

Afterwards, the subjects will perform randomly 3 experimental days, each consist of physical and cognitive performance evaluation before and after simulated road march using a virtual reality environment; once without additional load, once combining cognitive load during the road march, and once without physical load (without march, waiting between evaluations) as control.

The experiment will take place in a dome room, and the systems being used are:

  1. CAREN high (Computer Assisted Rehabilitation Environment) which screens virtual scene in the dome.
  2. MOTEK (Motek Medical©, the Netherlands) which is a two track treadmill (for each leg) placed on a rotatable platform.

cognitive tasks for example: navigation, identification and remembering cars/aircraft.

Physical and cognitive performance will be evaluated at each experimental day, before and after performing the protocol. at the end of the march, cognitive performance will be evaluated by validated tests on laptop (SYNWIN activity research services) and executive function evaluation based on Trail Making Test (TMT), afterwards, Physical performance will be evaluated by HRV and time to exhaustion test (30 min after the end of cognitive tests).

Enrollment

12 estimated patients

Sex

Male

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • aged 18-30
  • healthy civilians volunteers
  • with no background illnesses
  • with history of combat unit service in the IDF.
  • fit to perform 10 Km moderate march while carrying load.

Exclusion criteria

  • The existence or suspicion of existing cardiac or respiratory disease.
  • Hypertension.
  • Diabetes.
  • Any muscles or skeleton condition.
  • Any hormonal disease or any other chronic illness that may inhibit participation in the experiment.
  • Infectious disease 3 days prior to the experiment.

Trial design

12 participants in 1 patient group

research arm
Experimental group
Description:
12 young, healthy civilian volunteers will participate in this study. The experiment will take place in a dome room. The experiment will be performed according to the protocol of using CAREN and MOTEK systems: 1. CAREN high (Computer Assisted Rehabilitation Environment) which screens virtual scene in the dome. 2. MOTEK (Motek Medical©, the Netherlands) which is a two track treadmill (for each leg) placed on a rotatable platform. each subject will undergo the same experiment protocol.
Treatment:
Other: protocol of using CAREN and MOTEK systems

Trial contacts and locations

1

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Central trial contact

Ofir Frenkel, M.D

Data sourced from clinicaltrials.gov

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