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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02831036
Other study ID # SHEBA-16-3321-HS-CTIL
Secondary ID
Status Not yet recruiting
Phase N/A
First received July 10, 2016
Last updated July 10, 2016
Start date October 2016
Est. completion date April 2018

Study information

Verified date July 2016
Source Sheba Medical Center
Contact Haggai Schermann, M.D
Phone +972828771014
Email Haggai.Schermann@sheba.health.gov.il
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

20 healthy man, 10 in trial group and 10 in control group (randomly divided) will participate in the experiment on order to evaluate if improvement in physical fitness influences spatial learning in humans.


Description:

subjects in both groups will perform 4 sets of VO2max test and spatial orientation test with a month between them (total 3 month).

in addition, subjects in trial group will follow a training program throughout the trial (running on treadmill 3 times a week), suited according to their result in the first VO2max test.

in each set VO2max test will be perform before spatial orientation test , in order to evaluated the subject`s aerobic fitness. the spatial orientation test is composed of 5 following days in which the subject has 3 attempts to arrive to a destination in xbox one controller using a virtual glasses (Oculus Rift DK2). each attempt duration is 2 min.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date April 2018
Est. primary completion date October 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- civilian healthy man, aged 18-30

- without any neurological or psychiatric disorder

- not wearing eyeglasses

Exclusion Criteria:

- athletes or trained man (for both groups)

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Other:
training program
subjects in the trial group will follow a training program which includes 3 times a week running on a treadmill.
VO2max test
each subject will perform 4 times VO2max test according to BRUCE protocol in order to evaluate his aerobic fitness.
spatial orientation test
each subject will undergo 4 spatial orientation tests during the trial (month between 2 tests), each test is composed of 5 following days in which the subject will wear virtual reality glasses (Oculus Rift DK2) and attempt to arrive different destinations in a virtual maze tasks (using xbox one controller). each day will be given 3 attempts, the duration of each attempt is 2 min.

Locations

Country Name City State
Israel Sheba medical center Tel-Hashomer Ramat- Gan

Sponsors (2)

Lead Sponsor Collaborator
Sheba Medical Center Bar-Ilan University, Israel

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary spatial learning (composite) each spatial orientation test length is 5 days. spatial learning is evaluated through time for completion and number of errors out of 3 attempts each day. 20 experimental days for each participant No
Secondary maximal aerobic capacity VO2max tests along the trial are performed in order to evaluate the improvement or lack of improvement in both groups in correlation with their spatial learning. 4 experimental days for each participant No
See also
  Status Clinical Trial Phase
Completed NCT03758586 - Spatial Skill Training for Robot-assisted Surgery N/A