- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02831036
The Impact of Physical Exercise on Navigation Performance in Soldier
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Tilmelding (Forventet)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
Ramat- Gan
-
Tel-Hashomer, Ramat- Gan, Israel
- Sheba Medical Center
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
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)
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Eksperimentel: trial group
subjects in trial group will be following the experimental protocol (VO2max tests and spatial orientation tests) while performing a training program during the trial (3 months).
|
subjects in the trial group will follow a training program which includes 3 times a week running on a treadmill.
each subject will perform 4 times VO2max test according to BRUCE protocol in order to evaluate his aerobic fitness.
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.
|
Andet: control group
following the experimental protocol (VO2max tests and spatial orientation tests)without performing additional exercise.
|
each subject will perform 4 times VO2max test according to BRUCE protocol in order to evaluate his aerobic fitness.
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.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
spatial learning (composite)
Tidsramme: 20 experimental days for each participant
|
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
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
maximal aerobic capacity
Tidsramme: 4 experimental days for each participant
|
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
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- SHEBA-16-3321-HS-CTIL
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Rumlig læring
-
RenJi HospitalIkke rekrutterer endnuAnvendelse af kunstig intelligens Deep Learning-teknologi i magnetisk resonans lumbal billeddannelseDeep Learning, Lumbal Magnetic Resonance Imaging
-
Rutgers, The State University of New JerseyRekrutteringSpatial NavigationForenede Stater
-
Hand & Reconstructive MicrosurgeryAfsluttetMasselæring, Spaced Learning, Mikrokirurgi
-
University of Illinois at Urbana-ChampaignAfsluttetKognitiv forandring | Behandling, Visual SpatialForenede Stater
-
Charite University, Berlin, GermanyEuropean Space Agency; University of California; Simon Fraser University; University... og andre samarbejdspartnereAktiv, ikke rekrutterendeVirtual reality | Isolation, social | Spatial NavigationDen Russiske Føderation
-
University of Illinois at Urbana-ChampaignAfsluttetKognitiv forandring | Arbejdshukommelse | Hæmning (psykologi) | Behandling, Visual SpatialForenede Stater
-
University of Geneva, SwitzerlandRekrutteringUnilateral Spatial ForsømmelseSchweiz
-
HITEC-Institute of Medical SciencesAfsluttetOSCE (Objective Structured Clinical Examination) | TBL (Team Based Learning) | Undervisning af kliniske færdigheder til medicinske studerendePakistan
-
Istituto Auxologico ItalianoAfsluttet
-
Istituto Auxologico ItalianoAktiv, ikke rekrutterendeSpatial NavigationItalien
Kliniske forsøg med training program
-
Columbia UniversityWorld Bank; United NationsAfsluttet
-
Matrouh UniversityAfsluttetViden, holdninger, praksis | InterventionEgypten
-
Northwestern UniversityGeorgetown UniversityTilmelding efter invitationKroniske nyresygdomme | Genetisk dispositionForenede Stater
-
Stony Brook UniversityNorthwell Health; Department of Health and Human Services; Rutgers UniversityAfsluttet
-
Savannas Forever TanzaniaNational Institute for Medical Research, Tanzania; Arusha Lutheran Medical...UkendtBørnemishandlingTanzania
-
Anna HooverNational Institute of Environmental Health Sciences (NIEHS)RekrutteringDesinfektionsbiprodukterForenede Stater
-
Memorial Sloan Kettering Cancer CenterMARTELL FOUNDATIONAktiv, ikke rekrutterende
-
NYU Langone HealthRekrutteringKræft i bugspytkirtlenForenede Stater
-
University of Wisconsin, MadisonChan Zuckerberg InitiativeAktiv, ikke rekrutterende
-
University of TorontoUkendt