- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03011164
The Influence of Running and Velocity to Kinematic Parameters
Studieoversigt
Undersøgelsestype
Tilmelding (Forventet)
Kontakter og lokationer
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
i) 20< age < 30. ii) Body mass index < 30. iii) No history of major injury or surgery in lower limbs. iv) No symptoms of lower limbs. v) Physical examination to test the lower limbs to be normal. vi) The habit of moderate exercise (e.g. Jogging )at least once a week for at least 30 minutes
Exclusion Criteria:
i)Body mass index >30. ii) Injury or surgery in hip/knee/ankle. iii) History trauma in the lower limbs (e.g. fracture). iv) Neuropathic disease . v) Muscular disease. vi) Lack ability to finish the procedure physically or mentally. vii) Easy to fall. viii) Any other conditions that can influence gait parameters of the lower limbs.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
WV 1
The condition of this group will be set as participants walking at 3.5km/h
|
Once participants are eligible, they will undergo the experimental procedure.
Before data collection, they will walk or run on a treadmill in barefoot for ten minutes to adapt the condition.
The a gait analysis system will collect the data while they walk or run on the treadmill in barefoot at selected gait speed.
|
|
WV 2
The condition of this group will be set as participants walking at 4.0km/h
|
Once participants are eligible, they will undergo the experimental procedure.
Before data collection, they will walk or run on a treadmill in barefoot for ten minutes to adapt the condition.
The a gait analysis system will collect the data while they walk or run on the treadmill in barefoot at selected gait speed.
|
|
RV 1
The condition of this group will be set as participants running at 3.5km/h
|
Once participants are eligible, they will undergo the experimental procedure.
Before data collection, they will walk or run on a treadmill in barefoot for ten minutes to adapt the condition.
The a gait analysis system will collect the data while they walk or run on the treadmill in barefoot at selected gait speed.
|
|
RV 2
The condition of this group will be set as participants running at 4.0km/h
|
Once participants are eligible, they will undergo the experimental procedure.
Before data collection, they will walk or run on a treadmill in barefoot for ten minutes to adapt the condition.
The a gait analysis system will collect the data while they walk or run on the treadmill in barefoot at selected gait speed.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Kinematic characteristics of the the six-degree-of-motion (6DOF) of the gait at initial contact.
Tidsramme: 1 Day
|
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
|
1 Day
|
|
Kinematic characteristics of the the six-degree-of-motion (6DOF) of the gait at loading response.
Tidsramme: 1 Day
|
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
|
1 Day
|
|
Kinematic characteristics of the the six-degree-of-motion (6DOF) of the gait at mid-stance.
Tidsramme: 1 Day
|
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
|
1 Day
|
|
Kinematic characteristics of the the six-degree-of-motion (6DOF) of the gait at terminal stance.
Tidsramme: 1 Day
|
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
|
1 Day
|
|
Kinematic characteristics of the the six-degree-of-motion (6DOF) of the gait at initial swing.
Tidsramme: 1 Day
|
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
|
1 Day
|
|
Kinematic characteristics of the the six-degree-of-motion (6DOF) of the gait at mid-swing.
Tidsramme: 1 Day
|
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
|
1 Day
|
|
Kinematic characteristics of the the six-degree-of-motion (6DOF) of the gait at terminal swing.
Tidsramme: 1 Day
|
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
|
1 Day
|
|
The ranges of motion in the the six-degree-of-motion (6DOF) of the gait.
Tidsramme: 1 Day
|
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
|
1 Day
|
Samarbejdspartnere og efterforskere
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
Nøgleord
Andre undersøgelses-id-numre
- GuangzhouGH005
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 Walk and Run
-
Kansas State UniversityREI Cooperative Action FundRekrutteringFysisk aktivitet | Depression, angst | Selveffektivitet | Feasibility Pilotundersøgelse | Tid i naturenForenede Stater
-
University of California, San FranciscoUniversity of California, BerkeleyAfsluttet
-
Northwestern UniversityChicago Run; American Academy of Cerebral Palsy and Developmental Medicine og andre samarbejdspartnereTilmelding efter invitationCerebral Parese | Bruttomotorisk udviklingsforsinkelse | Motoriske lidelser | Myelomeningocele | ArthrogryposisForenede Stater
-
Izmir Democracy UniversityIkke rekrutterer endnu
-
Centre Hospitalier Universitaire de la RéunionIkke rekrutterer endnuVaskulær kognitiv svækkelse | Alzheimers sygdomGenforening
-
Lite Run Inc.Minneapolis Veterans Affairs Medical Center; TREATUkendtSlag | Hjerneskader, traumatiske | Rygmarvsskader | Gangforstyrrelser, neurologiske
-
Vilnius UniversityAfsluttetSund og rask | Stress | Angst | Psykisk nød | Trivsel | Mentalt helbred | Depressionslidelser | Kropsbevidsthed | VitalityLitauen
-
Gazi UniversityAfsluttet
-
Wake Forest University Health SciencesNational Council on Aging (NCOA)RekrutteringForebyggelse af faldForenede Stater
-
Arizona State UniversityNational Heart, Lung, and Blood Institute (NHLBI)RekrutteringHjertesygdomme | Diabetes mellitus | Fysisk aktivitet | Dyrke motion | Fysisk inaktivitetForenede Stater