- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01774110
Evaluation of Early Standardized Task-Specific Training (ESTT) (ESTT)
1 september 2015 uppdaterad av: Karen McCain, University of Texas Southwestern Medical Center
Evaluation of Early Standardized Task-Specific Training (ESTT) in Persons With Acute Stroke
A. Specific Aims:
1. There is one specific aim of this study. The aim is to evaluate the effectiveness of early standardized task-specific training (ESTT) in persons with acute stroke.
B. Hypothesis:
1. It is our hypothesis that subjects who receive ESTT will walk faster and more symmetrically than published reports of gait outcomes in persons with stroke.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
It is our contention that gait recovery after stroke is impacted by the interventions that are acutely utilized during training.
There is not a consensus about how to most effectively train individuals after stroke.
It is clear, however, that most persons are left with significant and often debilitating gait dysfunction after stroke so there is an urgent need to find more effective therapeutic methods.
Studietyp
Interventionell
Inskrivning (Faktisk)
12
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
Texas
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Austin, Texas, Förenta staterna, 78705
- St. David's Rehabilitation Hospital
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Dallas, Texas, Förenta staterna, 75246
- Baylor Institute for Rehabilitation - Dallas
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Dallas, Texas, Förenta staterna, 75247
- Baylor Institute for Rehabilitation - Northwest
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Frisco, Texas, Förenta staterna, 75034
- Baylor Institute for Rehabilitation - Frisco
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
16 år till 80 år (Barn, Vuxen, Äldre vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- Recent stroke (less than 6 weeks)
- Able to give conformed consent or have family member who can give consent
- first time stroke OR complete recovery from prior stroke
Exclusion Criteria:
- non-ambulatory before onset of stroke
- bilateral stroke
- presence of severe cardiac problems
- other co-morbidities which would affect gait training (i.e. amputation, spinal cord injury, traumatic brain injury, etc.)
- recent myocardial infarct (within 4 weeks)
- any uncontrolled health condition for which exercise is contraindicated
- severe lower extremity joint disease/pathology that would interfere with gait training
- subjects with BMI greater than 40
- significant cognitive impairment
- age greater than 80 years or less than 16 years
- able to complete 5 or more full heel raises with the affected ankle in standing with the knee extended with no more than one or two fingers on support surface for balance
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
---|---|
Experimentell: early standardized task training
Persons in the experimental group will receive ESTT (early standardized task specific training) for gait treatment after stroke.
|
Early standardized task training is a treatment approach using treadmill training applied very early after stroke onset.
Andra namn:
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Change in Walking Velocity From Initial Assessment to Completion of Study at 6 Months Post Enrollment
Tidsram: This will be done at the time of discharge from inpatient rehabilitation (the initial assessment point of the study) and at 6-months post enrollment.
|
Computerized gait analysis is done by a mat system (GAITRite) that electronically calculates the velocity.
|
This will be done at the time of discharge from inpatient rehabilitation (the initial assessment point of the study) and at 6-months post enrollment.
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Change in Score on Stroke Rehabilitation Assessment of Movement (STREAM) Test From Initial Assessment to Discharge From Study.
Tidsram: This test will be done at the initiation of the protocol (initial assessment) and at 6 months post enrollment
|
The Stroke Rehabilitation Assessment of Movement (STREAM) is a test of motor recovery after stroke.
There are 3 subsections of the test, an upper extremity section, a lower extremity section and a mobility section.
Each section is scored independently and is normed to 100 points.
Each of the 3 sections is then combined into a total overall function score which is also normed to 100.
Therefore, a score of 100 represents full recovery whereas a score of 50 represents about 50% recovery from the stroke.
|
This test will be done at the initiation of the protocol (initial assessment) and at 6 months post enrollment
|
Andra resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Change in 6-Minute Walk Test Distance From Time of Discharge From Rehabilitation (Initial Assessment) to 6 Months Post Enrollment
Tidsram: This test will be done at the initiation of the protocol (initial assessment) and at 6 months post enrollment
|
The 6-Minute Walk Test is a test of walking endurance and walking velocity.
|
This test will be done at the initiation of the protocol (initial assessment) and at 6 months post enrollment
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Utredare
- Huvudutredare: Karen J McCain, PT, DPT, NCS, UT Southwestern Medical Center
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 augusti 2012
Primärt slutförande (Faktisk)
1 december 2014
Avslutad studie (Faktisk)
1 december 2014
Studieregistreringsdatum
Först inskickad
18 januari 2013
Först inskickad som uppfyllde QC-kriterierna
18 januari 2013
Första postat (Uppskatta)
23 januari 2013
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
1 oktober 2015
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
1 september 2015
Senast verifierad
1 september 2015
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- ESTT
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .
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