bèta
Trial Radar AI
De klinische studie NCT06404268 voor Beroerte is recruterend. Bekijk de kaartweergave van de Klinische Studies Radar en de AI-ontdekkingstools voor alle details. Of stel hier een vraag.
Eén studie komt overeen met de filtercriteria
Kaartweergave

Facilitating Neuroplastic Changes of Acute Stroke Survivors

Recruterend
Informatie over klinische studies is voornamelijk in het Engels beschikbaar. Trial Radar AI kan echter helpen! Klik op 'Leg studie uit' om de informatie over de studie te bekijken en te bespreken in de taal van uw keuze.
De klinische studie NCT06404268 onderzoekt behandeling bij Beroerte. Deze Fase 1 Fase 2 interventioneel-studie heeft de status recruterend. Het doel is om 68 deelnemers te includeren vanaf 1 juni 2025. De studie wordt geleid door de Universiteit van Maryland, Baltimore en de voltooiing is gepland op 31 augustus 2028. Laatste update op ClinicalTrials.gov: 9 juli 2025.
Beknopte samenvatting
This project will develop a wearable rehabilitation robot suitable for in-bed acute stage rehabilitation. It involves robot-guided motor relearning, passive and active motor-sensory rehabilitation early in the acute stage post-stroke including patients who are paralyzed with no motor output. The early acute stroke rehabilitation device will be evaluated in this clinical trial.
Uitgebreide beschrijving
Stroke survivors often experience loss of motor control and impaired function. Immediately after stroke, there is a time-limited window of heightened plasticity during which the greatest gains in recovery occur. Therefore, early intensive sensorimotor rehabilitation post-stroke is critical in improving functional outcomes and minimizing disability. However, acute stroke survivors often receive little active training to improve mobility during their hospital stay and they are left alone during most of the day. Especially for those acute patients with no voluntary motor output, active motor training might be even less, partly due to a lack of rehabilitation protocols to detect potential motor recovering signals sensitively and facilitate neuroplastic changes. To address this unmet clinical need, this project will develop a novel wearable rehabilitation robot suitable for in-bed acute stage rehabilitation with guided motor relearning, passive and active motor-sensory rehabilitation early in the acute stage post-stroke including patients who are paralyzed with no motor output. The early acute stroke rehabilitation device will be evaluated in this clinical trial.
Officiële titel

Facilitating Neuroplastic Changes of Acute Stroke Survivors With Severe Hemiplegia

Aandoeningen
Beroerte
Publicaties
Wetenschappelijke artikelen en onderzoekspapers gepubliceerd over deze klinische studie:
Toon meer
Andere studie-ID's
  • HP-00110205
NCT-ID
Startdatum (Werkelijk)
2025-06-01
Laatste update geplaatst
2025-07-09
Verwachte einddatum
2028-08-31
Inschrijving (Geschat)
68
Studietype
Interventioneel
FASE
Fase 1
Fase 2
Status
Recruterend
Trefwoorden
Stroke
Paraplegia
Acute
Primaire doel
Behandeling
Toewijzing
Gerandomiseerd
Interventiemodel
Parallel
Blindering
Enkelblind
Armen / Interventies
Deelnemersgroep/StudiearmInterventie/Behandeling
ExperimenteelStudy group - Wearable ankle robot rehab
Wearable rehab robot with motor relearning with real-time feedback, passive stretching under intelligent control; Active movement training with robotic assistance
Motor Relearning Training
Ankle motor control relearning training under real-time feedback
Passief stretchen
Passive stretching under intelligent robotic control
Gamed-based Active Movement Training
Active movement training through movement games with robotic assistance
Actieve comparatorControl group - Limited wearable ankle robot rehab
The same wearable robot used by the study group will be used for the control group but in a limited way: no motor relearning training under real-time feedback; passive movement in the joint middle range of motion instead of passive stretching; active movement training with no robotic assistance
Passieve beweging
Passive movement in the joint middle range of motion
Active Movement Training
Active movement training without robotic assistance
Ankle Torque and Motion Measurement
Ankle torque and motion measurement with no real-time feedback
Primaire uitkomst
UitkomstmaatBeschrijving van de uitkomstmaatTijdsbestek
Fugl-Meyer Lower Extremity (FMLE)
The Fugl-Meyer Lower Extremity (FMLE) assessment is a measure of lower extremity (LE) motor and sensory impairments. The FMLE scale ranges from 0 to 34, with higher scores indicating better motor function.
At the beginning and end of 3-week training, and 1 month after the treatment ends]
Secundaire uitkomst
UitkomstmaatBeschrijving van de uitkomstmaatTijdsbestek
Active range of motion (AROM)
AROM will be measured in degrees in the ankle joint while subjects use the muscles to move the ankle.
At the beginning and end of 3-week training, and 1 month after the treatment ends
Passive Range of Motion (PROM) will be measured in degrees in the ankle joint while the robot moves the ankle of the subject strongly.
Passive Range of Motion PROM will be measured in degrees in the ankle joint while the robot moves the ankle of the subject strongly.
At the beginning and end of 3-week training, and 1 month after the treatment ends
Strength of the ankle flexor-extensor muscle will be measured in Newtons
Strength of the ankle flexor-extensor muscle will be measured in Newtons
At the beginning and end of 3-week training, and 1 month after the treatment ends
Modified Ashworth Scale (MAS)
The Modified Ashworth Scale is the most widely used assessment tool to measure resistance to limb movement in a clinic setting. Scores range from 0-4, with 6 choices. 0 (0) - No increase in muscle tone; 1 (1) - Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension; 1+ (2) - Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM (range of movement); 2 (3) - More marked increase in muscle tone through most of the ROM, but affect part(s) easily moved; 3 (4) - Considerable increase in muscle tone passive, movement difficult; 4 (5) - Affected part(s) rigid in flexion or extension.
At the beginning and end of 3-week training, and 1 month after the treatment ends
Berg Balance Scale
The Berg balance scale is used to objectively determine a patient's ability (or inability) to safely balance during a series of predetermined tasks. The Berg balance scale ranges from 0 to 56. It is a 14-item list with each item consisting of a five-point ordinal scale ranging from 0 to 4, with 0 indicating the lowest level of function and 4 the highest level of function.
At the beginning and end of 3-week training, and 1 month after the treatment ends
10-meter Walk Test
The 10 Meter Walk Test is a performance measure used to assess walking speed in meters per second over a short distance at the beginning and end of 3-week training, and 1 month after the treatment ends. It can be employed to determine functional mobility and gait function.
At the beginning and end of 3-week training, and 1 month after the treatment ends
Geschiktheidscriteria

Leeftijd van deelnemers
Volwassene, Oudere volwassene
Minimumleeftijd
30 Years
Geslachten die in aanmerking komen voor de studie
Allen
  • Acute first time unilateral hemispheric stroke (hemorrhagic or ischemic stroke, 24 hours after admission to 1 month post-stroke at the start of the proposed treatment)
  • Hemiplegia or hemiparesis
  • 0≤Manual Muscle Testing (MMT)<=2
  • Age 30-85
  • Ankle impairments including stiff calf muscles and/or inadequate dorsiflexion

  • Medically not stable
  • Associated acute medical illness that interferes with ability to training and exercise
  • No impairment or very mild ankle impairment of ankle
  • Severe cardiovascular problems that interfere with ability to perform moderate movement exercises
  • Cognitive impairment or aphasia with inability to follow instructions
  • Severe pain in legs
  • Severe ankle contracture greater than 15° plantar flexion (when pushing ankle to dorsiflexion)
  • Pressure ulcer, recent surgical incision or active skin disease with open wounds present below knee
University of Maryland, Baltimore logoUniversiteit van Maryland, Baltimore200 actieve klinische studies om te verkennen
The University of Texas Health Science Center, Houston logoThe University of Texas Health Science Center, Houston
Verantwoordelijke instantie
Li-Qun Zhang, Hoofdonderzoeker, Professor, University of Maryland, Baltimore
Centraal Contactpersoon
Contact: Soh-Hyun Hur, 410 706-8625, [email protected]
2 Studielocaties in 1 landen

Maryland

University of Maryland Baltimore, Baltimore, Maryland, 21201, United States
Dali Xu, PhD, Contact
Peiwen Fu, BS, Contact
Recruterend
UMROI, Baltimore, Maryland, 21207, United States
Dali Xu, Contact
Peiwen Fu, Contact
Recruterend