- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT00127439
Effects of Robotic Versus Manually-Assisted Locomotor Training for Individuals With Incomplete Spinal Cord Injury (DE)
Differential Effects of Robotic vs. Manually-Assisted Locomotor Training
Přehled studie
Postavení
Podmínky
Detailní popis
Spinal cord injury (SCI) is one of the most disabling health problems facing adults today, with one of the consequences often being inability to walk or difficulty walking. Recent studies suggest that intensive step training on a treadmill using body-weight support (BWS) and manual assistance that provides repetitive task-specific sensory cues to the neural axis can improve the recovery of walking for persons with incomplete SCI. More recently, robotics have been developed as an alternative to manually-assisted training. Robotic-assisted training may allow for increased intensity of training, improve the reproducibility and consistency of training, and reduce the personnel needed to implement the training. However, the effects of robotic-assisted training compared to manually-assisted training are not known. An improved understanding of these differential effects and the mechanisms of improvement in walking can facilitate continued advances in evidenced-based practice of neuro-rehabilitation, therefore improving the treatment of persons with SCI.
The primary objective of this project is to assess and compare the effects of robotic-assisted versus manually-assisted locomotor training (LT) using the body-weight support (BWS) on sub-tasks of walking. Specifically, we believe that at least four sub-tasks of walking are differentially affected by the robotic-assisted training when compared to manually-assisted training (propulsion, transition from stance to step, stepping, and equilibrium). The investigators hypothesize that robotic-assisted training will have a greater effect on improving propulsion, transition and equilibrium. The effect of these two modalities on adaptability, a fifth sub-task of walking, is unclear; therefore, a development component of the pilot project will involve establishing a quantitative measure of adaptability and assessing differential effects of training. Participants will be randomized to one of two training groups: robotic-assisted or manually-assisted, and evaluated for performance on sub-tasks of walking.
Typ studie
Zápis (Aktuální)
Fáze
- Nelze použít
Kontakty a umístění
Studijní místa
-
-
Florida
-
Gainesville, Florida, Spojené státy, 32608
- North Florida/South Georgia Veterans Health System
-
-
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Popis
Inclusion Criteria:
- Adults at least 18 years of age
- Spinal cord injury (SCO) at least 6 months since injury
- Motor I-SCI, upper motor neuron lesion only at cervical or thoracic levels
- A diagnosis of first time SCI including etiology from trauma, vascular, or orthopedic pathology
- SCI as defined by the American ASIA Impairment Scale categories C or D
- Medically stable condition that is asymptomatic for bladder infection, decubiti, osteoporosis, cardiopulmonary disease, pain, contractures or other significant medical complications that would prohibit or interfere with testing of walking function and training or alter compliance with the training protocol
- Documented medical approval from the participant's personal physician verifying the participant's medical status at time of enrollment
- Ability to walk a minimum of 30 feet with or without an assistive device, independently or with minimal assistance
- Over ground gait speed < 0.8 m/s
- Persons using anti-spasticity medication must maintain stable medication dosage during the study
- Able to give informed consent
Exclusion Criteria:
- Current participation in a rehabilitation program/research protocol that could interfere or influence the outcome measures of the current study
- History of congenital SCI (e.g. myelomeningocele, intraspinal neoplasm, Friedreich's ataxia) or other degenerative spinal disorders (e.g. spinocerebellar degeneration, syringomyelia) that may complicate the protocol
- Inappropriate or unsafe fit of the harness or robotic trainer due to the participant's body size and/or joint contractures or severe spasticity that would prohibit the safe provision of either training modality
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Randomizované
- Intervenční model: Paralelní přiřazení
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
---|---|
Experimentální: Robotic Assisted Locomotor Training
A robotic stepping device in concert with a body weight support system and treadmill is used by a physical therapist and trainers for the participant with spinal cord injury to intensely practice task-specific standing and stepping to advance retraining the capacity to step.
The robotic device provides the appropriate kinematics associated with standing and stepping.
|
The total program is 45 sessions, 5x/week with total locomotor training (LT) duration of 30 stepping minutes/day.
1) BWS is initiated at 40% and gradually decreasing to 0%, 2) treadmill speed is set at normal walking speeds and increased as tolerated, and 3) manual assistance given when the subject is unable to independently step or control upright posture, and decreased as participant progresses.
Trainers assist via verbal cues and manual assistance to achieve good stepping.
The goal for endurance is 20 mins of continuous, independent, coordinated stepping on the treadmill at 0% BWS.
Participants are encouraged to assist and/or independently maintain an upright posture, weight shift onto the loaded limb, flex or extend their legs, and to swing their arms in coordination with the legs.
Ostatní jména:
|
Experimentální: Manually Assisted Locomotor Training
A body weight support system and treadmill is used by a physical therapist and trainers for the participant with spinal cord injury to intensely practice task-specific standing and stepping to advance retraining the capacity to step.
Therapists and trainers promote the appropriate kinematics associated with standing and stepping.
|
The total program is 45 sessions, 5x/week with total locomotor training (LT) duration of 30 stepping minutes/day.
1) BWS is initiated at 40% and gradually decreasing to 0%, 2) treadmill speed is set at normal walking speeds and increased as tolerated, and 3) manual assistance given when the subject is unable to independently step or control upright posture, and decreased as participant progresses.
Trainers assist via verbal cues and manual assistance to achieve good stepping.
The goal for endurance is 20 mins of continuous, independent, coordinated stepping on the treadmill at 0% BWS.
Participants are encouraged to assist and/or independently maintain an upright posture, weight shift onto the loaded limb, flex or extend their legs, and to swing their arms in coordination with the legs.
Ostatní jména:
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
---|---|---|
Self Selected Velocity on Treadmill
Časové okno: 12 weeks
|
Subjects walk on a treadmill with overhead safety mounted to laboratory ceiling while wearing a harness.
Treadmill speeds adjusted to lower than overground walking speeds and adjusted to patient reaches a comfortable speed.
|
12 weeks
|
Stepping: Foot Trajectory Toe-Off
Časové okno: 12 weeks
|
Foot angle in a global reference frame at the start of swing phase during treadmill walking at self-selected speed.
The kinematic outcomes were first standardized as deviations from control subjects who walk at similar speed (i.e., deviation from the control mean divided by SD among control).
Stepping was quantified by the change in orientation of the foot angle (in a global reference frame) from the beginning to the end of the swing phase (i.e., foot-off to foot-down).
The values will be identified from the processed 3-D kinematics for each walking cycle and average across steps.
|
12 weeks
|
Stepping: Foot Trajectory Toe-off % Cycle
Časové okno: 12 weeks
|
The outcome measure is the percentage of the gait cycle (%) for the occurrence of toe off.
Foot trajectory toe-off was identified as indicated in the prior primary outcome (#2).
The occurrence of toe-off was then identified relative to the percent of a complete gait cycle and thus the end point of the stance component of the gait cycle and the point of initiation for the swing component of the gait cycle.
This outcome is reported in per cent of gait cycle.
|
12 weeks
|
Foot Trajectory Initial Contact
Časové okno: 12 weeks
|
Foot trajectory initial contact is the foot angle in a global reference frame at the end of swing (start of stance phase) during treadmill walking at self-selected speed when the foot contacts the ground (i.e.
heel strike, foot contact, initial contact).
The kinematic outcomes were first standardized as deviations from control subjects who walk at similar speed (i.e.
deviation from the control mean divided by the SD among control).
Foot trajectory initial contact (heel strike) was quantified by the orientation of the foot angle (in a global reference frame) at foot down (initial contact or heel strike).
The values will be identified from the process 3-D kinematics for each walking cycle and averaged across steps.
The outcome measurement is in degrees.
|
12 weeks
|
Foot Trajectory Range (Toe Off to Heel Strike)
Časové okno: 12 weeks
|
Range of foot trajectory from toe off to heel strike in degrees.
The kinematic outcomes were first standardized as deviations from control subjects who walk at similar speed (i.e., deviation from the control mean divided by SD among control).
|
12 weeks
|
Propulsion: Propulsive Impulse
Časové okno: 12 weeks
|
Push-off force at toe off in N-s during treadmill stepping
|
12 weeks
|
Kinematics: Minimum Thigh Angle
Časové okno: 12 weeks
|
Greatest thigh angle for hip flexion during stepping
|
12 weeks
|
Kinematics: Minimum Hip Angle - Extension
Časové okno: 12 weeks
|
Hip angle at maximal hip extension during stepping
|
12 weeks
|
Kinematics: Trunk Angle Mid-Stance
Časové okno: 12 weeks
|
Trunk Angle Mid-Stance - position in degrees
|
12 weeks
|
Spolupracovníci a vyšetřovatelé
Vyšetřovatelé
- Vrchní vyšetřovatel: Andrea Behrman, PT PhD, North Florida/South Georgia Veterans Health System
Publikace a užitečné odkazy
Obecné publikace
- Behrman AL, Harkema SJ. Locomotor training after human spinal cord injury: a series of case studies. Phys Ther. 2000 Jul;80(7):688-700.
- Barbeau H, Norman K, Fung J, Visintin M, Ladouceur M. Does neurorehabilitation play a role in the recovery of walking in neurological populations? Ann N Y Acad Sci. 1998 Nov 16;860:377-92. doi: 10.1111/j.1749-6632.1998.tb09063.x.
- Hesse S, Uhlenbrock D. A mechanized gait trainer for restoration of gait. J Rehabil Res Dev. 2000 Nov-Dec;37(6):701-8.
- Colombo G, Joerg M, Schreier R, Dietz V. Treadmill training of paraplegic patients using a robotic orthosis. J Rehabil Res Dev. 2000 Nov-Dec;37(6):693-700.
- Hornby TG, Zemon DH, Campbell D. Robotic-assisted, body-weight-supported treadmill training in individuals following motor incomplete spinal cord injury. Phys Ther. 2005 Jan;85(1):52-66.
- Trimble MH, Behrman AL, Flynn SM, Thigpen MT, Thompson FJ. Acute effects of locomotor training on overground walking speed and H-reflex modulation in individuals with incomplete spinal cord injury. J Spinal Cord Med. 2001 Summer;24(2):74-80. doi: 10.1080/10790268.2001.11753558.
- Day KV, Kautz SA, Wu SS, Suter SP, Behrman AL. Foot placement variability as a walking balance mechanism post-spinal cord injury. Clin Biomech (Bristol, Avon). 2012 Feb;27(2):145-50. doi: 10.1016/j.clinbiomech.2011.09.001. Epub 2011 Oct 14.
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia
Primární dokončení (Aktuální)
Dokončení studie (Aktuální)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Odhad)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
Další identifikační čísla studie
- B4024-I
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
produkt vyrobený a vyvážený z USA
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .
Klinické studie na Poranění míchy
-
Assiut UniversityDokončeno
-
University of Sao PauloZatím nenabírámeOtok | Varixy; CordBrazílie
-
Qianfoshan HospitalChinese Medical AssociationNábor
-
Tel-Aviv Sourasky Medical CenterNeznámýOprava kraniosynostózy | Untethering of Cord
-
M.D. Anderson Cancer CenterNational Cancer Institute (NCI)NáborTransplantace hematopoetických kmenových buněk | Transplantace kmenových buněk z pupečníkové krve | Transplantace pupečníkové krveSpojené státy
-
National University of MalaysiaMalaysia Automotive Robotics and Innovation of Technology InstituteDokončenoProtilátka | Vakcína | Mateřský | CordMalajsie
-
University of Southern CaliforniaDokončenoDysfonie | Atrofie hlasivek | Presbylarynx | Atrofie; Hrtan | Presbylarynges | Jizva vokálních záhybů | Sulcus Vocalis z Vocal CordSpojené státy