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Upper Arm Reahabilitation After Stroke and Video Game

Effect of Early Upper Arm Rehabilitation After Stroke Using Adaptative Video Games

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01554449
Acronym
MARGAUT
Enrollment
62
Registered
2012-03-15
Start date
2011-09-12
Completion date
2016-07-12
Last updated
2018-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebro-vascular Accident, Grasping, Reaching, Stroke, Upper Arm Disability

Keywords

Stroke, Upper arm, Rehabilitation, Motor function, Video games, Virtual reality, Occupational Therapy, Functional MRI

Brief summary

The purpose of this study is to assess the efficiency of occupational therapy enhanced by dedicated adaptative video games in rehabilitation of the upper arm of stroke patients in the acute phase after their cerebro-vascular accident. Our hypothesis is that occupational therapy enhanced by dedicated adaptative video games is more efficient in improving motor recovery of the upper arm than conventional occupational therapy alone.

Detailed description

Introduction : Stroke constitutes one of the most disabiliting desease in industrialized countries, leading to major deficiencies, especially in the upper arm (concerning 50 to 80% of post-stroke patients). Upper arm rehabilitation after stroke improved during the last ten years, with the development of new rehabilitation methods including constraint induced therapy, mirror therapy, mental imaging, virtual reality and robotics. Video games and virtual reality are very promising in this field, and the development of new adaptative games dedicated to upper arm rehabilitation after stroke is necessary to enhance the benefit of those devices in therms of sensori-motor and functional recovery. Objectives: To prove the efficiency of video-gaming (using dedicated adaptative games) on recovery of motor function of the upper armafter stroke, compared to a conventional rehabilitation program. Design: Multicentric Randomized Controlled TrialParticipants: 50 early stroke patients and 12 healthy control persons will be included in this trial. Inclusion criteria for patients are as follow: age\>18, onset of stroke \<6 weeks, first unique supra-tentorial ischemic or haemorrhagic stroke, Fugl Meyer score of the upper arm \< 30/66 at inclusion. Exclusion criteria are as follow: severe neglect or aphasia, upper arm severe orthopedic limitation, shoulder pain \> 5/10, contra-indication to MRI. Methods:All patient will get a standard program of rehabilitation 5 days/week duiong six weeks, including physiotherapy (one or two sessions/day), occupational therapy (one session/day) and speech therapy if necessary (one session/day). Patients will be randomized in two groups: the treated group receiving an additional session of 30 to 45 minutes of daily rehabilitation with video games under the supervision of an occupational therapist, and the control group receiving the same anount of standard rehabilitation provided by an occupational therapist.Assesment will be conducted at inclusion (J0), at the end of the program (Week 6: W6) and at follow-up (end of month 6: M6)). Recorded datas: The primary endpoint is the difference in increasing the upper arm Fugl Meyer Score (FMS) between both groups at W6. Secondary criterions include: FMS at M6, Box and Block Test at W6 and M6, Nine Hole Peg test at W6 and M6, Wolf Motor Function Test at W6 and M6, Motor Activity Log at W6 and M6, Barthel Index at W6 and M6, SF-36 at W6 and M6. Functional MRI and tensor diffusion imaging will also be conducted in 25 patients and 12 controls, at J0 and W6. Evolution of cerebral plasticity and correlations between cerebral re-organisations and kinematic characteristics of upper arm movements will be provided.

Interventions

PROCEDUREserious game reeducation

It's a daily session (45 minutes) of reeducation by serious game (kinect) compared to a daily session (45 minutes) of conventional reeducation

PROCEDUREfunctional MRI

the functional MRI (siemens) will be done on 25 stroke patients and 12 healthy volunteers at baseline and at 6 weeks.

Sponsors

University Hospital, Montpellier
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* age \> 18 * onset of stroke \< 6 weeks * first unique supra-tentorial ischemic or haemorhagic stroke * Fugl Meyer score of the upper arm \< 30/66 at baseline

Exclusion criteria

* severe neglect or aphasia * upper arm severe orthopedic limitation * shoulder pain \> 5/10 * pregnancy \< 3 months * Contraindication to MRI

Design outcomes

Primary

MeasureTime frameDescription
Efficacy assessment of the serious game on the recovery of the upper limbat 6 weeksDifference in increase of the Upper Arm Fugl Meyer Score (max: 66) between both groups, at the end of the rehabilitation program (week 6)

Secondary

MeasureTime frameDescription
Box and Block Test assessment between both groupsat 6 Weeks and 6 MonthsThe box and block test assess the global capacities of prehension of patients. It's important to compare these capacities between both groups of treatment.
Wolf Motor Function Test assessment between both groups.at 6 weeks and at 6 monthsTo assess the motor capacity by the Wolf motor funtion at 6 Weeks and after 6 Months.
Motor Activity Log assessment between both groupsat 6 weeks and at 6 monthsThis test assess the frequency of use and the quality of the movement.
Fugl Meyer Score between both groupsat 6 MonthsDifference in increase of the Upper Arm Fugl Meyer Score (max: 66) between both groups, at the end of the study(6 months)
Functional MRI Assessment between controls and patientsat baseline and at 6 weeksFunctional MRI permits to study of the topographics neuronal circuits involved in the recovery of the motor functions of the upper limb: evaluation of the profiles of activation involved in the execution of the movement of fingers flexion / extension involving the right hemisphere and then the left hemisphere.
Nine Hole Peg test assessment between both groupsat 6 weeks and at 6 monthsTo assess the efficacy of Serious Game on manual dexterity on the duration of Nine Hole Peg test.
tensor diffusion analysis between controls and patientsat 6 weeksThe tensor diffusion imaging will also be conducted in 25 patients and 12 controls, at baseline and at 6 weeks. Evolution of cerebral plasticity and correlations between cerebral re-organisations and kinematic characteristics of upper arm movements will be provided.
Barthel Index and SF-36at 6 weeks and at 6 monthsThe Barthel Index assess the global functional capacities by a score (calculated /100)between both groups of patients. The SF-36 is a self-questionnaire which permits the evalulation of quality of life.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026