BurtVision™ for Arm Rehabilitation in Chronic Stroke Survivors:

Sponsor
Spaulding Rehabilitation Hospital
Study ID
NCT04940403
Status
Not Yet Recruiting

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Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 80 Years
Healthy Volunteers
Not accepted

Interventions

  • Burt — DEVICE
    18 one-hour sessions of unimanual upper-limb tasks during robot-assisted training with the Burt.
  • Burt + BurtVision — DEVICE
    18 one-hour sessions of combination of unimanual and bimanual upper-limb tasks during robot-assisted training with the BurtVision.

Study Details

The focus of this study is to perform a preliminary assessment of the efficacy of the BurtVision system. While the Burt robotic-arm assists the patient's upper-limb in their movements, BurtVision will allow the patient to perform unimanual and bimanual activities while leveraging augmented reality games. The investigators will compare clinical outcomes when the BurtVisions ystem is used for training solely relying on unimanual tasks vs. when it is used for training relying on both unimanual and bimanual tasks.

Key Dates

First listed
Jun 25, 2021
Start date
Sep 1, 2026
Status verified
Mar 2026
Primary completion
Feb 15, 2027
Completion
Jun 1, 2027

Study Design

Enrollment
38 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Active Comparator: Unimanual robot-assisted upper-limb rehabilitation
    Participants randomized to this arm of the study will undergo 18 one-hour sessions of robot-assisted upper-limb rehabilitation. During the sessions, study participants will only train their hemiparetic arm (unimanual tasks only).
  • Experimental: Bimanual robot-assisted upper-limb rehabilitation
    Participants randomized to this arm of the study will undergo 18 one-hour sessions of robot-assisted upper-limb rehabilitation. During the sessions, study participants will train their hemiparetic arm as well as interacting with the contralateral arm for bimanual tasks (unimanual + bimanual tasks).

Primary Outcome Measure

Motor Activity Log- Amount of Use [ Time Frame: Data will be collected at baseline and at 7-8 weeks ]

Central Contacts

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