Clinical Trials Directory

Trials / Unknown

UnknownNCT03555838

Combined Robotic Training and tDCS in Chronic SCI

Improving Hand Function in Chronic SCI With Combined Robotic Training and tDCS

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
13 (actual)
Sponsor
Burke Medical Research Institute · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to establish the value of combined non-invasive stimulation (tDCS) and behavioral training (robotics) in SCI rehabilitation, and understand the mechanisms of this interaction and its relationship to functional outcome. The investigators hypothesize that supplementary tDCS will augment the functional improvement from robot-training, in chronic SCI.

Detailed description

Study design: Using a within-subjects repeated measures design, up to 40 SCI participants will be randomized to receive 6-week hand robotic training preceded by 20 min anodal 2mA tDCS or sham (3 sessions/week, 18 sessions total). Clinical and functional scales, robotic kinematics and neurophysiological data (TMS evaluation) will be collected before and after the combined intervention period, and a month later (pre, post and follow up evaluations). Randomization will be done using a randomized block design with a block size of 2. All participants, raters, and experimenters will be blinded to treatment allocation. AIM 1. To determine whether combining non-invasive brain stimulation (tDCS) and behavioral training (robotics) in SCI can lead to functional improvement. The investigators hypothesize that the group receiving the real stimulation will obtain a greater clinical improvement in hand motor function. Using a within subjects repeated measures design, baseline clinical hand function (Box and Blocks test) will be compared to post 6-week robotic training intervention, and then a month later (follow up), each session preceded by real (2mA anodal M1) or sham tDCS. AIM 2. To examine the kinematic changes (from robotic measures) associated with the combined training. Quantitative measurements obtained from robotics are highly sensitive, precise and reliable. The investigators predict an enhancement of motor performance in all participants, measured by 5 key parameters: mean speed, peak speed, smoothness, aim and deviation; with greater improvements in the intervention group receiving the pre-conditioning effect of transcranial stimulation. These data will identify features of motor control that underlie improvements in clinical function, when comparing the two intervention groups. AIM 3. To identify and compare the neurophysiological mechanisms (by TMS) associated with the combined training. The relationship between clinical improvement in neurophysiological measures pertaining to robotic motor training alone and combined with tDCS will be assessed. Measuring changes in MEP amplitude of hand muscles before and after the training will establish a) the plasticity associated with training alone and with supplementary brain stimulation, b) the neurophysiological characteristics of patients who respond better to the training. By understanding how brain excitability changes underpin motor dysfunction, and motor recovery, interventions can be more effectively prescribed and prognoses established.

Conditions

Interventions

TypeNameDescription
OTHERtranscranial direct current stimulationTranscranial direct current stimulation, a form of neuromodulation that uses a low direct current delivered via sponge electrodes on the head.
OTHERsham transcranial direct current stimulationan inactive or placebo version of transcranial direct current stimulation placed on the head via sponge electrodes.

Timeline

Start date
2017-05-01
Primary completion
2019-01-01
Completion
2023-12-01
First posted
2018-06-14
Last updated
2022-03-02

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03555838. Inclusion in this directory is not an endorsement.