Optimizing Transcranial Direct Current Stimulation for Motor Recovery From Hemiparesis

Stroke Clinical Trial

Official title:

Optimizing Transcranial Direct Current Stimulation for Motor Recovery From Severe Post-stroke Hemiparesis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03124147
• Other study ID #: 11CRP7220009
• Status: Completed
• Phase: N/A
• First received: April 18, 2017
• Last updated: April 21, 2017
• Start date: August 2011
• Est. completion date: October 2013

Study information

• Verified date: April 2017
• Source: University of Kentucky
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will compare the effectiveness of different polarities of transcranial direct current stimulation paired with intensive motor training in recovery of upper extremity function in individuals with severe post-stroke hemiparesis. The hypothesis is that more severely impaired individuals will derive greater benefit from anodal stimulation of the ipsilesional hemisphere or cathodal stimulation of the contralesional hemisphere than dual stimulation (anodal applied to the ipsilesional hemisphere and cathodal applied to the contralesional hemisphere.)

Description:

This study has 2 aims: 1) determine which transcranial direct current stimulation (tDCS) electrode configuration is most effective in combination with motor training to promote motor recovery from severe post-stroke hemiparesis; and 2) begin to clarify the extent to which baseline transcranial magnetic stimulation (TMS) measures predict response to tDCS, as well as the effects of tDCS paired with motor training on TMS measures of motor cortical organization.

To accomplish these aims, the investigators will recruit 36 human subjects with severe post-stroke hemiparesis and assign each subject to 1 of 4 tDCS conditions (anodal excitatory ipsilesional; cathodal inhibitory contralesional; a combination of anodal excitatory ipsilesional during cathodal inhibitory contralesional; or sham). Each subject will undergo a 20-minute stimulation session once a day for 10 days over a 2-week period. Each session will be followed by 3 hours of intensive, task-oriented upper extremity motor training.

Outcome measures for this study include TMS motor cortical maps and standardized tests of motor performance. The investigators hypothesize that all groups will show improvement in all measures; however, both the anodal excitatory ipsilesional group and the cathodal inhibitory contralesional group will show significantly greater improvement compared with the other 2 groups. The investigators will also find evidence clarifying whether the presence or absence of motor-evoked potentials (MEPs) has predictive value regarding which tDCS configuration would be most effective for a particular subject.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 38
• Est. completion date: October 2013
• Est. primary completion date: October 2013
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Chronic stroke patients

• Single stroke

• Chronic (more than 12 months after from stroke)

• At least 18 years old, but there is no upper age range for this project.

• Participants NOT able to extend the affected metacarpophalangeal joints at least 10° and the wrist 20°.

Exclusion Criteria:

• History of head injury with loss of consciousness, seizure, severe alcohol or drug abuse, psychiatric illness

• Within 3 months of recruitment, use of drugs known to exert detrimental effects on motor recovery

• Cognitive deficit severe enough to preclude informed consent

• Positive pregnancy test or being of childbearing age and not using appropriate contraception

• Participants with history of untreated depression.

Related Conditions & MeSH terms

• Cerebrovascular Accident
• Paresis
• Stroke

Intervention

Device:
• Neuroconn Eldith stimulator by Magstim
Transcranial direct current stimulation to the ipsilesional hemisphere, contralesional hemisphere, or both, paired with task-oriented therapy.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Lumy Sawaki

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Fugl Meyer Assessment		Score change after 10 days of intervention compared to baseline; Score change after 1-month after the intervention compared to baseline
Secondary	Change in Action Research Arm Test		Score change after 10 days of intervention compared to baseline; Score change after 1-month after the intervention compared to baseline
Secondary	Change in Stroke Impact Scale		Score change after 10 days of intervention compared to baseline; Score change after 1-month after the intervention compared to baseline