Improving Stroke Motor Control With Non-invasive Brain Stimulation and Functional Electrical Stimulation

Not Applicable

Recruiting

• Conditions: Hand; Stroke; Rehabilitation
• Interventions: Device: transcranial direct current stimulation and electrical stimulator

• Registration Number: NCT03857529
• Lead Sponsor: MetroHealth Medical Center

Brief Summary

This pilot study for stroke patients with chronic upper limb hemiplegia will examine the effects of non-invasive brain stimulation and neuromuscular electrical stimulation on hand motor control and corticospinal excitability. Specifically, this study will investigate the effects of timing and delivery of tDCS in conjunction with contralaterally controlled functional electrical stimulation.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2019-02-26
• Study First Submitted QC: 2019-02-26
• Study First Posted: 2019-02-28
• Study Start: 2019-08-01
• Status Verified: 2024-08
• Last Update Submitted: 2024-08-28
• Last Update Posted: 2024-08-29
• Primary Completion: 2026-08-01
• Study Completion: 2026-08-01

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 15

Inclusion Criteria

1. Age ≥ 21

2. ≥ 6 months since first clinical hemorrhagic or nonhemorrhagic stroke

3. Able to follow 3-stage commands and remember 2 of 3 items after 30 minutes

4. Full volitional elbow extension/flexion and hand opening/closing of unaffected limb

5. Adequate active movement of shoulder and elbow to position the paretic hand in the workspace for table-top task practice

6. Patient must be able to sit unassisted in an armless straight-back chair for the duration of the screening portion of the eligibility assessment

7. Medically stable

8. ≥ 10° finger extension

9. Unilateral upper limb hemiparesis with finger extensor strength of ≤ grade 4/5 on the manual muscle test AND a score of

   ≥1 and ≤ 11/14 on the hand section of the upper extremity Fugl-Meyer Assessment

10. Skin intact on hemiparetic arm, hand and scalp

11. While relaxed, surface neuromuscular electrical stimulation of finger extensors and thumb extensors and/or abductors produces a functional degree of hand opening without pain.

12. No significant visual or hearing impairment

Exclusion Criteria

1. Co-existing neurological condition other than prior stroke involving the hemiparetic upper limb (e.g., peripheral nerve injury, Parkinson's disease, spinal cord injury, traumatic brain injury, multiple sclerosis).
2. Uncontrolled seizure disorder
3. Use of seizure lowering threshold medications at the discretion of the study physician (Dr. Rich Wilson)
4. Cardiac pacemaker or other implanted electronic device and/or stent
5. Pregnant
6. Intramuscular botox injections in any upper extremity muscle in the last 3 months
7. Insensate arm, forearm, or hand
8. Severely impaired cognition and communication
9. Uncompensated hemi-neglect (extinguishing to double simultaneous stimulation)
10. Severe shoulder or hand pain (unable to position hand in the workspace without pain)
11. Metal implant in the head

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
unconventional tDCS concurrent with CCFES	transcranial direct current stimulation and electrical stimulator	tDCS cathode placed over the lesioned hemisphere and anode placed over the non-lesioned hemisphere
conventional tDCS concurrent with CCFES	transcranial direct current stimulation and electrical stimulator	tDCS anode placed over the lesioned hemisphere and cathode placed over the non-lesioned hemisphere
conventional tDCS preceding CCFES	transcranial direct current stimulation and electrical stimulator	tDCS anode placed over the lesioned hemisphere and cathode placed over the non-lesioned hemisphere
unconventional tDCS preceding CCFES	transcranial direct current stimulation and electrical stimulator	tDCS cathode placed over the lesioned hemisphere and anode placed over the non-lesioned hemisphere
sham tDCS with CCFES	transcranial direct current stimulation and electrical stimulator	sham tDCS preceding and concurrent with CCFES

Primary Outcome Measures

Name	Time	Method
Corticospinal Excitability	up to one hour post intervention	Change in corticospinal excitability will be measured with transcranial magnetic stimulation
Reaction Time	up to one hour post intervention	Change in reaction time will be assessed with visual and auditory cues.

Trial Locations

Locations (1)

MetroHealth Medical Center; 🇺🇸 Cleveland, Ohio, United States