The MetroHealth System

Therapies for Recovery of Hand Function After Stroke

Purpose

After a stroke, it is very common to lose the ability to open the affected hand. The purpose of this study is to compare the effects of three different therapies on recovery of hand function after stroke and determine if any one is better than the other.

Conditions

Stroke
Upper Extremity Paresis
Hemiplegia

Eligibility

Eligible Ages: Between 21 Years and 90 Years
Eligible Genders: All
Accepts Healthy Volunteers: No

Inclusion Criteria

6 to 24 months since a first clinical cortical or subcortical, hemorrhagic or nonhemorrhagic stroke - unilateral upper limb hemiparesis with finger extensor strength of grade no more than 4 out of 5 on the Medical Research Council (MRC) scale - score of at least 1 and no more than 11 out of 14 on the hand section of the upper extremity Fugl-Meyer Assessment - adequate active movement of the shoulder and elbow to position the hand in the workspace for table-top task practice (necessary for the lab task practice sessions) - able to follow 3-stage commands - able to recall at least 2 of a list of 3 items after 30 minutes - skin intact on the hemiparetic arm - surface stimulation of the paretic finger and thumb extensors produces functional hand opening without pain (this will exclude those who have too much flexor spasticity) - able to hear and respond to cues from stimulator - not receiving occupational therapy (no concomitant OT) - full voluntary opening/closing of the contralateral (less affected) hand - demonstrates ability to follow instructions for operating the stimulator or have a caregiver who will assist them

Exclusion Criteria

co-existing neurologic diagnosis of peripheral nerve injury, Parkinson's disease, spinal cord injury, traumatic brain injury, or multiple sclerosis - uncontrolled seizure disorder - brainstem stroke - uncompensated hemineglect - severe shoulder or hand pain - insensate forearm or hand - history of potentially fatal cardiac arrhythmias with hemodynamic instability - implanted electronic systems (e.g. pacemaker) - botulinum toxin injections to any upper extremity muscle within 3 months of enrolling - pregnant women due to unknown risks of surface NMES during pregnancy - lack of functional passive range of motion of the wrist or fingers of affected side - diagnosis (apart from stroke) that substantially affects paretic arm and hand function - deficits in communication that interfere with reasonable study participation - lacking sufficient visual acuity to see the stimulator's display - concurrent enrollment in another investigational study

Study Design

Phase: N/A
Study Type: Interventional
Allocation: Randomized
Intervention Model: Parallel Assignment
Primary Purpose: Treatment
Masking: Single (Outcomes Assessor)

Arm Groups

Arm	Description	Assigned Intervention
Experimental CCFES	Contralaterally Controlled Functional Electrical Stimulation (CCFES) uses an electrical stimulator and surface electrodes placed over the paretic finger and thumb extensors to deliver stimulation with an intensity that is proportional to the degree of opening of the contralateral unimpaired hand wearing an instrumented glove. Thus, volitional opening of the nonparetic hand produces stimulated opening of the paretic hand. During the lab visits, participants in the CCFES group will use CCFES to assist hand opening during occupational therapy task practice. During their home sessions, participants in the CCFES group will use CCFES to perform hand opening exercise.	Device: Electrical Stimulator An electrical stimulator will be used to deliver electrical current through surface electrodes to produce hand opening by making the paretic finger and thumb extensor muscles contract. The stimulator can be programmed to turn on and off in a repetitive cyclic fashion (i.e., cNMES) or be programmed to deliver stimulation with an intensity that corresponds to the opening of a glove instrumented with sensors and plugged into the stimulator (i.e., CCFES). Behavioral: Occupational Therapy Task practice that requires movement and use of the paretic hand under the guidance of a trained therapist.
Active Comparator cNMES	Cyclic Neuromuscular Electrical Stimulation (cNMES) uses an electrical stimulator and surface electrodes over the paretic finger and thumb extensors to deliver electrical stimulation to open the weak hand. The stimulation automatically turns on and off causing the weak hand to open repetitively for several seconds at a time. During the lab visits, participants in the cNMES group will receive occupational therapy task practice. During their home sessions, participants in the cNMES group will use cNMES to perform hand opening exercise.	Device: Electrical Stimulator An electrical stimulator will be used to deliver electrical current through surface electrodes to produce hand opening by making the paretic finger and thumb extensor muscles contract. The stimulator can be programmed to turn on and off in a repetitive cyclic fashion (i.e., cNMES) or be programmed to deliver stimulation with an intensity that corresponds to the opening of a glove instrumented with sensors and plugged into the stimulator (i.e., CCFES). Behavioral: Occupational Therapy Task practice that requires movement and use of the paretic hand under the guidance of a trained therapist.
Active Comparator Task Oriented Therapy	Task Oriented Therapy (TOT) focuses on practicing using the weak hand to practice activities of daily living tasks. During the clinic visits, participants in the TOT group will receive occupational therapy task practice. During their home sessions, participants in the TOT group will practice using their hand to complete a list of tasks given to them by the therapist to ensure that the participant receives a high dose of task practice.	Behavioral: Occupational Therapy Task practice that requires movement and use of the paretic hand under the guidance of a trained therapist.

More Details

Status: Active, not recruiting
Sponsor: MetroHealth Medical Center

Study Contact

Detailed Description

A single-blinded randomized controlled trial will be carried out to assess and compare the effects of 12 weeks of Contralaterally Controlled Functional Electrical Stimulation (CCFES), Cyclic Neuromuscular Electrical Stimulation (cNMES), and Task Oriented Training. Dexterity, upper limb impairment, and activity limitation will be assessed at 0 (baseline), 12 (end of treatment), and 36 weeks. The treatment dose will be the same for all three groups: 10 sessions per week of self-administered treatment at home plus 2 sessions per week of group-specific occupational therapy in the lab.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.