Driving Neuroplasticity With Nerve Stimulation and Modified CIT

Stroke Clinical Trial

Official title:

Driving Neuroplasticity With Nerve Stimulation and Modified Constraint-Induced Therapy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02587234
• Other study ID #: R03HD049408
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: November 2006
• Est. completion date: April 2012

Study information

• Verified date: September 2023
• Source: University of Kentucky
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The investigators proposed to evaluate the effectiveness of sustained peripheral nerve stimulation (PNS) to enhance the therapeutic effects of a modified form CIT (mCIT).

Description:

Stroke is one the most devastating and prevalent diseases, but efforts to limit the amount of tissue damaged in the acute phase have been disappointing, highlighting the need for effective therapeutic interventions after neurologic damage has occurred. A major goal of the research in stroke rehabilitation is to harness the capacity of the brain to reorganize after neurologic damage has occurred and thus ultimately lead to successful recovery of function. Data from animal and human models have suggested that sensory input plays an important role in motor output, possibly by influencing cortical plasticity. However, in spite of the advances to date, little is known about the extent to which sensory input in the form of peripheral nerve stimulation can be successfully combined to physical training. A new emerging approach called constraint-induced therapy (CIT) is an intensive functional motor training and has produced promising results in the field of stroke rehabilitation. CIT involves restraining the unaffected arm with a sling or glove combined with intense task-oriented therapy of the affected side for six hours daily during 2 weeks. This pilot study will evaluate the effectiveness of sustained peripheral nerve stimulation coupled with functional motor training to improve hand motor function. While the functional motor training follows identical principles of CIT, the length of daily training will be shortened to 4 hours daily and thus the investigators will refer in this proposal as a modified CIT. Preliminary data for this study demonstrated that peripheral nerve stimulation results in increased cortical motor excitability in normal subjects. In addition, learning and use-dependent plasticity can be substantially enhanced by a single session of 2 hours of peripheral nerve stimulation in chronic stroke patients. The goal of this study is to test the hypothesis that stroke patients treated with upper extremity peripheral nerve stimulation preceding CIT (intervention group) will have improved hand motor function compared to a group receiving lower extremity peripheral nerve stimulation and CIT (control group).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 21
• Est. completion date: April 2012
• Est. primary completion date: February 2010
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years and older

Eligibility

Inclusion Criteria:

• Chronic stroke patients

• Single stroke

• Chronic (more than 12 months after from stroke)

• At least 21 years old, but there is no upper age range for this project.

• Participants must be able to extend the affected metacarpophalangeal joints at least 10° and the wrist 20°.

Exclusion Criteria:

• History of carpal tunnel syndrome and conditions that commonly cause peripheral neuropathy, including diabetes, uremia, or associated nutritional deficiencies

• History of head injury with loss of consciousness, 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
• Stroke

Intervention

Device:
• peripheral nerve stimulation
Non-invasive stimulation of median, ulnar and radial nerves

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
University of Kentucky

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Wolf Motor Function Test (WMFT), Timed Portion	Score at post-intervention minus score at baseline, score at 1-month follow-up minus score at baseline	baseline, post-intervention, 1-month follow-up
Secondary	Change in Fugl Meyer Assessment Motor Score	Score at post-intervention minus score at baseline, score at 1-month follow-up minus score at baseline. The scores can range from 0 to 66, with higher scores indicating better performance. The scores are calculated by summing the scores to the 33 individual tasks.	baseline, post-intervention, 1-month follow-up
Secondary	Change in Action Research Arm Test (ARAT)	Values given are score at post-intervention minus score at baseline, score at 1-month follow-up minus score at baseline.; The ARAT's is a 19 item measure divided into 4 sub-tests (grasp, grip, pinch, and gross arm movement).; Performance on each item is rated on a 4-point ordinal scale ranging from: 3: Performs test normally 2: Completes test, but takes abnormally long or has great difficulty; 1: Performs test partially 0: Can perform no part of test The maximum score on the ARTS is 57 points (possible range 0 to 57).	baseline, post-intervention, 1-month follow-up