search
Back to results

PCMS Task After Moderate-to-severe Stroke

Primary Purpose

Stroke

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Task-specific PCMS
Task-specific sham-PCMS
PCMS-rest
Sponsored by
Amit Sethi
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring Stroke, Hand, Brain stimulation

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age between 18-80 years Diagnosis of first-ever subcortical stroke (single cerebrovascular accident) Stroke onset of at least six months prior to the time of participation A score of at least 1 out of 2 on the spherical grasping item of the Fugl-Meyer Upper Extremity Subscale to allow participants to grasp the ball Cognitive skills to actively participate, as indicated by scores of > 23 on the Mini-Mental Status Examination English speaking Exclusion Criteria: Inability to elicit a motor evoked potential (MEP) in the EDC muscle even with a 20% background muscle contraction Presence of severe aphasia Excessive spasticity of the wrist and finger muscles, defined as a Modified Ashworth Score >2 Diagnosis of neurological disorders other than stroke History of seizure or epilepsy Orthopedic/musculoskeletal conditions (e.g., arthritis) affecting the upper extremity Presence of metallic implants in the head or neck Currently or planning to become pregnant Difficulty maintaining alertness or remaining still Ferromagnetic metallic implants, pacemakers, other implanted devices, or ventilators for magnetic resonance imaging (MRI) Bodyweight > 300 lbs due to MRI scanner dimensions (for subjects also undergoing MRI) Psychiatric diagnosis according to the criteria of the Diagnostic and Statistical Manual of Mental Disorder, Fifth Edition (DSM-V), or who are on psychotropic medication Life expectancy less than the duration of the study Excessive pain in the paretic hand, defined as a Visual Analog Scale Score >4 Participation in concurrent occupational therapy Current use of recreational drugs and stimulants like cocaine and methylenedioxymethamphetamine (MDMA)

Sites / Locations

  • Neuromotor Recovery and Rehabilitation LabRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Arm Label

Task-specific PCMS, PCMS-rest, Task-specific sham-PCMS

Task-specific PCMS, Task-specific sham-PCMS, PCMS-rest

PCMS-rest, Task-specific PCMS, Task-specific sham-PCMS

PCMS-rest, Task-specific sham-PCMS, Task-specific PCMS

Task-specific sham-PCMS, Task-specific PCMS, PCMS-rest

Task-specific sham-PCMS, PCMS-rest, Task-specific PCMS

Arm Description

During Task-specific paired corticospinal-motor neuronal stimulation (PCMS) participants will receive PCMS [Transcranial Magnetic Stimulation (TMS) + Peripheral Nerve Stimulation (PNS)] with task-specific practice. During PCMS rest participants will receive PCMS (TMS + PNS) without task-specific practice. During Task-specific sham-PCMS participants will receive task-specific practice with sham PCMS (TMS + PNS).

During Task-specific PCMS participants will receive PCMS (TMS + PNS) with task-specific practice. During PCMS rest participants will receive PCMS (TMS + PNS) without task-specific practice. During Task-specific sham-PCMS participants will receive task-specific practice with sham PCMS (TMS + PNS).

During Task-specific PCMS participants will receive PCMS (TMS + PNS) with task-specific practice. During PCMS rest participants will receive PCMS (TMS + PNS) without task-specific practice. During Task-specific sham-PCMS participants will receive task-specific practice with sham PCMS (TMS + PNS).

During Task-specific PCMS participants will receive PCMS (TMS + PNS) with task-specific practice. During PCMS rest participants will receive PCMS (TMS + PNS) without task-specific practice. During Task-specific sham-PCMS participants will receive task-specific practice with sham PCMS (TMS + PNS).

During Task-specific PCMS participants will receive PCMS (TMS + PNS) with task-specific practice. During PCMS rest participants will receive PCMS (TMS + PNS) without task-specific practice. During Task-specific sham-PCMS participants will receive task-specific practice with sham PCMS (TMS + PNS).

During Task-specific PCMS participants will receive PCMS (TMS + PNS) with task-specific practice. During PCMS rest participants will receive PCMS (TMS + PNS) without task-specific practice. During Task-specific sham-PCMS participants will receive task-specific practice with sham PCMS (TMS + PNS).

Outcomes

Primary Outcome Measures

Transcranial magnetic stimulation to evaluate corticospinal transmission
Corticospinal transmission will be assessed by examining the percent change of the peak-to-peak motor evoked potential (MEP) amplitude relative to baseline.

Secondary Outcome Measures

Voluntary force production to evaluate motor performance
We will measure force production of the wrist and finger extensors (EDC) to evaluate motor performance using load cells embedded in cushioned customized platforms. Participants will perform isometric wrist and finger extension movements against load cells. We will calculate the percent change of maximum force output.
Maximum finger excursions to evaluate motor performance
Three-dimensional biomechanical data will be collected to evaluate motor performance using a motion capture system. Reflective markers will be placed on the participant's paretic forearm, hand, and fingers to track wrist and finger movements during a maximum hand opening task. Hand biomechanics will be evaluated by computing the percent change of maximum finger excursions during the hand opening task.
Maximum finger spread to evaluate motor performance
Three-dimensional biomechanical data will be collected to evaluate motor performance using a motion capture system. Reflective markers will be placed on the participant's paretic forearm, hand, and fingers to track wrist and finger movements during a maximum hand opening task. Hand biomechanics will be evaluated by computing the percent change of maximum finger spread during the hand opening task.
Box and Block Test
The Box and Block Test (BBT) measures unilateral gross manual dexterity and the ability to release objects. We will calculate the percent change of the total number of blocks transferred in one minute.

Full Information

First Posted
February 10, 2023
Last Updated
September 8, 2023
Sponsor
Amit Sethi
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
search

1. Study Identification

Unique Protocol Identification Number
NCT05736653
Brief Title
PCMS Task After Moderate-to-severe Stroke
Official Title
Strengthening Task Specific Activation of Paretic Hand Muscles After moderate-to- Severe Chronic Stroke
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 29, 2023 (Actual)
Primary Completion Date
January 30, 2026 (Anticipated)
Study Completion Date
January 30, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Amit Sethi
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Researchers at the University of Pittsburgh are conducting a research study to see how combining brain, nerve, and hand stimulation affect hand movement after stroke. The primary purpose of this study is to examine changes in the connection between the brain and the weak hand muscles after the combined brain, nerve, and hand stimulation. The primary hypothesis is that the combined brain, nerve, and hand stimulation will increase the the connection between the brain and the weak hand muscles. The secondary purpose of this study is to examine changes in weak hand's movement and function after the combined brain, nerve, and hand stimulation. The secondary hypothesis is that the combined brain, nerve, and hand stimulation will increase weak hand movement and function.
Detailed Description
A total of 40 participants will be enrolled in this study. During the intervention sessions, Participants will receive three combinations of the brain, hand, and nerve stimulations. Each participant will complete three intervention sessions for the short-term effect of the intervention. The time between sessions is 3-7 days. After data collection is completed for the short-term effect part of the study, 5 out of 40 participants will be randomly chosen to enroll in the long-term effect part of the intervention. Those participants will take part in 18 intervention sessions. The sessions will be administered three times a week for six weeks. In the short-term effect part of the study, participants will complete the following three sessions: Repeated brain, hand, and nerve stimulations while practicing a task. In this session, participants will receive 120 pairs of brain, hand, and nerve stimulation while repeatedly grasp and release a ball with the weak hand. The hand stimulation will help participants to release the ball. Repeated brain and nerve stimulations during rest. In this session, participants will receive 120 pairs of brain and nerve stimulation while the weak hand is resting (or not performing a task). Hand stimulation while practicing a task. In this session, participants will practice grasping and releasing the task 120 times with hand stimulation. The hand stimulation will help participants to release the ball. In the long-term effect part of the study, participants will complete the following session (3/week for 6 weeks): During the intervention, participants will receive repeated brain, hand, and nerve stimulations while practicing a task. They will receive 120 pairs of brain, hand, and nerve stimulation while repeatedly grasp and release a ball with the weak hand. The hand stimulation will help participants to release the ball. We will give rest breaks during the practice of the task.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
Stroke, Hand, Brain stimulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
We will employ a single group pre-post design.
Masking
Participant
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Task-specific PCMS, PCMS-rest, Task-specific sham-PCMS
Arm Type
Experimental
Arm Description
During Task-specific paired corticospinal-motor neuronal stimulation (PCMS) participants will receive PCMS [Transcranial Magnetic Stimulation (TMS) + Peripheral Nerve Stimulation (PNS)] with task-specific practice. During PCMS rest participants will receive PCMS (TMS + PNS) without task-specific practice. During Task-specific sham-PCMS participants will receive task-specific practice with sham PCMS (TMS + PNS).
Arm Title
Task-specific PCMS, Task-specific sham-PCMS, PCMS-rest
Arm Type
Experimental
Arm Description
During Task-specific PCMS participants will receive PCMS (TMS + PNS) with task-specific practice. During PCMS rest participants will receive PCMS (TMS + PNS) without task-specific practice. During Task-specific sham-PCMS participants will receive task-specific practice with sham PCMS (TMS + PNS).
Arm Title
PCMS-rest, Task-specific PCMS, Task-specific sham-PCMS
Arm Type
Experimental
Arm Description
During Task-specific PCMS participants will receive PCMS (TMS + PNS) with task-specific practice. During PCMS rest participants will receive PCMS (TMS + PNS) without task-specific practice. During Task-specific sham-PCMS participants will receive task-specific practice with sham PCMS (TMS + PNS).
Arm Title
PCMS-rest, Task-specific sham-PCMS, Task-specific PCMS
Arm Type
Experimental
Arm Description
During Task-specific PCMS participants will receive PCMS (TMS + PNS) with task-specific practice. During PCMS rest participants will receive PCMS (TMS + PNS) without task-specific practice. During Task-specific sham-PCMS participants will receive task-specific practice with sham PCMS (TMS + PNS).
Arm Title
Task-specific sham-PCMS, Task-specific PCMS, PCMS-rest
Arm Type
Experimental
Arm Description
During Task-specific PCMS participants will receive PCMS (TMS + PNS) with task-specific practice. During PCMS rest participants will receive PCMS (TMS + PNS) without task-specific practice. During Task-specific sham-PCMS participants will receive task-specific practice with sham PCMS (TMS + PNS).
Arm Title
Task-specific sham-PCMS, PCMS-rest, Task-specific PCMS
Arm Type
Experimental
Arm Description
During Task-specific PCMS participants will receive PCMS (TMS + PNS) with task-specific practice. During PCMS rest participants will receive PCMS (TMS + PNS) without task-specific practice. During Task-specific sham-PCMS participants will receive task-specific practice with sham PCMS (TMS + PNS).
Intervention Type
Device
Intervention Name(s)
Task-specific PCMS
Intervention Description
120 pairs of TMS and PNS volleys will be administered during electromyography-triggered functional electrical stimulation (FES)-assisted task-specific training (task-specific PCMS). In the task-specific PCMS, participants will first grasp a spherical ball when prompted by an auditory 'Ready' cue, and upon seeing a visual 'Go' cue will voluntarily extend the wrist and fingers to release the ball. After the 'Go cue', our customized stimulation delivery algorithm triggers the TMS and PNS only when the extensor digitorum communis (EDC) muscle activity exceeds a pre-determined threshold. The algorithm will then trigger FES to EDC after detecting EDC activity (~2 ms after PNS) for the next 2 seconds, allowing the pairing of PCMS (TMS and PNS) with the voluntary movement of EDC without the confounding effects of FES.
Intervention Type
Device
Intervention Name(s)
Task-specific sham-PCMS
Intervention Description
120 pairs of sham-PCMS stimuli will be administered during task-specific practice. The TMS coil will be placed ~10 cm behind the participant's head, and PNS electrodes will be placed in the same position as for task-specific PCMS, but no stimulation will be delivered. Like the task-specific PCMS condition, participants will perform the same grasp and release a ball task in an identical manner. FES will be delivered after detecting voluntary EDC activity, similar to the task-specific PCMS condition.
Intervention Type
Device
Intervention Name(s)
PCMS-rest
Intervention Description
120 pairs of TMS and PNS volleys will be administered with the EDC muscle at rest every 10 s (~20 min, 0.1 Hz). TMS will be used to elicit motor-evoked potentials (MEPs). Antidromic activation of spinal motor neurons will be elicited by supramaximal peripheral nerve stimulation (PNS) applied to the radial nerve near the elbow. Volleys will be timed to arrive in the spinal cord based on central and peripheral conduction times calculated for each subject so that the pre-synaptic terminal is depolarized via TMS ~1-2 ms before spinal motor neurons are depolarized via PNS at a pulse duration of 200us. We will also perform stimulation of the cervical roots (C-root) by placing the coil behind the neck and stimulating the C-root (C6 and C7 vertebrae), which innervate the finger extensor muscles. Conduction times will be calculated from latencies of the primary motor area (M1) MEP, C-root, and M-wave.
Primary Outcome Measure Information:
Title
Transcranial magnetic stimulation to evaluate corticospinal transmission
Description
Corticospinal transmission will be assessed by examining the percent change of the peak-to-peak motor evoked potential (MEP) amplitude relative to baseline.
Time Frame
Change from baseline up to 30-minutes post intervention
Secondary Outcome Measure Information:
Title
Voluntary force production to evaluate motor performance
Description
We will measure force production of the wrist and finger extensors (EDC) to evaluate motor performance using load cells embedded in cushioned customized platforms. Participants will perform isometric wrist and finger extension movements against load cells. We will calculate the percent change of maximum force output.
Time Frame
Change from baseline up to 30-minutes post intervention
Title
Maximum finger excursions to evaluate motor performance
Description
Three-dimensional biomechanical data will be collected to evaluate motor performance using a motion capture system. Reflective markers will be placed on the participant's paretic forearm, hand, and fingers to track wrist and finger movements during a maximum hand opening task. Hand biomechanics will be evaluated by computing the percent change of maximum finger excursions during the hand opening task.
Time Frame
Change from baseline up to 30-minutes post intervention
Title
Maximum finger spread to evaluate motor performance
Description
Three-dimensional biomechanical data will be collected to evaluate motor performance using a motion capture system. Reflective markers will be placed on the participant's paretic forearm, hand, and fingers to track wrist and finger movements during a maximum hand opening task. Hand biomechanics will be evaluated by computing the percent change of maximum finger spread during the hand opening task.
Time Frame
Change from baseline up to 30-minutes post intervention
Title
Box and Block Test
Description
The Box and Block Test (BBT) measures unilateral gross manual dexterity and the ability to release objects. We will calculate the percent change of the total number of blocks transferred in one minute.
Time Frame
Change from baseline up to 30-minutes post intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 18-80 years Diagnosis of first-ever subcortical stroke (single cerebrovascular accident) Stroke onset of at least six months prior to the time of participation A score of at least 1 out of 2 on the spherical grasping item of the Fugl-Meyer Upper Extremity Subscale to allow participants to grasp the ball Cognitive skills to actively participate, as indicated by scores of > 23 on the Mini-Mental Status Examination English speaking Exclusion Criteria: Inability to elicit a motor evoked potential (MEP) in the EDC muscle even with a 20% background muscle contraction Presence of severe aphasia Excessive spasticity of the wrist and finger muscles, defined as a Modified Ashworth Score >2 Diagnosis of neurological disorders other than stroke History of seizure or epilepsy Orthopedic/musculoskeletal conditions (e.g., arthritis) affecting the upper extremity Presence of metallic implants in the head or neck Currently or planning to become pregnant Difficulty maintaining alertness or remaining still Ferromagnetic metallic implants, pacemakers, other implanted devices, or ventilators for magnetic resonance imaging (MRI) Bodyweight > 300 lbs due to MRI scanner dimensions (for subjects also undergoing MRI) Psychiatric diagnosis according to the criteria of the Diagnostic and Statistical Manual of Mental Disorder, Fifth Edition (DSM-V), or who are on psychotropic medication Life expectancy less than the duration of the study Excessive pain in the paretic hand, defined as a Visual Analog Scale Score >4 Participation in concurrent occupational therapy Current use of recreational drugs and stimulants like cocaine and methylenedioxymethamphetamine (MDMA)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Amit Sethi, PhD
Phone
4123836619
Email
asethi@pitt.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amit Sethi, PhD
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
Neuromotor Recovery and Rehabilitation Lab
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15260
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Amit Sethi
Phone
412-383-6619
Email
asethi@pitt.edu

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

PCMS Task After Moderate-to-severe Stroke

We'll reach out to this number within 24 hrs