Neural Adaptation After Tendon Transfer and Training in Tetraplegia

Sponsor
VA Office of Research and Development (U.S. Fed)
Overall Status
Completed
CT.gov ID
NCT02768103
Collaborator
(none)
5
1
1
26
0.2

Study Details

Study Description

Brief Summary

The number of people in the United States who have survived SCI is estimated to be approximately 273,000 persons. Around 50% of the injuries are to the cervical spine resulting in tetraplegia. An important rehabilitation goal in this population is recovery of upper limb function, which could decrease medical costs and improve their quality of life. Re-establishing active grasp and pinch strength to the hand can be accomplished by surgeries that transfer the tendon of a strong muscle to restore strength to a paralyzed muscle, but the outcomes of the surgeries are variable. The investigators have demonstrated in an ongoing study, the functional gains after surgery can be improved with a focused therapy program to retrain the transferred muscle. The propose of this study is to examine the cortical mechanisms that drive successful muscle re-education after surgery. Understanding the neural (brain) activity associated with functional performance can help to predict who will respond to therapy and will guide evidence-based rehabilitation programs to improve upper limb function in tetraplegia.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: task-based training
N/A

Detailed Description

Restoring upper limb function is rated among the highest priorities for individuals with tetraplegia. Re-establishing active grasp and pinch strength to the hand can be accomplished by tendon transfer procedures in which the tendon of a strong proximal muscle is surgically re-attached to the tendon of a paralyzed muscle. A common procedure to restore lateral (key) pinch is to transfer the distal tendon of one of the three elbow flexor muscles, the brachioradialis (Br) to the tendon of the paralyzed thumb flexor, the flexor pollicis longus (FPL). Recovery of functional pinch depends on how well the patient learns to activate the Br to flex the thumb through its new distal attachment, and also to control flexion at the elbow through its proximal attachment. The investigators' previous work shows that Br to FPL recipients do not activate the transferred Br fully and may not reach optimal functional status on their own or with traditional therapies. The investigators propose that participation in a postoperative task-based training program will drive cortical changes that impact functional (pinch) ability.

Recent studies of individuals with cervical SCI show substantial cortical reorganization can occur after the injury, but neural substrates of motor learning after tendon transfer have not been studied. For these patients, very little is known about what functional brain changes accompany improved performance in response to additional intervention. The Br to FPL transfer alters the central feedback from the periphery and may permit new or adaptive neural pathways that can achieve greater functional use of the tendon transfer. Neuroimaging techniques, such as functional magnetic resonance imaging (fMRI) have become important tools for understanding plasticity in the neuromuscular system and for assessing the neural underpinnings of successful novel interventions. The objective of the proposed study is to identify the neural pattern that is associated with the best functional outcomes (highest pinch force) after Br to FPL transfer. The investigators will use fMRI and functional performance measures to find neural predictors and correlates of muscle re-education. That is, the investigators expect that successful postoperative muscle re-education will depend on increased cortical drive to the transferred Br in combination with new synergists, and this will be reflected in the neural imaging results.

The purpose of the study is to evaluate neural activity from Br to FPL transfer recipients after conventional therapy and in response to an additional task-based training home program that aims to improve voluntary activation of the transferred Br in functional pinch tasks. The 10-week training program is under evaluation in RRD Pilot (B0583P) study and includes producing pinch force in different upper limb postures, biofeedback from a pinch dynamometer, and practicing selected pinch tasks. The investigators anticipate that increases in the amplitude and distribution of fMRI blood oxygen level dependent (BOLD) responses in sensorimotor cortices will underlie improved motor control post-surgically and following successful intervention to promote motor relearning.

Specific Aims

  1. Define the cortical representation of pre-training pinch function in SCI patients. The investigators will quantify the pattern (location, volume and intensity) of cortical activation associated with voluntary pinch in individuals who are one-year post Br to FPL tendon transfer surgery and a conventional therapy program. The investigators hypothesize (H1) greater volume and intensity of brain activation will correlate to better pinch function measured by pinch strength and the magnitude Br activation in pinch. Secondary analyses will determine if the location of the brain activation varies with pinch function (force) and specificity relative to voluntary elbow flexion.

  2. Evaluate the cortical response to the task-based home therapy program. Correlates of task-based adaptation from pre- to post-training will be assessed using fMRI. H2: Greater activation (intensity and volume) in the primary motor cortex (M1) and sensory cortex will translate to increased voluntary activation of the transferred Br in pinch compared to elbow flexion. Task-based training outcome measures will include isometric pinch force magnitude, EMG quantification of Br activation in pinch and elbow flexion.

  3. Determine neural signatures of surgical and training induced motor improvements. H3: After directed task-based training, brain activity during voluntary pinch will extend to adjacent areas (larger representation, greater activity), in sensorimotor brain areas, facilitating the ability to voluntarily increase the transferred Br activation in pinch. Secondary analyses will contrast size and activation level of brain changes with pinch activation in patients who receive training relative to non-impaired and non-surgical participants.

The postoperative therapy protocols after tendon transfer procedures are not well defined, inconsistently applied, and lack evidence for their effectiveness. The study proposed here will investigate cortical change to assess outcome dependent plasticity. Thus, it may be possible to predict why some individuals do not re-train the transferred muscle as well as others. Establishing this relationship can lead to understanding the mechanisms of successful interventions and may identify brain based dynamics that could become the focus of future treatments (e.g. biofeedback, brain stimulation, etc.).

Study Design

Study Type:
Interventional
Actual Enrollment :
5 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
All participants complete 10 week task based training in home setting.All participants complete 10 week task based training in home setting.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Evaluating Neural Adaptation After Tendon Transfer and Task-based Training in SCI
Actual Study Start Date :
May 1, 2016
Actual Primary Completion Date :
Jun 30, 2018
Actual Study Completion Date :
Jun 30, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: SCI transfer + training

Individuals with tetraplegia and brachioradialis to flexor pollicis longus transfer will participate in 10 week home training program to improve surgical outcome (pinch strength)

Behavioral: task-based training
The 10-week training program is designed to incorporate requirements of motor learning and includes activities that require learning to coordinate the transferred Br with other synergists by producing pinch force in different upper limb postures and in a range of pinch openings. Biofeedback using a pinch dynamometer in self-selected postures provides feedback and knowledge of progress to the participant. A task board is used for practicing task-specific activities such as opening and closing zippers, using a remote, an ATM card, a key, and an electrical plug and focuses on pinch in dynamic conditions that require modulating force and maintaining specific positions. The pinch-pin device requires closing pinch-pins (clothes pin) of variable resistance ranging from approximately 1 to 8 lbs and placing them on rods arranged at different positions in the work space.

Outcome Measures

Primary Outcome Measures

  1. Pinch Force [after 10 weeks home exercise program with task-based training]

    Pinch force recorded in newtons from force sensor mounted to a custom grip

  2. Functional MRI BOLD Signal From Motor Cortex [after 10 week home exercise program with task-based training]

    A block design with 10 seconds of rest alternating with 10 seconds of functional movement for 6 minutes will be followed. Participants have visual cues to instruct them in the timing and sequence of the tasks to be performed. Scan time to include a session of elbow flexion and a session for pinch is about 20 minutes. The main outcome measures for the fMRI data will be brain activation defined by intensity and cluster size in response to performing elbow flexion and pinch. Second level analyses will be mixed models effects derived using FSL FLAME for within subjects (pre to post intervention) as well as cross-sectional (non impaired vs. SCI-ns; SCI-ns vs. SCI+TT) individual models (with outlier deweighting and standard settings).

Secondary Outcome Measures

  1. Fine-wire Electromyography of Transferred Brachioradialis Muscle (to Paralyzed Thumb Flexor) [after 10 week home exercise program with task-based training]

    EMG signal recorded from fine-wire (intramuscular) electrodes normalized to a maximum voluntary contraction

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Individuals with a clinical diagnosis of SCI cervical level 4-7, complete or incomplete injuries, who have completed conventional therapy and be at least 1-year post-surgery, are eligible for the study.

  • Participants must have had Br to FPL tendon transfer, be willing to participate in a 10 week exercise program, have adequate assistance or be independent in setting up exercise equipment (weight cuffs, functional tasks), and be available for two measurement sessions.

  • Women and minorities may be included in the study if they meet the inclusion criteria.

  • Non-Veteran participants who meet the selection criteria will be included to expand the available number of subjects.

Exclusion Criteria:
  • More than one tendon transfer to the thumb to restore pinch but not if they have other tendon transfer procedures on the same upper limb.

  • Other exclusion criteria include pain that would limit their ability to perform the activities, spasticity in the upper limb, or spinal cord injury level above C4 or below C7 as their pattern of weakness will be substantially different.

  • Subjects who are participating in other research studies that include exercise programs for the upper limb or drug studies that affect their response to exercise will also be excluded.

Contacts and Locations

Locations

Site City State Country Postal Code
1 VA Palo Alto Health Care System, Palo Alto, CA Palo Alto California United States 94304-1290

Sponsors and Collaborators

  • VA Office of Research and Development

Investigators

  • Principal Investigator: Mary E Johanson, DPT, VA Palo Alto Health Care System, Palo Alto, CA

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
VA Office of Research and Development
ClinicalTrials.gov Identifier:
NCT02768103
Other Study ID Numbers:
  • N1772-P
First Posted:
May 11, 2016
Last Update Posted:
Apr 15, 2020
Last Verified:
Apr 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by VA Office of Research and Development
Additional relevant MeSH terms:

Study Results

Participant Flow

Recruitment Details
Pre-assignment Detail
Arm/Group Title SCI Transfer + Training
Arm/Group Description Individuals with tetraplegia and brachioradialis to flexor pollicis longus transfer will participate in 10 week home training program to improve surgical outcome (pinch strength) task-based training: 10-week training program incorporates activities that require learning to coordinate the transferred Br with other synergists by producing pinch force in different upper limb postures and in a range of pinch openings. Biofeedback using a pinch dynamometer in self-selected postures provides feedback to the participant. A task board is used for practicing task-specific activities such as opening and closing zippers, using a remote, an ATM card, a key, and an electrical plug and focuses on pinch in dynamic conditions that require modulating force and maintaining specific positions. The pinch-pin device requires closing pinch-pins (clothes pin) of variable resistance ranging from approximately 1 to 8 lbs and placing them on rods arranged at different positions in the work space.
Period Title: Overall Study
STARTED 5
COMPLETED 4
NOT COMPLETED 1

Baseline Characteristics

Arm/Group Title SCI Transfer + Training
Arm/Group Description Individuals with tetraplegia and brachioradialis to flexor pollicis longus transfer will participate in 10 week home training program to improve surgical outcome (pinch strength) task-based training: 10-week training program incorporates activities that require learning to coordinate the transferred Br with other synergists by producing pinch force in different upper limb postures and in a range of pinch openings. Biofeedback using a pinch dynamometer in self-selected postures provides feedback to the participant. A task board is used for practicing task-specific activities such as opening and closing zippers, using a remote, an ATM card, a key, and an electrical plug and focuses on pinch in dynamic conditions that require modulating force and maintaining specific positions. The pinch-pin device requires closing pinch-pins (clothes pin) of variable resistance ranging from approximately 1 to 8 lbs and placing them on rods arranged at different positions in the work space.
Overall Participants 4
Age (Count of Participants)
<=18 years
0
0%
Between 18 and 65 years
4
100%
>=65 years
0
0%
Sex: Female, Male (Count of Participants)
Female
2
50%
Male
2
50%
Ethnicity (NIH/OMB) (Count of Participants)
Hispanic or Latino
0
0%
Not Hispanic or Latino
4
100%
Unknown or Not Reported
0
0%
Pinch force (Newtons) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [Newtons]
8.7
(6.5)

Outcome Measures

1. Primary Outcome
Title Pinch Force
Description Pinch force recorded in newtons from force sensor mounted to a custom grip
Time Frame after 10 weeks home exercise program with task-based training

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title SCI Transfer + Training
Arm/Group Description Individuals with tetraplegia and brachioradialis to flexor pollicis longus transfer will participate in 10 week home training program to improve surgical outcome (pinch strength) task-based training: 10-week training program incorporates activities that require learning to coordinate the transferred Br with other synergists by producing pinch force in different upper limb postures and in a range of pinch openings. Biofeedback using a pinch dynamometer in self-selected postures provides feedback to the participant. A task board is used for practicing task-specific activities such as opening and closing zippers, using a remote, an ATM card, a key, and an electrical plug and focuses on pinch in dynamic conditions that require modulating force and maintaining specific positions. The pinch-pin device requires closing pinch-pins (clothes pin) of variable resistance ranging from approximately 1 to 8 lbs and placing them on rods arranged at different positions in the work space.
Measure Participants 4
Pre-training pinch force (N)
8.7
(6.5)
Post-training pinch force (N)
10.6
(8.6)
2. Primary Outcome
Title Functional MRI BOLD Signal From Motor Cortex
Description A block design with 10 seconds of rest alternating with 10 seconds of functional movement for 6 minutes will be followed. Participants have visual cues to instruct them in the timing and sequence of the tasks to be performed. Scan time to include a session of elbow flexion and a session for pinch is about 20 minutes. The main outcome measures for the fMRI data will be brain activation defined by intensity and cluster size in response to performing elbow flexion and pinch. Second level analyses will be mixed models effects derived using FSL FLAME for within subjects (pre to post intervention) as well as cross-sectional (non impaired vs. SCI-ns; SCI-ns vs. SCI+TT) individual models (with outlier deweighting and standard settings).
Time Frame after 10 week home exercise program with task-based training

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title
Arm/Group Description
3. Secondary Outcome
Title Fine-wire Electromyography of Transferred Brachioradialis Muscle (to Paralyzed Thumb Flexor)
Description EMG signal recorded from fine-wire (intramuscular) electrodes normalized to a maximum voluntary contraction
Time Frame after 10 week home exercise program with task-based training

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title SCI Transfer + Training
Arm/Group Description Individuals with tetraplegia and brachioradialis to flexor pollicis longus transfer will participate in 10 week home training program to improve surgical outcome (pinch strength) task-based training: 10-week training program incorporates activities that require learning to coordinate the transferred Br with other synergists by producing pinch force in different upper limb postures and in a range of pinch openings. Biofeedback using a pinch dynamometer in self-selected postures provides feedback to the participant. A task board is used for practicing task-specific activities such as opening and closing zippers, using a remote, an ATM card, a key, and an electrical plug and focuses on pinch in dynamic conditions that require modulating force and maintaining specific positions. The pinch-pin device requires closing pinch-pins (clothes pin) of variable resistance ranging from approximately 1 to 8 lbs and placing them on rods arranged at different positions in the work space.
Measure Participants 4
pre-training normalized Br EMG
30
(10)
post training normalized Br EMG
34
(10)

Adverse Events

Time Frame Adverse event data were collected during the 10 week training period.
Adverse Event Reporting Description
Arm/Group Title SCI Transfer + Training
Arm/Group Description Individuals with tetraplegia and brachioradialis to flexor pollicis longus transfer participate in 10 week home training program to improve surgical outcome (pinch strength). The 10-week training program includes activities that require learning to coordinate the transferred Br with other synergists by producing pinch force in different upper limb postures and in a range of pinch openings. Biofeedback using a pinch dynamometer in self-selected postures provides feedback and knowledge of progress to the participant. A task board is used for practicing task-specific activities such as opening and closing zippers, using a remote, an ATM card, a key, and an electrical plug and focuses on pinch in dynamic conditions that require modulating force and maintaining specific positions. The pinch-pin device requires closing pinch-pins (clothes pin) of variable resistance ranging from approximately 1 to 8 lbs and placing them on rods arranged at different positions in the work space.
All Cause Mortality
SCI Transfer + Training
Affected / at Risk (%) # Events
Total 0/4 (0%)
Serious Adverse Events
SCI Transfer + Training
Affected / at Risk (%) # Events
Total 0/4 (0%)
Other (Not Including Serious) Adverse Events
SCI Transfer + Training
Affected / at Risk (%) # Events
Total 0/4 (0%)

Limitations/Caveats

[Not Specified]

More Information

Certain Agreements

All Principal Investigators ARE employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

Results Point of Contact

Name/Title Dr Johanson
Organization VA Palo Alto Health Care System
Phone 408-250-1982
Email lisa.johanson29@gmail.com
Responsible Party:
VA Office of Research and Development
ClinicalTrials.gov Identifier:
NCT02768103
Other Study ID Numbers:
  • N1772-P
First Posted:
May 11, 2016
Last Update Posted:
Apr 15, 2020
Last Verified:
Apr 1, 2020