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Bracing for Walking in Parkinson's Disease

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Completed

Conditions

Gait Disorders, Neurologic
Parkinson Disease

Treatments

Device: Carbon Fiber Ankle Foot Orthosis (AFO)
Other: Standardized walking/exercise program

Study type

Interventional

Funder types

Other

Identifiers

NCT03192046
STU 012014-059

Details and patient eligibility

About

Parkinson disease (PD) is a progressive neurological disease that results in characteristic gait dysfunction. Gait problems include decreased velocity, decreased stride length, difficulty with initiation of gait, postural stability problems and alteration in joint kinematics.1 In this typically older patient population, these gait deviations affect their participation in household and community activities. The standard of care is currently focused on therapeutic exercise and cueing of various types (visual, auditory, verbal). Current interventions have not been demonstrated to markedly improve gait kinematics, so there is a need to identify interventions that could improve gait performance in this population. Lower extremity bracing is a common and well-established intervention for gait dysfunction with other populations, including stroke and brain injury. The braces allow for improved stability, sensory feedback, and consistent tactile cues to allow patients to have the best gait mechanics with each step. It is reasonable to hypothesize that appropriate bracing may have the potential to improve gait function and kinematics in PD since these patient often have gastroc-soleus weakness. Data from our early pilot studies indicates that bracing individuals with PD can positively impact their mobility. This includes improvements in velocity, step length, and dynamic balance. Additional data supported an upward trend in quality of life.

Full description

This is a randomized, repeated measures, matched group study. There will be two groups of participants, 8 participants per group, 35 participants total from time of initial enrollment in this study. Group one (G1) will receive bilateral custom braces and a standardized home walking/exercise program. Group two will receive the standardized walking/exercise program without any brace or AFO. Subjects will be randomized upon enrollment in the study. At the time of consent, random drawing from concealed envelopes with red, blue or green chips will be done to determine group assignment. Subjects will be recruited through the Clinical Center for Movement Disorders at UT Southwestern Medical Center where patients with PD receive routine evaluation and follow-up. Subjects will be followed for 6 months during this study and outcome measures will be collected 3 times over the course of the study. Subjects will be seen every 3 months for the duration of the study for testing as well as for other visits as noted in the table below. Participants will not need to have insurance benefits for initial physical therapy evaluation and for ankle braces. All subsequent visits to the Crowley gait lab for assessments and brace adjustment will be provided at no cost to the participants.

Enrollment

10 patients

Sex

All

Ages

30 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Confirmed diagnosis of Parkinson's Disease according to the UK brain bank criteria.5
  2. Age between 30 and 85.
  3. Measurable decrement in gait velocity (between 35 and 15 percent below age-predicted norms for self-selected walking velocity) as measured by the 6 MWT
  4. Hoehn and Yahr stage 2-3.
  5. Less than 10 full heel raises in single limb stance bilaterally.

Exclusion criteria

  1. Body mass index greater than 40.
  2. Passive dorsiflexion range of motion less than approximately neutral (90 degrees)
  3. Any other uncontrolled health condition for which gait training is contraindicated
  4. Self-report of > 1 fall/month
  5. A score of 11 or less on the Short Orientation-Memory-Concentration Test of Cognitive Impairment

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

10 participants in 2 patient groups

Carbon Fiber Ankle Foot Orthosis (AFO)
Experimental group
Description:
For the bracing group, the participants will wear custom fabricated carbon fiber braces in addition to participating in a daily walking program and 7 visits of PT.
Treatment:
Device: Carbon Fiber Ankle Foot Orthosis (AFO)
Control Group, Walking Program Only
Active Comparator group
Description:
The participants in this group will be prescribed a daily home walking walking program and 7 visits of PT.
Treatment:
Other: Standardized walking/exercise program

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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