Skip to content

Effect of Orthoses and Underfoot Vibration on Balance in Neuropathy

The Feasibility and Effect of Ankle Foot Orthoses and Underfoot Vibration on the Postural Stability of People With Inherited Neuropathy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03278093
Enrollment
15
Registered
2017-09-11
Start date
2017-10-20
Completion date
2019-02-20
Last updated
2019-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

CMT1A, CMT - Charcot-Marie-Tooth Disease, Hereditary Peripheral Neuropathy, Peripheral Neuropathy

Keywords

Physiotherapy, Physical therapy, Balance, Posturography

Brief summary

A cross-sectional study which will look at the effects of AFO's and vibrating insoles on balance performance in people with CMT disease.

Detailed description

Balance impairments and falls are more common in people who have Charcot Marie Tooth disease (CMT) than in people without the condition. CMT is a condition which affects the nerves causing a variety of symptoms including sensation impairments and weakness. The impairments are usually most evident in the feet and hands, but they can progress very slowly moving closer to the trunk. Ankle Foot Orthoses (AFO's) are often prescribed to help with walking and daily function. So far the effects of AFO's on standing balance in people who have CMT have not been looked at. Insoles are also often prescribed to realign foot deformity and reduce pain. Insoles which give a vibratory input have had a positive impact on walking in older people but have not been looked at in balance and in CMT. Insoles which give a vibration feedback to the sole of the foot when worn have been designed. This study will look at whether the use of AFO's and the vibratory insoles have an effect on standing balance in people with CMT or related peripheral neuropathy. Balance measurements will be taken in a single session comparing a variety of postures. Patients will be recruited from neurology outpatient clinics at the National Hospital of Neurology and Neurosurgery.

Interventions

None listed

Sponsors

University College London Hospitals
CollaboratorOTHER
St George's, University of London
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Clinical or genetically confirmed diagnosis of CMT or related peripheral neuropathy 2. Mixed sensory and motor presentation 3. Over 18 years 4. Able to stand unsupported for five minutes 5. Able to walk for 50m with or without a walking stick or orthotic devices

Exclusion criteria

1. Presence of other significant neurological disorders (such as multiple sclerosis, cerebrovascular diseases, epilepsy, movement disorders), or major comorbidities (e.g. vestibular dysfunction, use of medication which may affect balance, cognitive impairment, presence of medical conditions in which exercise training may be detrimental). 2. Presence of peripheral neuropathy caused by a condition other than CMT. 3. Limb surgery during the six months prior to screening (or planned before final assessment). 4. Women of child-bearing age if they are pregnant, planning a pregnancy during their time in the study or in the 12 weeks following giving birth. This is due to the effects of pregnancy on balance.

Design outcomes

Primary

MeasureTime frameDescription
Posturography30 second caputer in a variety of conditionsCODA motion movement analysis for postural sway Measures will be taken in all conditions with feet together and feet apart. Both conditions will also be looked at with eyes open and eyes closed.
force measures30 second caputer in a variety of conditionsAMTI forceplate for centre of pressure . Measures will be taken in all conditions with feet together and feet apart. Both conditions will also be looked at with eyes open and eyes closed.

Countries

United Kingdom

Contacts

Primary ContactMagdalena Dudziec
m.dudziec@ucl.ac.uk020 3108 7520
Backup ContactGita Ramdharry
g.ramdharry@ucl.ac.uk020 3108 7517

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026