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Control of Unsupported Paraplegic Standing

Integrated Voluntary Control of Unsupported Paraplegic Standing

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00204113
Enrollment
10
Registered
2005-09-20
Start date
2002-06-30
Completion date
Unknown
Last updated
2008-06-13

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

Conditions

Spinal Cord Injury, Stroke

Keywords

spinal cord injury, standing, balance, functional electrical stimulation

Brief summary

The study will investigate the feasibility of using functional electrical stimulation (FES) of the calf muscles of paraplegic subjects to assist in posture stabilisation during standing. We aim to achieve postural stability by combining controlled FES of the lower-limb muscles with the voluntary motor control skills of the intact upper body.

Detailed description

Aim: The study will investigate the feasibility of using functional electrical stimulation (FES) of the calf muscles of paraplegic subjects to assist in posture stabilisation during standing. We aim to achieve postural stability by combining controlled FES of the lower-limb muscles with the voluntary motor control skills of the intact upper body. Background: In spinal cord injury (SCI), the paralysed muscles generally retain their ability to contract and electrical stimulation can be used in rehabilitation as a therapy. With functional electrical stimulation (FES) the aim is to restore some normal motor functions such as standing, stepping or cycling. A number of studies have investigated the physiological effects and potential therapeutic benefits of lower-limb FES exercise. These studies have shown that the benefits include restoration of muscle bulk and strength, a reduction in the rate of bone demineralisation, improvements in the range of joint motion, and relaxation of spasm. Standing is an important part of rehabilitation therapy for paraplegic patients, and helps to alleviate some of the secondary effects of paralysis.

Interventions

DEVICEMulti-purpose rehabilitation frame

Sponsors

University of Glasgow
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum

Inclusion criteria

* Neurologically intact, healthy individuals individuals with complete spinal cord lesion between T6 and T12

Exclusion criteria

* Incomplete SCI

Design outcomes

Primary

MeasureTime frame
estimates of physical parameters (ie. stiffness, viscosity, inertia)

Secondary

MeasureTime frame
quality of standing
amount of sway
timing of standing

Countries

United Kingdom

Outcome results

None listed

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