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Clinical Use of Andante SmartStep System in Gait Rehabilitation

Clinical Use of Andante SmartStep System in Gait Rehabilitation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00268658
Enrollment
60
Registered
2005-12-22
Start date
Unknown
Completion date
Unknown
Last updated
2007-02-27

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

Conditions

Ankle Injuries, Femoral Neck Fractures

Keywords

Arthroplasty, Replacement, Hip, Arthroplasty, Replacement, Knee, Arthroscopy

Brief summary

The purpose of this study is to evaluate the effectiveness of the biofeedback gait training device in improving load bearing over an operated limb, during post-operative gait training therapy. The effectiveness of the device will also be tested in self-training at home.

Detailed description

To evaluate the effectiveness of the biofeedback gait training device as a biofeedback training therapeutic tool in improving body-weight bearing over the affected lower limb, quality of gait, level of ambulation and physical independence during rehabilitation, in patients after orthopedic procedures during gait therapy training, and as a biofeedback device for self-training at home.

Interventions

DEVICESmartStep(tm) biofeedback device

Sponsors

Soroka University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Rehabilitation after operation * Patient is allowed full weight bearing * Patient is motivated and able to communicate and understands orders * Patient is able to walk 10 meters * Patient filled out agreement and consent form

Exclusion criteria

* Activity limitation due to medical disorder, medications, or emotional status. * Pain markedly obstructs gait ability * Documented peripheral neuropathy * Functional limitation prior to the current condition * Premorbid, ongoing major depression or psychosis * Multiple/pathological fractures * Serious early complications * Terminally ill patients * Pregnant women * Participation in current or recent (within 60 days prior to surgery) clinical trial

Design outcomes

Primary

MeasureTime frame
load bearing over the affected lower limb
quality/symmetry of gait
level of ambulation and physical independence

Countries

Israel

Outcome results

None listed

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