- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01266382
The Effect of AposTherapy on the Level of Pain, Function and Quality of Life in Patients With Neuro-muscular and Neurological Disorders
December 23, 2010 updated by: Assaf-Harofeh Medical Center
The purpose of the study is to examine the effect of a new biomechanical device and treatment methodology (AposTherapy) on gait patterns, pain, function and quality of life of patients with musculoskeletal and neurological disorders.
Based on previous reports the investigators hypothesis that this therapy will have a positive effect on these measurements.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Herzliya, Israel, 46733
- Recruiting
- AposTherapy center
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Contact:
- Ganit Segal
- Email: ganitm@apos.co.il
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 85 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Primary osteoarthritis
- Lower limb joint replacement
- Lower limbs fractures
- Spinal disorders including LBP w/wo refered symptoms, radiculopathy, spinal stenosis
- ligaments tear
- Meniscal tears
Exclusion Criteria:
- lack of balance (3 falls in the last year)
- incapable to complete a questionnaire •>age 85
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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WOMAC
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SF-36
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Spatio-temporal Gait parameters
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Secondary Outcome Measures
Outcome Measure |
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FAOS questionnaire
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Oswestry questionnaire
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Clinical measurements
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
December 22, 2010
First Submitted That Met QC Criteria
December 23, 2010
First Posted (Estimate)
December 24, 2010
Study Record Updates
Last Update Posted (Estimate)
December 24, 2010
Last Update Submitted That Met QC Criteria
December 23, 2010
Last Verified
July 1, 2009
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 93/09
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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