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The Effect of AposTherapy on the Level of Pain, Function and Quality of Life in Patients With Neuro-muscular and Neurological Disorders

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified July 2009 by Assaf-Harofeh Medical Center.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01266382
First Posted: December 24, 2010
Last Update Posted: December 24, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
Apos Medical and Sports Technology Ltd.
Information provided by:
Assaf-Harofeh Medical Center
  Purpose
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.

Condition Intervention
Osteoarthritis Spinal Diseases Ligament Rupture Lower Extremity Fracture Neurological Disorders Device: AposTherapy

Study Type: Interventional
Study Design: Primary Purpose: Treatment

Resource links provided by NLM:


Further study details as provided by Assaf-Harofeh Medical Center:

Primary Outcome Measures:
  • Spatio-temporal Gait parameters
  • WOMAC
  • SF-36

Secondary Outcome Measures:
  • FAOS questionnaire
  • Oswestry questionnaire
  • Clinical measurements

Intervention Details:
    Device: AposTherapy
    a biomechanical device including 2 hemispheric biomechanical elements attached to a platform in a form of a shoe. the biomechanical device is calibrated to each patient by a physiotherapist specialized with the treatment methodology. patient are instructed to walk indoor with the device. time of exercise is gradually increase
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 85 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

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
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01266382


Contacts
Contact: Ganit Segal, MA ganitm@apos.co.il

Locations
Israel
AposTherapy center Recruiting
Herzliya, Israel, 46733
Contact: Ganit Segal       ganitm@apos.co.il   
Sponsors and Collaborators
Assaf-Harofeh Medical Center
Apos Medical and Sports Technology Ltd.
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
ClinicalTrials.gov Identifier: NCT01266382     History of Changes
Other Study ID Numbers: 93/09
First Submitted: December 22, 2010
First Posted: December 24, 2010
Last Update Posted: December 24, 2010
Last Verified: July 2009

Additional relevant MeSH terms:
Osteoarthritis
Rupture
Nervous System Diseases
Spinal Diseases
Arthritis
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases
Wounds and Injuries
Bone Diseases


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