We updated the design of this site on December 18, 2017. Learn more.
ClinicalTrials.gov Menu

The Effect of Custom-Made Biomechanical Perturbation Platform on Kinetics, Kinematics and Electromyography in Healthy Subjects

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.
ClinicalTrials.gov Identifier: NCT00476333
Recruitment Status : Unknown
Verified April 2007 by Assaf-Harofeh Medical Center.
Recruitment status was:  Recruiting
First Posted : May 22, 2007
Last Update Posted : May 22, 2007
Information provided by:
Assaf-Harofeh Medical Center

Brief Summary:

Introduction: Kinetic, kinematic and electromyographic activity of the lower limb have been shown to be influenced by various footwear-generated biomechanical manipulations (e.g. soles. Insoles, orthoses). A novel biomechanical device comprising four modular elements attached onto foot-worn platforms was recently developed. Each element can be individually calibrated (Position, convexity, height and resilience) to induce a specific biomechanical challenge.

Objectives: The aim of this study is to evaluate the influence of specific biomechanical challenges on Kinetics, kinematics and electromyographic activity of the lower limb.

Design: Prospective, case control Setting: Motion analyses will be conducted during level walking with (1) a three-dimensional motion analysis system and (2) ground reaction force analysis using force platforms (3) Electro-Myography system. Each subject will be examined in 16 different settings of the biomechanical system

Condition or disease Intervention/treatment
Healthy Device: APOS biomechanical gait system

Study Type : Interventional  (Clinical Trial)
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Basic Science

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   20 Years to 30 Years   (Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Healthy
  • Similar anthorpometric profile (i.e. weight, shoe size, height, dominant leg)

Exclusion Criteria:

  • Previous orthopedic, musculosceletal or neurological pathology

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): NCT00476333

Contact: Amir A Haim, MD +972-52-4373010 amirhaim@tx.technion.ac.il
Contact: Alon Wolf, PhD +972-52-6370434 Alonw@tx.technion.ac.il

Technion Israel institute of technology, Biomechanical and bio-robotics division gait laboratory Recruiting
Haifa, Israel
Sub-Investigator: Amir A Haim, MD         
Sub-Investigator: Alon Wolf, PhD         
Principal Investigator: Nahum Halperin, MD         
Sponsors and Collaborators
Assaf-Harofeh Medical Center
Principal Investigator: Nahum Halperin, MD Asaf-Harofeh Medical Center

ClinicalTrials.gov Identifier: NCT00476333     History of Changes
Other Study ID Numbers: 70/07
First Posted: May 22, 2007    Key Record Dates
Last Update Posted: May 22, 2007
Last Verified: April 2007

Keywords provided by Assaf-Harofeh Medical Center: