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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT01127685 |
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Date of registration:
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27/04/2010 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Weight-bearing Measuring Device Following Anterior Cruciate Ligament Reconstruction
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Scientific title:
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The Use of a Biofeedback Insole Weight-bearing Measuring Device in Determining Weight-bearing Deficits Following Anterior Cruciate Ligament Reconstruction |
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Date of first enrolment:
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May 2010 |
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Target sample size:
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30 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT01127685 |
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Study type:
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Interventional |
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Study design:
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Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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Phase:
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Phase 1
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Countries of recruitment
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Israel
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Male or female patients more than 18 years old, derivate to physiotherapy treatment
in Lerner Central Sport, Hebrew University - Jerusalem
- Patients who are willing to participate in the trial and to sign the informed consent
forms.
Exclusion Criteria:
- Patients receiving other methods of treatment to this area,
- Patients with concomitant other injury of the hip, knee, ankle or foot.
- Non cooperative patient.
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Weight-bearing Deficits
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Intervention(s)
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Device: Smart_Step weight bearing insole
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Primary Outcome(s)
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The Use of a Biofeedback Insole Weight-bearing Measuring Device in Determining Weight-bearing Deficits Following Anterior Cruciate Ligament Reconstruction
[Time Frame: During their regular training the participants will use the flexible, light weight, force-sensing insole for few minutes to receive the parameters]
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Secondary ID(s)
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MMC10043-2010CTIL
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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