Effectiveness of the Astym Technique, the Graston Technique, and Therapeutic Ultrasound in the Treatment of Lateral Epicondylosis.
NCT ID: NCT03234192
Last Updated: 2020-01-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
21 participants
INTERVENTIONAL
2017-06-10
2019-05-23
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
TREATMENT
SINGLE
Study Groups
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Therapeutic ultra sound
Therapeutic ultra sound
This group will receive standard treatment consisting of eccentric strengthening, stretch, proximal strengthening, and education in addition to therapeutic ultra sound treatment.
Astym Treatment Technique
Astym Treatment Technique
This group will receive standard treatment consisting of eccentric strengthening, stretch, proximal strengthening, and education in addition to Astym Treatment.
Graston Treatment Technique
Graston Treatment Technique
This group will receive standard treatment consisting of eccentric strengthening, stretch, proximal strengthening, and education in addition to Graston Treatment.
Interventions
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Therapeutic ultra sound
This group will receive standard treatment consisting of eccentric strengthening, stretch, proximal strengthening, and education in addition to therapeutic ultra sound treatment.
Astym Treatment Technique
This group will receive standard treatment consisting of eccentric strengthening, stretch, proximal strengthening, and education in addition to Astym Treatment.
Graston Treatment Technique
This group will receive standard treatment consisting of eccentric strengthening, stretch, proximal strengthening, and education in addition to Graston Treatment.
Eligibility Criteria
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Inclusion Criteria
* Be able to follow a home exercise program
* Be able to consent to participation in the research study
Exclusion Criteria
* Clients with additional acute orthopedic injuries and/or surgeries to the involved upper extremity will not be included in this study.
* Clients with open wounds of the involved upper extremity that will interfere with treatment techniques will not be involved in this study.
18 Years
ALL
No
Sponsors
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NYU Langone Health
OTHER
Responsible Party
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Principal Investigators
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Steve Vanlew, MD
Role: PRINCIPAL_INVESTIGATOR
NYU Langone Health
Locations
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New York University School of Medicine
New York, New York, United States
Countries
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Other Identifiers
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16-02176
Identifier Type: -
Identifier Source: org_study_id
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