Musculoskeletal Pain Clinical Trial
Official title:
The Effects of Myofascial Decompression and Neurodynamic Sliding on the Hamstring for Division I Track and Field Athletes With Hamstring Tightness
NCT number | NCT03651141 |
Other study ID # | ED174 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | March 27, 2017 |
Est. completion date | June 12, 2017 |
Verified date | August 2018 |
Source | Oklahoma State University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to investigate the effects of myofascial decompression (cupping) and neurodynamic sliding technique for the hamstring on Division I Track and Field athletes who complain of hamstring tightness. Research questions will be: how do these techniques affect hamstring range of motion and flexibility; isometric strength of the hamstring muscle; muscle activation; and rate of force development. The hypotheses of this study are that neurodynamic sliding will have an effect on all variables and myofascial decompression will only have an effect on range of motion.
Status | Completed |
Enrollment | 21 |
Est. completion date | June 12, 2017 |
Est. primary completion date | April 10, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 25 Years |
Eligibility |
Inclusion Criteria: - Must be in the Sprints, Jumps, or Multi (heptathlon, pentathlon, or decathlon) groups - complain of hamstring tightness and/or injury in the last calendar year - have less than 80° for Active Knee Extension test. Exclusion Criteria: - Past history or current neurological disorders or orthopedic diseases - Surgery of the lower extremity that involves an autograft on the tested leg - Past history of hamstring surgery - Receiving current treatment for a hamstring injury - Received any form of myofascial therapy or neurodynamic techniques within the last week unhealed wounds - active TB - leukemia - hemophilia - thrombocytopenia - fever - influenza - moderate/severe anemia - high blood pressure - cardiac conditions - late stages of pregnancy |
Country | Name | City | State |
---|---|---|---|
United States | Applied Neuromuscular Physiology Lab | Stillwater | Oklahoma |
Lead Sponsor | Collaborator |
---|---|
Oklahoma State University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Hamstring Flexibility change | Using the 'Active Knee Extension test', subjects are placed supine with both the hip and knee positioned at 90° of flexion and then asked to extend lower leg until point of limitation. A digital inclinometer is used to measure the angle of the knee joint in this position to examine flexibility of the hamstring muscle group. | Baseline, 5 minutes after intervention, and within 24 hours of intervention | |
Secondary | Hamstring muscle strength change | Peak torque production of the hamstring muscles will be assessed using an isokinetic dynamometer with the subjects performing a maximum voluntary isometric contraction with the knee in a slightly flexed position. | Baseline, 5 minutes after intervention, and within 24 hours of intervention | |
Secondary | Time of Force Development | Time to reach peak force torque | Baseline, 5 minutes after intervention, and within 24 hours of intervention | |
Secondary | Electromyographic (EMG) Muscle Activation of the Hamstring muscles | The electrical activation signaling of the hamstring muscles will be measured using electromyography during the isometric contraction. | Baseline, 5 minutes after intervention, and within 24 hours of intervention | |
Secondary | Disablement of the Physically Active patient outcome survey | The Disablement of the Physically Active Scale (DPAS) paper survey will be used to assess subject perceptions of impairment, limitation, disability and quality of life related to their hamstring discomfort. The scale ranges from 0 (No disability) to 64 (Severe disability) in which the scores will be compared. | Baseline, 5 minutes after intervention, and within 24 hours of intervention | |
Secondary | Functional Patient Outcome survey | The Lower Extremity Functional Scale is a questionnaire containing 20 questions about a subject's ability to perform everyday tasks. Scores range from 0-4 and represent 'extreme difficulty' or 'unable to perform activity' to 'no difficulty'. The maximum score on the survey is 80 points, with lower total scores indicating a greater perceived disability. | Baseline, 5 minutes after intervention, and within 24 hours of intervention |
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