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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date August 2018
Source Oklahoma State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

Predisposing factors to hamstring injury include neural tension and muscle flexibility restrictions due to fascial adhesions. The sciatic nerve can produce symptoms of pain, decreased range of motion, and increased resting muscle tone when it is overstretched. The nerve can be overstretched after a hamstring injury and cause adhesions on the nerve and abnormal mechanosensitivity leading to perceived hamstring tightness.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.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Neurodynamic Sliding
Subjects in the neurodynamic sliding group perform 2 movements; 1) movement 1 involves sitting on the edge of the treatment table the bringing their neck to their chest along with bending their knee and pointing their ankle to the ground. Movement 2 is performed by facing their head towards the ceiling and straightening their knee while pointing their ankle towards their nose. Subjects will alternate these 2 active movements for 60s and repeated 5 times, with rest period of 15s between sets. A metronome will be set at 30 beats per minute for 15 full slides per minute to standardize the amount of slides per session.
Myofascial Decompression
For the group receiving the cupping treatment, the subject will lay on their stomach and their affected hamstring will be exposed. Cocoa butter will be applied to the hamstring prior to the application of the cups. 5 cups will be placed along the hamstring and calf muscles. Using a handheld suction pump, each cup will be pumped so that skin fills up half of the cup. The cups will stay in place for five minutes and the clinician will instruct the subject to perform 5 repetitions of active quad sets and 5 repetitions of ankle pumps .
Diathermy
The control group will receive a sham heat (diathermy treatment). The subjects will be asked to sit and relax for five minutes and the machine will not be turned on with a timer timing the treatment.

Locations

Country Name City State
United States Applied Neuromuscular Physiology Lab Stillwater Oklahoma

Sponsors (1)

Lead Sponsor Collaborator
Oklahoma State University

Country where clinical trial is conducted

United States, 

Outcome

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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