- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04218175
Effects of Neuromobilization on Median Nerve Elasticity
Purpose: The aim of this study was to investigate the effect of median nerve neuromobilization on median nerve elasticity using shear wave elastography.
Methods: The study included 36 healthy volunteers (72 upper extremities) aged 18-30 years. Inclusion criteria; no known systemic neuromuscular and metabolic diseases, no nerve impingement syndrome, and no upper extremity bone-tendon-muscle surgery in the last six months. Sociodemographic data of the participants were recorded. Wrist flexion and extension bilaterally with universal goniometer and finger grip strength bilaterally were measured with pinchmeter. Median Nerve Stress Test was performed. Median nerve elasticity was measured by Shear Wave Ultrasound Elastography. The extremity of the dominant side as a study group and the non-dominant side as a control group were measured bilaterally. Median nerve neuromobilization (stretching (n = 18) and shifting (n = 18)) was applied to the upper extremities of the dominant side. The application was carried out as 3 sets in one session. Evaluations were repeated after application.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Istanbul, Turkey, 34010
- Istinye University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 18-30 years of age
- Healthy individuals without any known systemic disease
Exclusion Criteria:
- Those who have undergone an upper extremity bone-tendon-muscle operation in the last six months
- People with a systemic disease such as rheumatoid arthritis, diabetes mellitus
- Patients with any neuromuscular disease
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: neuromobilization stretching group
In the neuromobilization stretching group; The subjects were brought to shoulder depression and 90 degrees of abduction while the dominant side forearms were supination.
In this position, median nerve stretching was performed by extending the participant's head to the opposite side while flexing the wrist and finger.
After waiting for 30 seconds in this position, the wrist and head were moved to the neutral position and the participants relaxed.
|
Median nerve neuromobilization (stretching and shifting) was performed.
For median nerve stretching; The subjects were brought to shoulder depression and 90 degrees of abduction while the dominant side forearms were supination.
In this position, median nerve stretching was performed by extending the participant's head to the opposite side while flexing the wrist and finger.
After waiting for 30 seconds in this position, the wrist and head were moved to the neutral position and the participants relaxed.
For median nerve shift; The subjects were brought to shoulder depression and 90 degrees of abduction while the dominant side forearms were supination.
In this position, the participant flexed his wrist and fingers while lateral flexion of his head to the opposite side, and flexed his wrist and fingers while lateral flexion of the head to the same side.
|
EXPERIMENTAL: neuromobilization shifting group
In the neuromobilization shifting group, the subjects were brought to shoulder depression and 90 degrees of abduction while the dominant forearms were supination.
In this position, the participant flexed his wrist and fingers while lateral flexion of his head to the opposite side, and flexed his wrist and fingers while lateral flexion of the head to the same side.
Thus, the participants performed median nerve shift.
|
Median nerve neuromobilization (stretching and shifting) was performed.
For median nerve stretching; The subjects were brought to shoulder depression and 90 degrees of abduction while the dominant side forearms were supination.
In this position, median nerve stretching was performed by extending the participant's head to the opposite side while flexing the wrist and finger.
After waiting for 30 seconds in this position, the wrist and head were moved to the neutral position and the participants relaxed.
For median nerve shift; The subjects were brought to shoulder depression and 90 degrees of abduction while the dominant side forearms were supination.
In this position, the participant flexed his wrist and fingers while lateral flexion of his head to the opposite side, and flexed his wrist and fingers while lateral flexion of the head to the same side.
|
NO_INTERVENTION: Control Group
The dominant sides of the individuals are experimental sides and the other nondominant sides of the participants are control sides.
And no intervention was made.
All measurements were done bilaterally before and after.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Median Nerve Tension Test
Time Frame: 4 weeks
|
The test was performed in a position with shoulder depression and 90 degrees abduction and external rotation, elbow 90 degrees flexion, forearm full supination, and wrist and fingers fully extended.
Maintaining this position, the elbow was passively extended and the tension of the median nerve was tested.
The test was stopped at the point where the patient felt pain and tension, and the angle at the elbow was measured by a universal goniometer.
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4 weeks
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Median nerve elasticity with Shear Wave Ultrasound Elastography
Time Frame: 4 weeks
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The nerve elasticity was measured by measuring the velocity of shear waves in the median nerve by means of high frequency ultrasound waves.
|
4 weeks
|
Bilaterally finger grip strength with pinchmeter
Time Frame: 4 weeks
|
finger grip strength was measured bilaterally by pinch meter.
|
4 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 005
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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