Muscle Fatigue and Scapular Sensorimotor System
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| ClinicalTrials.gov Identifier: NCT03066102 |
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Recruitment Status :
Completed
First Posted : February 28, 2017
Results First Posted : July 15, 2019
Last Update Posted : July 29, 2019
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Muscle; Fatigue | Other: muscle fatigue | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 30 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Other |
| Official Title: | Muscle Fatigue and Scapular Sensorimotor System |
| Actual Study Start Date : | July 1, 2017 |
| Actual Primary Completion Date : | August 11, 2017 |
| Actual Study Completion Date : | March 27, 2018 |
- Other: muscle fatigue
Modified push-up plus exercise:
the participants first supported by both knees and the single elbow, and then performed sustained scapular protraction for three minutes with ten repetitions in males and two minutes with five repetitions in females with forty-five seconds rest between.
- Change From Baseline in Scapular Proprioception [ Time Frame: through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects ]Test the ability of active re-position the scapula from neutral to 90% range of protraction, and elevation.
- Change From Baseline in Muscle Activation During Scapular Proprioception [ Time Frame: through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects ]
Test the ability of muscle activation (upper trapezius, lower trapezius, and serratus anterior) during active re-position the scapula from neutral to 90% range of protraction, and elevation.
Muscle activation during active re-position would divide into muscle activation during maximum voluntary isometric contraction (MVIC), present in percent.
- Change From Baseline in Scapular Muscle Strength [ Time Frame: through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects ]use dynamometer to detect the force of maximum isometric voluntary contraction of upper trapezius, lower trapezius and serratus anterior
- Change From Baseline in Shoulder Kinematics Data During Shoulder Elevation in the Scapular Plane [ Time Frame: through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects ]use Liberty to detect the motion of spine, humerus, and scapula during shoulder elevation in the scapular plane (scaption)
- Change From Baseline in Scapular Muscle Activity During Shoulder Elevation in the Scapular Plane [ Time Frame: through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects ]
Test the ability of muscle activity (upper trapezius, lower trapezius, and serratus anterior) during shoulder elevation in the scapular plane (scaption).
Muscle activation during scaption would divide into muscle activation during maximum voluntary isometric contraction (MVIC), present in percent.
- Change From Baseline in Scapular Muscle Recruitment Timing During Arm Elevation in Scapular Plane [ Time Frame: through fatigue intervention completion, an average of 20 minutes in female subjects and 40 minutes in male subjects ]
Test the ability of muscle onset timing (upper trapezius, lower trapezius, and serratus anterior) during shoulder elevation in the scapular plane (scaption).
Onset timing was determined by EMG signals bigger than resting signals plus 3 times standard deviations.
Origin was set at onset of kinematics data of glenohumeral joint.
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| Ages Eligible for Study: | 20 Years to 40 Years (Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- no shoulder, cervical, and thoracic spine pain within six months
- negative for subacromial impingement test
- normal range of motion of glenohumeral joint
Exclusion Criteria:
- history of dislocation, fracture, or surgery of shoulder joint
- history of central nervous system disorder, rheumatoid arthritis, shoulder osteoarthritis, or cervical radiculopathy
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03066102
| Taiwan | |
| National Yang Ming University | |
| Taipei, Taiwan, 11221 | |
Documents provided by Yi-Fen Shih, National Yang Ming University:
| Responsible Party: | Yi-Fen Shih, Associate Professor, National Yang Ming University |
| ClinicalTrials.gov Identifier: | NCT03066102 |
| Other Study ID Numbers: |
YM105067E |
| First Posted: | February 28, 2017 Key Record Dates |
| Results First Posted: | July 15, 2019 |
| Last Update Posted: | July 29, 2019 |
| Last Verified: | July 2019 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Undecided |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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sensorimotor system scapular joint position sense fatigue |
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Fatigue |

