- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05950360
Kinematics and Muscle Activation of Thoracic Spine and Shoulder in Rock Climbers With Shoulder Pain
November 20, 2023 updated by: Yin-Liang Lin, National Yang Ming University
Background and Purpose: Rock climbing has been a popular sport in recent years.
Rock climbing includes various open-chain and closed-chain arm movements.
Overhead reaching and pull-up are the basic rock climbing elements heavily involving upper extremities.
Different inclination of the wall and terrain also demand sufficient range of motion and strength of the trunk.
Generally overhead reaching and arm elevation may have similar shoulder kinematics, including scapular upward rotation, posterior tilt and external rotation.
Arm elevation usually is accompanied with thoracic extension and unilateral lateral flexion and rotation.
During pull-up, the scapula rotates downward and externally and tilts anterior.
The prevalence of shoulder injuries are about 17%, the second most common among rock climbing injuries.
In the shoulder injuries, shoulder labrum lesions and shoulder impingement are the most common.
Previous studies have shown that individuals with shoulder impingement syndrome have shown decreased upward and externally rotation during arm elevation, and have limited thoracic extension range of motion and greater kyphotic posture.
However, a previous study found no difference in the scapular kinematics and scapular muscle activation during pull-up in rock climbers with shoulder pain and healthy climbers.
The non-significant finding may be due to that the pure pull-up may not mimic climbing tasks, in which the shoulder and trunk need to adapt different inclination of the wall.
Therefore, the purpose of this study is to investigate the kinematics and muscle activation of the thoracic spine and shoulder in rock climbers with shoulder pain during climbing tasks with different reaching angles.
Methods: Thirty sport climbers with shoulder pain and 30 healthy climbers matched with gender, age, and dominant hand will be recruited in this study.
Testing tasks will include arm elevation in the scapular plane, overhead reaching to the target 15° backward to the frontal plane, pull-up with overhead reaching forward and backward.
Thoracic and shoulder kinematics will be collected using an electromagnetic tracking system.
The upper trapezius, lower trapezius, serratus anterior, latissimus dorsi, and erector spinae were collected with surface electromyography (EMG).
A two-way mixed ANOVA will be used to determine differences between groups in the kinematics and EMG measures at the different arm elevation angles for the testing tasks.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
60
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: YIN-LIANG LIN
- Phone Number: +886-2-28267288
- Email: yllin1020@nycu.edu.tw
Study Contact Backup
- Name: GUAN-XUAN WU
- Email: guanxuan.be11@nycu.edu.tw
Study Locations
-
-
-
Taipei, Taiwan, 112
- Recruiting
- National Yang Ming Chiao Tung University
-
Contact:
- YIN-LIANG LIN
- Phone Number: +886-2-28267288
- Email: yllin1020@nycu.edu.tw
-
Contact:
- GUAN-XUAN WU
- Email: guanxuan.be11@nycu.edu.tw
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Rock climbers with and without shoulder pain
Description
Inclusion Criteria of Patients with Shoulder Pain:
- Ages ranges from 18-40 years old
- At least one year of experience of sport climbing
- Sport Climbing frequency ≥ 6 hours per week in the last one month
- Shoulder pain ≥ 1 month
- Minimum of 3/10 on the numerical rating scale (NRS) in the last one month
Inclusion Criteria of Healthy Subjects in the control group:
- Ages ranges from 18-40 years old
- Gender, age, dominant hand and experience matching to shoulder pain climbers group
- At least one year of experience of sport climbing
- Sport Climbing at least 6 hours per week in the last one month
- No history of shoulder pain in the last six months
Exclusion Criteria of Patients with Shoulder Pain and All Healthy Subjects
- History of upper limb surgery or fracture
- History of shoulder dislocation
- History of neck pain, back pain, or elbow injuries in the last one year
- Wrist or finger pain during sport climbing > 3/10 on the numerical rating scale (NRS)
- Shoulder pain during pull-up > shoulder pain during sport climbing
- Intensive exercise within 12 hours or any delay onset muscle soreness
- Systemic autoimmune disease
- Cancer
- Pregnancy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
rock climbers (healthy group)
Climbers without shoulder pain
|
arm elevation in the scapular plane, overhead reaching to the target 15° backward to the frontal plane, pull-up with overhead reaching forward and backward.
|
rock climbers (shoulder pain group)
Climbers with shoulder pain
|
arm elevation in the scapular plane, overhead reaching to the target 15° backward to the frontal plane, pull-up with overhead reaching forward and backward.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Shoulder kinematics during arm elevation
Time Frame: Immediately during the experiment
|
Scapular kinematics, including anterior/posterior tilt, upward/downward rotation, and internal/external rotation in scapular plane elevation at 30°, 60°, 90°, and 120°, and will be described with degree (°).
|
Immediately during the experiment
|
Scapular muscles activation during arm elevation
Time Frame: Immediately during the experiment
|
The root mean square of electromyography (EMG) data of the upper trapezius, lower trapezius, serratus anterior, and latissimus dorsi will be normalized by the maximum voluntary contraction amplitude (percentage of maximal voluntary contraction, %) and calculated over three 30° increments of motion during arm elevation from 30° to 120°, including 30° - 60°, 60° - 90°, and 90° - 120°.
|
Immediately during the experiment
|
Thoracic kinematics during arm elevation
Time Frame: Immediately during the experiment
|
Thoracic kinematics, including flexion, extension, side flexion and rotation in arm elevation at 30°, 60°, 90°, and 120°, and will be described with degree (°).
|
Immediately during the experiment
|
Shoulder kinematics during pull-up with overhead reaching forward and backward
Time Frame: Immediately during the experiment
|
Scapular kinematics, including anterior/posterior tilt, upward/downward rotation, and internal/external rotation, and will be described with degree (°).
|
Immediately during the experiment
|
Thoracic kinematics during pull-up with overhead reaching forward and backward
Time Frame: Immediately during the experiment
|
Thoracic kinematics, including flexion, extension, side flexion and rotation
|
Immediately during the experiment
|
Trunk muscle activation during arm elevation
Time Frame: Immediately during the experiment
|
The root mean square of electromyography (EMG) data of the erector spinae will be normalized by the maximum voluntary contraction amplitude (percentage of maximal voluntary contraction, %) and calculated over three 30° increments of motion during arm elevation from 30° to 120°, including 30° - 60°, 60° - 90°, and 90° - 120°.
|
Immediately during the experiment
|
Scapular muscles activation during pull-up with overhead reaching forward and backward
Time Frame: Immediately during the experiment
|
The root mean square of electromyography (EMG) data of the upper trapezius, lower trapezius, serratus anterior, and latissimus dorsi will be normalized by the maximum voluntary contraction amplitude (percentage of maximal voluntary contraction, %)
|
Immediately during the experiment
|
Trunk muscle activation during overhead reaching forward and backward.
Time Frame: Immediately during the experiment
|
The root mean square of electromyography (EMG) data of the erector spinae will be normalized by the maximum voluntary contraction amplitude (percentage of maximal voluntary contraction, %)
|
Immediately during the experiment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Thoracic mobility
Time Frame: Immediately during the experiment
|
Range of motion of thoracic spine, described with degree (°).
|
Immediately during the experiment
|
Thoracic kyphosis angle
Time Frame: Immediately during the experiment
|
measured by inclinometers, described with degree (°).
|
Immediately during the experiment
|
Muscle length of pectoralis major
Time Frame: Immediately during the experiment
|
In a supine position with hands behind the head.
A positive (+) indicates muscle tightness, when the elbows cannot touch the testing surface.
|
Immediately during the experiment
|
Muscle length of pectoralis minor
Time Frame: Immediately during the experiment
|
In a supine position, the distance between acromion and testing surface, described with cm.
|
Immediately during the experiment
|
Muscle length of latissimus dorsi
Time Frame: Immediately during the experiment
|
shoulder flexion range of motion in a hook-lying position, described with degree (°)
|
Immediately during the experiment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: YIN-LIANG LIN, National Yang Ming Chiao Tung University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 11, 2023
Primary Completion (Estimated)
June 1, 2024
Study Completion (Estimated)
July 1, 2024
Study Registration Dates
First Submitted
July 11, 2023
First Submitted That Met QC Criteria
July 11, 2023
First Posted (Actual)
July 18, 2023
Study Record Updates
Last Update Posted (Estimated)
November 21, 2023
Last Update Submitted That Met QC Criteria
November 20, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NYCU112095AE
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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