- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07297758
Latissimus Dorsi Activation During Shoulder Extension Exercises
Investigation of Latissimus Dorsi Muscle Activation During Shoulder Extension Exercises
Study Overview
Detailed Description
During shoulder abduction or flexion, narrowing of the subacromial space can lead to subacromial pain syndrome. Weakness or poor coordination of the scapulothoracic and scapulohumeral muscles is among the main causes of subacromial narrowing in individuals with symptomatic rotator cuff tendinopathy. More specifically, insufficient scapular upward rotation and posterior tilt, together with an inadequate ability of the rotator cuff to counter the deltoid's superior pull on the humeral head, may cause impingement of the subacromial soft tissues during overhead dynamic tasks. In young, healthy shoulders, the cranially directed forces that occur during abduction are balanced by co-contraction of the rotator cuff, which prevents superior translation of the humeral head and protects subacromial tissues. When this stabilizing role of the rotator cuff diminishes, the deltoid attempts to compensate; however, this compensation produces a more cranially oriented force, increasing superior migration of the humeral head and the likelihood of subacromial pain.
The latissimus dorsi (LD) originates from the spinous processes of the lower thoracic vertebrae, the thoracolumbar fascia, and the iliac crest, and-together with the teres major-attaches to the medial lip of the intertubercular groove of the humerus. It contributes to shoulder adduction, internal rotation, and extension, and is an important muscle directly linking the upper limb to the trunk. In addition to the rotator cuff, the glenohumeral adductors (pectoralis major and latissimus dorsi) also help limit superior translation of the humeral head; owing to the medio-inferior direction of their tendon force vectors, they act as humeral head depressors. Osteokinematically, the LD can pull the humeral head inferiorly over the glenoid fossa, potentially helping to prevent subacromial impingement.
Various exercises have been recommended for LD rehabilitation, and surface electromyography (sEMG) studies have examined LD activity during movements such as pulldown and pullover. Numerous studies have also sought to determine maximal voluntary isometric contraction (MVIC) of the LD. Prior EMG research indicates that the highest LD MVIC levels are obtained during maximal isometric shoulder extension. A recent study using both surface and fine-wire electrodes also recorded higher LD activation during shoulder extension compared with trunk tasks. Although shoulder extension exercises are widely used at different elevation angles in clinical practice, the effects of performing extension at different angles-particularly on LD activation-have not been clearly delineated. Despite various recommendations for LD rehabilitation, it remains unclear whether different implementations produce different activation profiles, and LD activation during dynamic application of this exercise has not yet been investigated. Therefore, it is important to examine how the highest LD activity obtained during maximal isometric shoulder extension changes when the exercise is performed dynamically. Defining the LD activation profile in dynamic exercise may inform appropriate exercise selection in clinical rehabilitation and help reduce the risk of subacromial impingement.
Aim. To address this gap by examining the level of LD activation during dynamic shoulder extension relative to the reference activity determined by maximal isometric shoulder extension. The study has two specific aims: (1) to determine the EMG activation level of the latissimus dorsi during a shoulder extension exercise, and (2) to investigate the effects of performing shoulder extension at different elevation angles on latissimus dorsi activation.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Irem Duzgun, Professor, PhD
- Phone Number: +90 312-305 15 76
- Email: iremduzgun@hacettepe.edu.tr
Study Contact Backup
- Name: Kubra Caylan Gurses, MSc
- Phone Number: +90 312 305 25 25-186
- Email: kubracaylan@hacettepe.edu.tr
Study Locations
-
-
Samandag
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Ankara, Samandag, Turkey (Türkiye), 06100
- Recruiting
- Hacettepe University
-
Sub-Investigator:
- Gizem Soylu, MSc
-
Sub-Investigator:
- Kubra Caylan Gurses, MSc
-
Contact:
- Irem Duzgun, PhD, Professor
- Phone Number: +90 312-305 15 76
- Email: iremduzgun@hacettepe.edu.tr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age between 18 and 40,
- No restriction of the glenohumeral joint,
- No complaints related to the shoulder, cervical, or lumbar region in the last 6 months,
- No systemic or neurological disease,
- Agreeing to participate in the study,
- A Tegner Activity Score of 5 or higher,
Exclusion Criteria:
- A body mass index greater than 25 kg/m2
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy Active Adults
Ages 18-40; Tegner ≥5; no GH restriction; no shoulder/cervical/lumbar complaints in last 6 months; no systemic/neurologic disease; BMI ≤25 kg/m².
|
Standing with the shoulder in ~30° abduction and external rotation and the elbow extended, participants elevate the arm to three preset flexion angles (30°,60°, 90°, 120°; measured by goniometer) and then perform shoulder extension past the trunk against color-coded elastic bands.
Bands are anchored overhead and pulled diagonally downward; the band angle is adjusted to match each shoulder-flexion condition.
Tempo is metronome-paced: 3 s concentric, 3 s isometric (at peak), 3 s eccentric.
Resistance is individualized using the OMNI Perceived Exertion Scale and titrated until 6-8/10 is reached prior to data capture.
Each condition is recorded for 3 repetitions with ~5 s between reps; ~2 min rest is provided between conditions.
A brief familiarization (~3 min per condition) is given, and the order of MVICs and exercise conditions is randomized.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Electromyography
Time Frame: Baseline (Day 1)
|
Muscle activation will be assessed with an 8-channel surface EMG system (TeleMyo DTS, Noraxon).
Following SENIAM, bipolar Ag/AgCl electrodes (2 cm inter-electrode distance) will be placed over medial and lateral latissimus dorsi, teres major, infraspinatus, posterior deltoid, and triceps brachii, secured with double-sided tape.
Before exercise, MVICs will be obtained on the dominant arm by the same assessor (3 × 5 s with 30 s between trials and 2 min between muscles) using standardized, literature-based positions with verbal encouragement.The exercise protocol will consist of elastic-band resisted shoulder extension performed for three repetitions (3 s concentric-3 s isometric-3 s eccentric) with 5 s between repetitions and 2 min rest between conditions, while EMG from all target muscles is recorded and timing is controlled by a metronome.
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Baseline (Day 1)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Activity Level
Time Frame: Baseline (Day 1)
|
Baseline physical activity will be characterized using the Tegner Activity Scale (0-10) prior to testing; higher scores indicate greater habitual activity.
|
Baseline (Day 1)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Irem Duzgun, PhD, Professor, Hacettepe University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Shoulder-EX-EMG
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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