Muscle ActivationNCT07297758
Latissimus Dorsi Activation During Shoulder Extension Exercises
An observational study of Muscle Activation, run by Hacettepe University at 1 site in Turkey (Türkiye).
Trial summary
This observational, cross-sectional laboratory study at Hacettepe University will examine surface EMG activation of the latissimus dorsi during resisted, dynamic shoulder extension performed at three shoulder flexion angles (30°,60°, 90°, 120°). Read more about this study
- Who is it for?
- Ages 18 to 40 yearsHealthy volunteers can take part
- Conditions the study is for
- Muscle Activation
- What is being tested?
- Exercise
- Type of treatment
- Lifestyle or therapy programme
- How many people
- 31 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 14 Oct 2025to 1 Apr 2026
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 40 years
- All sexes
- Healthy volunteers accepted
- Adult
Study population: Healthy, physically active adults aged 18-40 years, recruited from a university cohort and local community, for a single-visit laboratory EMG study at Hacettepe University. Eligibility requires Tegner ≥5, full glenohumeral range of motion, no shoulder/cervical/lumbar complaints in the past 6 months, and no systemic or neurological disease; individuals with BMI >25 kg/m² are excluded
Who may be able to join
- 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,
Who cannot join
- A body mass index greater than 25 kg/m2
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Investigation of Latissimus Dorsi Muscle Activation During Shoulder Extension Exercises
This observational, cross-sectional laboratory study at Hacettepe University will examine surface EMG activation of the latissimus dorsi during resisted, dynamic shoulder extension performed at three shoulder flexion angles (30°,60°, 90°, 120°). The primary objective is to quantify latissimus dorsi activation and to determine how elevation angle influences activation; secondary analyses compare synergists.
Read the 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.
- Conditions
- Muscle Activation
- Being tested
- Exercise
- Keywords
- Shoulder, Latissimus Dorsi, Exercise
- Medical subject headings
- Motor Activity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ExerciseBehavioural
Standing with the shoulder in ~30° abduction and neutral 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. Within each angle condition, the band and grip length were kept constant across the three repetitions, and participants maintained the marked starting hand position at a horizontal distance of 120 cm from the band anchor. 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.
| Study group | Role | What they receive |
|---|---|---|
| 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. Receives: Behavioral: Exercise |
What is being measured
The primary outcome is the main question the study is designed to answer.
Electromyography
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.
Measured: Baseline (Day 1)
Secondary outcomes (1)
Activity Level
Baseline physical activity will be characterized using the Tegner Activity Scale (0-10) prior to testing; higher scores indicate greater habitual activity.
Measured: Baseline (Day 1)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Dec 2025
- Study start14 Oct 2025
- Primary completion1 Feb 2026
- Study completion1 Apr 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Muscle ActivationStudies of the same condition, open and under way.
- More trials run by Hacettepe UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Cross-sectional
- Enrolment
- 31 participants (actual)
Sponsor and investigators
- Lead sponsor
- Hacettepe University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Irem Duzgun, Hacettepe University
- Investigators
- Irem Duzgun, PhD, Professor, Principal investigator, Hacettepe University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07297758
- Sponsor's protocol ID
- Shoulder-EX-EMG
- Status last verified
- Dec 2025
- First submitted
- 9 Dec 2025
- Last updated
- 26 Oct 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: No individual participant data (IPD) will be shared. De-identified aggregate results will be disseminated in publications. The dataset includes physiological signals; synchronized videos are deleted after analysis.
Study at a glance
From the registry record, last updated by the sponsor on 26 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Investigation of Latissimus Dorsi Muscle Activation During Shoulder Extension Exercises
- ClinicalTrials.gov ID
- NCT07297758
- Acronym / sponsor ID
- Shoulder-EX-EMG
- Conditions
- Muscle Activation
- Keywords
- Shoulder, Latissimus Dorsi, Exercise
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 31 participants (actual)
- Lead sponsor
- Hacettepe UniversityUniversity, hospital or other
- Study start
- 14 Oct 2025 (actual)
- Primary completion
- 1 Feb 2026 (actual)
- Study completion
- 1 Apr 2026 (actual)
- First posted
- 22 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This observational, cross-sectional laboratory study at Hacettepe University will examine surface EMG activation of the latissimus dorsi during resisted, dynamic shoulder extension performed at three shoulder flexion angles (30°,60°, 90°, 120°). The primary objective is to quantify latissimus dorsi activation and to determine how elevation angle influences activation; secondary analyses compare synergists.
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 design
- Observational model
- Other
- Time perspective
- Cross-sectional
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Healthy Active Adults | – | Behavioral: ExerciseAges 18-40; Tegner ≥5; no GH restriction; no shoulder/cervical/lumbar complaints in last 6 months; no systemic/neurologic disease; BMI ≤25 kg/m². |
Who may qualify
- Ages
- 18 to 40 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- Healthy, physically active adults aged 18-40 years, recruited from a university cohort and local community, for a single-visit laboratory EMG study at Hacettepe University. Eligibility requires Tegner ≥5, full glenohumeral range of motion, no shoulder/cervical/lumbar complaints in the past 6 months, and no systemic or neurological disease; individuals with BMI >25 kg/m² are excluded
Key inclusion criteria (6 listed)
- 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,
Key exclusion criteria (1 listed)
- A body mass index greater than 25 kg/m2
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ExerciseStanding with the shoulder in ~30° abduction and neutral 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. Within each angle condition, the band and grip length were kept constant across the three repetitions, and participants maintained the marked starting hand position at a horizontal distance of 120 cm from the band anchor. 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. | Behavioural | Healthy Active Adults |
Primary outcome
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.
1 secondary outcome
Activity Level
Time frame: Baseline (Day 1)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Oct 2026.
- Individual participant dataSharing planned: No. No individual participant data (IPD) will be shared. De-identified aggregate results will be disseminated in publications. The dataset includes physiological signals; synchronized videos are deleted after analysis.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Irem Duzgun, PhD, Professor principal investigator
Hacettepe University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Muscle Activation, run by Hacettepe University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 26 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Electromyography (time frame: Baseline (Day 1)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Oct 2026.