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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).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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
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.

Turkey (Türkiye)1 site
  • Hacettepe University

    Ankara, Samandag, 06100

Other trials in Turkey (Türkiye)

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.

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 groups in NCT07297758
Study groupRoleWhat they receive
Healthy Active AdultsAges 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.

  1. 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)
  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.

  1. First posted22 Dec 2025
  2. Study start14 Oct 2025
  3. Primary completion1 Feb 2026
  4. Study completion1 Apr 2026

Resources

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)
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.

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.

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