Latissimus Dorsi Activation During Shoulder Extension Exercises
Investigation of Latissimus Dorsi Muscle Activation During Shoulder Extension Exercises
1 other identifier
observational
30
1 country
1
Brief 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°). The primary objective is to quantify latissimus dorsi activation and to determine how elevation angle influences activation; secondary analyses compare synergists.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Oct 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 14, 2025
CompletedFirst Submitted
Initial submission to the registry
December 9, 2025
CompletedFirst Posted
Study publicly available on registry
December 22, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2026
CompletedDecember 29, 2025
December 1, 2025
5 months
December 9, 2025
December 22, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (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.
Baseline (Day 1)
Secondary Outcomes (1)
Activity Level
Baseline (Day 1)
Study Arms (1)
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.
Interventions
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.
Eligibility Criteria
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
You may qualify if:
- 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,
You may not qualify if:
- A body mass index greater than 25 kg/m2
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hacettepe University
Ankara, Samandag, 06100, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Irem Duzgun, PhD, Professor
Hacettepe University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor, Department of Physiotherapy and Rehabilitation
Study Record Dates
First Submitted
December 9, 2025
First Posted
December 22, 2025
Study Start
October 14, 2025
Primary Completion
March 1, 2026
Study Completion
March 1, 2026
Last Updated
December 29, 2025
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share
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.