Adduction and Infraspinatus Activity in Shoulder Pain
ISADER
Isometric Shoulder Adduction During External Rotation Increases Infraspinatus Activity in Adults With and Without Chronic Shoulder Pain: A Randomized Crossover Trial
1 other identifier
interventional
44
1 country
1
Brief Summary
The goal of this randomized crossover trial is to determine whether different levels of shoulder adduction pressure during an external rotation exercise change shoulder muscle activity in adults with chronic shoulder pain and adults without shoulder pain. The main question is whether adding a small amount of shoulder adduction pressure increases activity of the infraspinatus muscle without increasing activity of the deltoid muscles. Researchers will compare three levels of adduction pressure (0, 5, and 10 mmHg) during the same external rotation exercise. Participants will perform the three exercise conditions in a randomly assigned order while researchers measure shoulder muscle activity using surface electromyography.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2023
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
August 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2024
CompletedFirst Submitted
Initial submission to the registry
August 9, 2026
CompletedFirst Posted
Study publicly available on registry
August 14, 2026
CompletedAugust 14, 2026
August 1, 2026
1 year
August 9, 2026
August 12, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Peak Surface Electromyographic Activity of Shoulder Muscles
Peak surface electromyographic activity of the anterior deltoid, middle deltoid, posterior deltoid, infraspinatus, latissimus dorsi, and middle trapezius during the shoulder external rotation exercise. Electromyographic activity was normalized to the maximum voluntary isometric contraction (MVIC) and expressed as a percentage of MVIC.
Day 1. During each experimental condition (0, 5, and 10 mmHg)
Study Arms (6)
Sequence 1: 0-5-10 mmHg
EXPERIMENTALParticipants assigned to this sequence performed the shoulder external rotation exercise under 0 mmHg, 5 mmHg, and 10 mmHg of shoulder adduction pressure, respectively.
Sequence 2: 0-10-5 mmHg
EXPERIMENTALParticipants assigned to this sequence performed the shoulder external rotation exercise under 0 mmHg, 10 mmHg, and 5 mmHg of shoulder adduction pressure, respectively.
Sequence 3: 5-0-10 mmHg
EXPERIMENTALParticipants assigned to this sequence performed the shoulder external rotation exercise under 5 mmHg, 0 mmHg, and 10 mmHg of shoulder adduction pressure, respectively.
Sequence 4: 5-10-0 mmHg
EXPERIMENTALParticipants assigned to this sequence performed the shoulder external rotation exercise under 5 mmHg, 10 mmHg, and 0 mmHg of shoulder adduction pressure, respectively.
Sequence 5: 10-0-5 mmHg
EXPERIMENTALParticipants assigned to this sequence performed the shoulder external rotation exercise under 10 mmHg, 0 mmHg, and 5 mmHg of shoulder adduction pressure, respectively.
Sequence 6: 10-5-0 mmHg
EXPERIMENTALParticipants assigned to this sequence performed the shoulder external rotation exercise under 10 mmHg, 5 mmHg, and 0 mmHg of shoulder adduction pressure, respectively.
Interventions
Participants performed the shoulder external rotation exercise while maintaining 0 mmHg of isometric shoulder adduction pressure against a biofeedback wedge. The exercise was performed with the shoulder positioned at approximately 45 degrees of external rotation from 0 degrees of glenohumeral rotation.
Participants performed the shoulder external rotation exercise while maintaining 5 mmHg of isometric shoulder adduction pressure against a biofeedback wedge. The exercise was performed with the shoulder positioned at approximately 45 degrees of external rotation from 0 degrees of glenohumeral rotation.
Participants performed the shoulder external rotation exercise while maintaining 10 mmHg of isometric shoulder adduction pressure against a biofeedback wedge. The exercise was performed with the shoulder positioned at approximately 45 degrees of external rotation from 0 degrees of glenohumeral rotation.
Eligibility Criteria
You may qualify if:
- Shoulder Pain Group (SPG):
- Adults aged 18 years or older.
- Medical diagnosis of chronic non-traumatic shoulder pain lasting more than 3 months.
- Resting pain intensity of at least 2 cm on a visual analogue scale (VAS).
- Ability to perform at least 130° of shoulder flexion, 90° of shoulder abduction, and 45° of shoulder external rotation.
- Pain-Free Group (PFG):
- Adults aged 18 years or older.
- No current shoulder or neck symptoms.
- No shoulder or neck symptoms during the previous 2 years.
- No previous medical consultation for shoulder or neck discomfort.
- Full shoulder abduction and external rotation range of motion.
- Ability to perform pain-free maximal isometric contractions during shoulder abduction and external rotation.
You may not qualify if:
- Shoulder Pain Group (SPG):
- History of neck or upper limb surgery.
- History of glenohumeral instability or upper limb fracture.
- Neck pain or pain in another segment of the upper limb.
- Systemic diseases that could influence shoulder movement or muscle activation, including rheumatoid arthritis or neuromuscular diseases.
- Physical therapy treatment during the previous year for pain in the affected upper limb.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Universidad de La Frontera
Temuco, La Araucanía, Chile
Related Publications (1)
Bascour-Sandoval, Claudio, Gajardo-Burgos, Rubén, Gálvez-García, Germán, & Barramuño-Medina, Mauricio. (2021). Effect of Adduction During Glenohumeral External Rotation Exercises in the Scapulohumeral Muscles. International Journal of Morphology, 39(5), 1316-1322. https://dx.doi.org/10.4067/S0717-95022021000501316
BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Germán Gálvez García, PhD
Universidad de La Frontera
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Doctor
Study Record Dates
First Submitted
August 9, 2026
First Posted
August 14, 2026
Study Start
August 1, 2023
Primary Completion
August 1, 2024
Study Completion
August 1, 2024
Last Updated
August 14, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP
- Time Frame
- The individual participant data and supporting information will become available beginning 12 months after publication of the study results and will remain available for 5 years.
- Access Criteria
- Data will be available to qualified researchers who submit a scientifically sound research proposal for analyses that are consistent with the purpose of the original study. Requests will be reviewed by the study investigators. Access will be provided following approval of the request and completion of an appropriate data use agreement, where applicable. Researchers will be required to comply with applicable ethical, confidentiality, and data protection requirements.
Deidentified individual participant data underlying the published results will be shared, including participant-level surface electromyography data and relevant demographic and clinical variables. A data dictionary describing the shared variables will also be provided. Data will be shared in a format that allows appropriate secondary analyses while protecting participant confidentiality.