Concentric vs Eccentric Full Can Exercise in Partial Rotator Cuff Tears
FULLCAN-PRCT
Comparison of the Effects of Concentric and Eccentric Full Can Exercises on Supraspinatus Muscle Architecture in Individuals With Partial Rotator Cuff Tears
1 other identifier
interventional
60
1 country
1
Brief Summary
This study aims to compare the effects of concentric and eccentric full can exercises on supraspinatus muscle architecture in individuals with partial rotator cuff tears. Rotator cuff tears are a common cause of shoulder pain and functional limitation. The supraspinatus muscle plays a key role in shoulder movement and stability, and its structure may be affected in individuals with partial tears. Exercise-based rehabilitation is widely used in the conservative management of these conditions. The full can exercise is commonly prescribed to selectively activate the supraspinatus muscle. However, the effects of different contraction types, specifically concentric and eccentric exercises, on muscle structure and clinical outcomes are not fully understood. In this study, participants will be randomly assigned to either a concentric or eccentric full can exercise group. Both groups will receive a standard physiotherapy program, including therapeutic ultrasound and transcutaneous electrical nerve stimulation (TENS), in addition to the assigned exercise protocol. The intervention will last for 6 weeks, with sessions performed three times per week. Outcomes will be assessed before and after the intervention. The primary outcome is the change in supraspinatus muscle pennation angle measured by ultrasound imaging. Secondary outcomes include muscle architecture parameters, pain intensity, range of motion, muscle strength, functional status, and kinesiophobia. The findings of this study may help improve exercise selection in the rehabilitation of individuals with rotator cuff tears.
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 May 2026
Shorter than P25 for not_applicable
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
First Submitted
Initial submission to the registry
April 27, 2026
CompletedFirst Posted
Study publicly available on registry
May 14, 2026
CompletedStudy Start
First participant enrolled
May 20, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 20, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 20, 2027
May 14, 2026
May 1, 2026
3 months
April 27, 2026
May 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Supraspinatus Muscle Pennation Angle
The pennation angle of the supraspinatus muscle will be measured using B-mode ultrasonography. Measurements will be obtained at baseline (T0) and after 6 weeks (T1). The change between time points will be analyzed. Supraspinatus Muscle Pennation Angle: * Assessed by B-mode ultrasonography. * Pennation angle will be measured in degrees (°). * Higher values indicate greater muscle architectural adaptation. * Measured at baseline (T0) and after 6 weeks of intervention (T1).
Baseline and 6 weeks
Secondary Outcomes (8)
Change in Supraspinatus Muscle Fiber Length
Baseline and 6 weeks
Change in Physiological Cross-Sectional Area of Supraspinatus
Baseline and 6 weeks
Change in Pain Intensity (VAS)
Baseline and 6 weeks
Change in Shoulder Range of Motion
Baseline and 6 weeks
Change in Shoulder Muscle Strength
Baseline and 6 weeks
- +3 more secondary outcomes
Study Arms (2)
Concentric Exercise Group
ACTIVE COMPARATORParticipants will receive a standard physiotherapy program including ultrasound, TENS, and shoulder rehabilitation exercises, combined with concentric full can exercises. The concentric phase (lifting) will be emphasized, while the eccentric phase will be minimally loaded.
Eccentric Exercise Group
ACTIVE COMPARATORParticipants will receive a standard physiotherapy program including ultrasound, TENS, and shoulder rehabilitation exercises, combined with eccentric full can exercises. The eccentric phase (lowering) will be emphasized, while the concentric phase will be minimally loaded.
Interventions
A strengthening exercise performed in the scapular plane with emphasis on the eccentric phase. The lowering phase is performed slowly in approximately 4 seconds against resistance, while the concentric phase is minimized. Exercises are performed 3 times per week for 6 weeks.
A strengthening exercise performed in the scapular plane with emphasis on the eccentric phase. The lowering phase is performed slowly in approximately 4 seconds against resistance, while the concentric phase is minimized. Exercises are performed 3 times per week for 6 weeks.
Includes therapeutic ultrasound, transcutaneous electrical nerve stimulation (TENS), and standard shoulder rehabilitation exercises applied to all participants.
Eligibility Criteria
You may qualify if:
- Aged between 18 and 65 years
- Diagnosed with partial supraspinatus tendon tear confirmed by ultrasound or magnetic resonance imaging
- Shoulder pain lasting at least 3 months
- Pain intensity ≥3 on the Visual Analog Scale (VAS)
- Willing to participate and provide informed consent
You may not qualify if:
- Full-thickness rotator cuff tear
- History of shoulder surgery
- Shoulder instability
- Neurological disorders
- Rheumatological diseases
- Corticosteroid injection within the last 3 months
- Inability to adhere to the exercise program
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Firat Universitylead
- Elazıg Fethi Sekin Sehir Hastanesicollaborator
Study Sites (1)
Firat University
Elâzığ, MErkez, 23200, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- Outcome assessments will be performed by a physiotherapist who is blinded to group allocation. Participants and care providers will not be blinded due to the nature of the exercise interventions.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor, PhD
Study Record Dates
First Submitted
April 27, 2026
First Posted
May 14, 2026
Study Start
May 20, 2026
Primary Completion (Estimated)
August 20, 2026
Study Completion (Estimated)
January 20, 2027
Last Updated
May 14, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share