NCT07587931

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

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
8mo left

Started May 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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 Progress1%
May 2026Jan 2027

First Submitted

Initial submission to the registry

April 27, 2026

Completed
17 days until next milestone

First Posted

Study publicly available on registry

May 14, 2026

Completed
6 days until next milestone

Study Start

First participant enrolled

May 20, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 20, 2026

Expected
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 20, 2027

Last Updated

May 14, 2026

Status Verified

May 1, 2026

Enrollment Period

3 months

First QC Date

April 27, 2026

Last Update Submit

May 7, 2026

Conditions

Keywords

Supraspinatus MuscleFull Can ExerciseEccentric ExerciseConcentric ExerciseShoulder RehabilitationMuscle Architecture

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 COMPARATOR

Participants 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.

Other: Concentric Full Can ExerciseOther: Standard Physiotherapy Program

Eccentric Exercise Group

ACTIVE COMPARATOR

Participants 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.

Other: Eccentric Full Can ExerciseOther: Standard Physiotherapy Program

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.

Concentric Exercise Group

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.

Eccentric Exercise Group

Includes therapeutic ultrasound, transcutaneous electrical nerve stimulation (TENS), and standard shoulder rehabilitation exercises applied to all participants.

Concentric Exercise GroupEccentric Exercise Group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Firat University

Elâzığ, MErkez, 23200, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Rotator Cuff Injuries

Condition Hierarchy (Ancestors)

RuptureWounds and InjuriesShoulder InjuriesTendon Injuries

Central Study Contacts

Muharrem Gökhan Beydağı, PhD

CONTACT

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
Model Details: Participants will be randomized into two parallel groups receiving either concentric or eccentric full can exercise in addition to a standard physiotherapy program.
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

Locations