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Comparison of Shoulder Rotation Control, Strength, and Range of Motion During Internal and External Rotation in Individuals With and Without Subacromial Impingement Syndrome

Comparison of Shoulder Rotation Control, Strength, and Range of Motion During Internal and External Rotation in Individuals With and Without Subacromial Impingement Syndrome

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0011303
Enrollment
40
Registered
2025-12-11
Start date
2025-09-01
Completion date
Unknown
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Yonsei University Mirae Campus
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Subacromial impingement syndrome group (1)Participants who show a positive sign on subacromial impingement tests (Neer test and Hawkins test). (2)Individuals who have experienced persistent pain in the anterior, posterior, or lateral aspect of the proximal shoulder for at least one week within the past six months. (3)Participants who report pain during active shoulder elevation. (4)Individuals who present with tenderness upon palpation of the rotator cuff tendons. 2)Non-subacromial impingement syndrome group (1) Participants who do not meet the criteria for the subacromial impingement syndrome group.

Exclusion criteria

Exclusion criteria: *Exclusion Criteria - History of traumatic shoulder injury or shoulder surgery within the past six months - History of shoulder dislocation or subluxation - Diagnosis of adhesive capsulitis or inflammatory arthritis - Individuals who are unable to perform the required measurement tasks

Design outcomes

Primary

MeasureTime frame
olecranon displacement

Secondary

MeasureTime frame
shoulder range of motion;Shoulder rotational strength

Countries

Korea, Republic of

Contacts

Public ContactJu-hee Park

Yonsei University Mirae Campus

qkrtl0817@naver.com+82-33-760-2971

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026