Skip to content

Effects of Myofascial Chain Tension Modulation Combined With Scapular Corrective Exercise on Scapular Movement Performance and Functional Outcomes in Tennis Players With Subacromial Impingement Syndrome

Effects of Myofascial Chain Tension Modulation Combined With Scapular Corrective Exercise on Scapular Movement Performance and Functional Outcomes in Tennis Players With Subacromial Impingement Syndrome

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07385378
Enrollment
36
Registered
2026-02-04
Start date
2026-02-01
Completion date
2027-08-31
Last updated
2026-02-04

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

Conditions

Subacromial Impingement Syndrome

Keywords

muscle imbalance, scapular dyskinesis, instrument-assisted soft tissue mobilization

Brief summary

Subacromial Impingement Syndrome (SIS) is characterized by abnormal scapular motion, including decreased upward rotation, increased internal rotation, and excessive anterior tilting, which impair shoulder and arm function. Integrated scapular rehabilitation combines Instrument-Assisted Soft Tissue Mobilization (IASTM) and postural correction exercises. IASTM detects soft tissue restrictions through multidirectional strokes and enhances the pain threshold of myofascial trigger points (MTrPs) via reflex hyperemia. Postural correction exercises aim to strengthen weakened muscles and stretch tight ones to improve stability and posture. The combination of these interventions may enhance scapular stability and dynamic control. This study aimed to investigate the effects of integrated scapular rehabilitation on scapular kinematics, movement correction, functional improvement, and pain management in tennis athletes with SIS. A two-way repeated-measures ANOVA was used to analyze pre- and post-intervention effects.

Detailed description

Participants aged 20 years or older were recruited. Outcome measures included pain intensity, Shoulder Pain and Disability Index (SPADI), shoulder range of motion (flexion, abduction, internal and external rotation), modified Scapular Assistance Test (mSAT), muscle strength (upper, middle, and lower trapezius; serratus anterior; rhomboids; levator scapulae; internal and external rotators), soft tissue elasticity (upper trapezius), myofascial trigger point pain threshold (upper trapezius, pectoralis minor, levator scapulae, rhomboids), subacromial space, and supraspinatus thickness.

Interventions

IASTM is an assistive instrument designed to reduce the physical effort required by the practitioner and can be applied without a specific directional pattern. It aims to induce localized reactive hyperemia through repeated application, temporarily alter tissue rheological properties, and modulate sensory feedback via cutaneous mechanoreceptors. Its mechanisms involve both mechanical and neurophysiological components.

Elastic resistance bands of different colors were used for resistance training, with training intensity increased or decreased by selecting bands of varying resistance levels.

Sponsors

China Medical University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
20 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Participants were included if they met all of the following conditions: 1. a VAS score greater than 3 during the Hawkins test (indicating mild to moderate pain), 2. at least two positive results among the Hawkins test, Neer test, and painful arch test, and 3. a positive result on the mSAT. Only participants who fulfilled all three criteria were enrolled in the study.

Exclusion criteria

* Participants were excluded if they had a history of clavicle, scapular, or humeral fractures; shoulder dislocation; or rotator cuff surgery; positive results on the cervical compression test, apprehension test, or drop arm test; had received corticosteroid injections within the past three months; had undergone physical therapy within the past six months; or reported a VAS score higher than 9.

Design outcomes

Primary

MeasureTime frame
Pain (VAS score during the Hawkins test)Participants were assessed at time points: prior to the intervention (baseline), immediately three weeks after the intervention, and at a one-month follow-up.

Contacts

CONTACTYueh-Ling Hsieh, PHD
sherrie@mail.cmu.edu.tw04-22053366
CONTACTYu-Wei Lee
will860619@gmail.com0972141913

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026