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The Effectiveness Of Ischemic Compression And IASTM In Trigger Point Treatment In Patients With Rotator Cuff Tear

The Effectiveness Of Ischemic Compression And Instrument Assisted Soft Tissue Mobilization In Trigger Point Treatment In Patients With Rotator Cuff Tear

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04319250
Enrollment
41
Registered
2020-03-24
Start date
2019-02-01
Completion date
2019-08-30
Last updated
2021-03-01

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

Conditions

Rotator Cuff Tears, Shoulder Pain, Myofascial Trigger Point Pain

Keywords

ischemic compression, instrument assisted soft tissue mobilization, trigger point

Brief summary

The aim of this study is to determine the effects of ischemic compression and IASTM techniques on pain, EHA, functionality, anxiety and depression in patients with the diagnosis of RM tear and presence of ATN. In addition, ischemic compression and EDYDM methods were aimed to compare and to reveal which application would be more useful.

Detailed description

In this study participants were randomly divided into two groups. While ischemic compression was applied to one group for the determined active trigger points, instrument assisted soft tissue mobilization (IASTM) was applied to the other group for active trigger points. In addition to the treatment, both groups were subjected to a joint rehabilitation program.

Interventions

ATNs detected in a total of 13 muscles around the shoulder were applied constant pressure at the level of pain tolerated with the thumb (discomfort severity level 7 to 8 out of 10) and for 90 seconds. This method was applied twice a week for 6 weeks.

OTHERIASTM

In order to apply EDYDM in the treatment of ATN, titanium plated stainless steel was divided into two parts, front and back, with two tools. The sweep was applied to the anterior muscle fibers at an angle of 45 ° for 40 seconds. For each TN, continuous pressure was applied with swivel movement at tolerable pain level (discomfort severity level 7 to 8 out of 10) for 1 minute. The back group muscles were applied in the same way.

OTHERRehabilitation Program

A rehabilitation program consisting of exercises and manual therapy used in the conservative treatment of rotator cuff tear for both groups was applied twice a week for 6 weeks.

Sponsors

Istanbul Aydın University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
40 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Being between 40-65 years old * Having been diagnosed with partial RM rupture * RM rupture in MRI image * At least 3 ATNs in the shoulder complex * Hawkins-Kennedy and Empty Can tests positive Symptoms for at least 3 months

Exclusion criteria

* Sensory problems in the back and shoulders, * Shoulder instability * Osteoarthritis in the shoulder joint area * Glenoid or bone fracture * Frozen shoulder pathology * Massive RM rupture * Rheumatological joint problems * Shoulder surgery history

Design outcomes

Primary

MeasureTime frameDescription
Disabilities of the Arm, Shoulder, and Hand Questionnaire (DASH)Change from Baseline at 6 weeksThis is a questionnaire that identifies both functionality and symptoms that can be used in arm, elbow and hand problems. High scores of individuals mean that functional dysfunction is high. Ratings are made between 0 and 100.

Secondary

MeasureTime frameDescription
Global Rating of Change (GRC) scaleAfter 6 weeks treatmentPatient Satisfaction was assessed Global Rating of Change (GRC) scale. The scale used included 5 points (-2: I am much worse. -1: I am worse, 0: I am the same, +1: I am better, +2: I am much better).
Visual Analogue Scale (VAS)Change from Baseline at 6 weeksThe levels of pain felt at rest / activity / night were measured using Visual Analogue Scale (VAS).
Shoulder Range of Motion (ROM)Change from Baseline at 6 weeksEHA evaluations of flexion, abduction, internal rotation and external rotation of the shoulder joint were performed in the supine position using the universal goniometer.
Emotional stateChange from Baseline at 6 weeksThe emotional states of the cases were evaluated using the Hospital Anxiety and Depression Scale (HAD), which consists of 14 questions. (HAD). This scale has a 7-question anxiety (HAD-A) subscale that evaluates the anxiety state, and a 7-question depression (HAD-D) subscale that evaluates the state of depression, and a four-point likert scale is used to answer the questions. For the total score of each sub-score, 0-7 points are normal, 8-10 points are at the border, and 11 points are defined as abnormal
Pain Pressure Threshold (PPT)Change from Baseline at 6 weeksWagner Force One ™ FDIX digital algometer was used to evaluate the pain threshold. Measurements were recorded in kg / cm².
The American Shoulder and Elbow Surgeons Standardized Shoulder Assesment Form (ASES)Change from Baseline at 6 weeksThis score consists of 1 questioning pain and 10 questions questioning daily life activities.The total score is at least 0 and at most 100, and the high scores are positively correlated with the normal function.
Active trigger pointsChange from Baseline at 6 weeksActive trigger points were evaluated by palpation method according to Travell and Simons criteria. Scalene, upper trapezius, levator scapula, supraspinatus, infraspinatus, subskapularis, teres minor, teres major, deltoid anterior and posterior group fibers, pectoralis major, pectoralis minor, biceps brachii muscles were evaluated with palpation method in terms of trigger point presence.

Countries

Turkey (Türkiye)

Outcome results

None listed

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