MedPath

The Effect of Scapular Proprioceptive Neuromuscular Facilitation Techniques on Pain and Functionality in Subacromial Impingement Syndrome

Not Applicable
Completed
Conditions
Shoulder Impingement Syndrome
Interventions
Other: Scapular PNF
Other: Exercise program
Registration Number
NCT04273568
Lead Sponsor
Tuğba Akgüller
Brief Summary

The aim of this study was to investigate the effects of scapular proprioceptive neuromuscular facilitation (PNF) techniques applied in addition to exercise therapy in patients with Subacromial impingement syndrome (SIS) on pain, pressure pain threshold (PPT), range of motion (ROM), functionality, scapular dyskinesis, active trigger points and emotional state.

Detailed Description

32 patients between the ages of 20-60 diagnosed with SIS were included in the study.

The patients were randomly divided into two groups. The exercise group received an exercise program of 12 sessions. Scapular PNF techniques were applied to the PNF group with the same exercise program. Patients were evaluated twice; one before and one after 6 weeks of treatment; using Visual Analogue Scale (VAS) for pain, algometer for PPT, digital goniometer for range of motion (ROM), The Disabilities of Arm, Shoulder and Hand (DASH) for functional status, lateral scapular slide test (LSST) for scapular dyskinesis, Travell and Simons criteria for trigger point and Hospital Anxiety and Depression Scale (HADS) for emotional state. At the end of treatment patient satisfaction was evaluated with Global Change Scale.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
32
Inclusion Criteria
  • Aged between 20 and 60
  • Diagnosed with SIS by MRI and clinical examination and a specialist physician
  • Positive impingement tests (Hawkings, Neer and Jobe test) or painful motion arc (60 ° -120 °)
  • Unilateral shoulder pain that has been going on for at least 3 months
  • Signed voluntary consent form
Exclusion Criteria
  • Diagnosed with adhesive capsulitis or massive rotator cuff tear
  • Having undergone upper limb surgery
  • Presence of rheumatological systemic diseases
  • Presence of Glenohumeral instability
  • Having a neurological disease affecting the upper extremity
  • Diagnosed with cervical radiculopathy
  • Degenerative joint disorders
  • Having communication problems
  • Steroid injection therapy or physiotherapy in the past 6 months have been rehabilitated

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Group1 (PNF group)Exercise programScapular PNF and exercise program was applied to the PNF group.
Group 2 (Exercise group)Exercise programExercise program was applied to the exercise group
Group1 (PNF group)Scapular PNFScapular PNF and exercise program was applied to the PNF group.
Primary Outcome Measures
NameTimeMethod
Change from Baseline Functional Status of the patients at 6 weeksBaseline and 6 weeks

The functional status of the patients were evaluated by The Disabilities of the Arm, Shoulder and Hand (DASH). DASH is a scale consisting of 30 questions that question the functional status and symptoms used in musculoskeletal disorders of the upper extremity.The number of Likert scale (1: no difficulty, 5: I can not do at all) is used in answering the questions and the total score obtained is between 0 and 100.

Change from Baseline Pain intensity of the patients at 6 weeksBaseline and 6 weeks

Pain intensity of the patients at rest, during activity and at night was assessed using the VAS; Visual Analog Scale. In this evaluation, individuals were told that the number "0" on the 10 cm long horizontal line expresses "no pain", and the number "10" indicates "unbearable pain" and that individuals should mark their intensity of pain on this line.

Secondary Outcome Measures
NameTimeMethod
Scapular dyskinesisBaseline and 6 weeks

Scapular Dyskinesis was evaluated with "The Lateral Scapular Slide Test (LSKT)". In this test, the distance of the inferior angle of the scapula to the nearest spinous process at 3 different positions (0°, 40-45°, 90°) is measured, and a difference of 1 cm or more between the two sides in any of the three positions is considered positive for scapular dyskinesis.

Active trigger pointsBaseline and 6 weeks

Active 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, middle and posterior group fibers, pectoralis major, pectoralis minor, biceps brachii muscles were evaluated with palpation method in terms of trigger point presence.

Shoulder Range of Motion (ROM)Baseline and 6 weeks

EHA evaluations of flexion, abduction, internal rotation and external rotation of the shoulder joint were performed in the supine position using the digital goniometer.

Pain Pressure Threshold (PPT)Baseline and 6 weeks

Pressure pain threshold was evaluated using the Algometer (dolorimeter).

Emotional stateBaseline and 6 weeks

The 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

Trial Locations

Locations (1)

Istanbul Aydin University

🇹🇷

Istanbul, Turkey

© Copyright 2025. All Rights Reserved by MedPath