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

T

Tuğba Akgüller

Status

Completed

Conditions

Shoulder Impingement Syndrome

Treatments

Other: Scapular PNF
Other: Exercise program

Study type

Interventional

Funder types

Other

Identifiers

NCT04273568
tugbaakguller

Details and patient eligibility

About

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.

Full 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.

Enrollment

32 patients

Sex

All

Ages

20 to 60 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

32 participants in 2 patient groups

Group1 (PNF group)
Experimental group
Description:
Scapular PNF and exercise program was applied to the PNF group.
Treatment:
Other: Exercise program
Other: Scapular PNF
Group 2 (Exercise group)
Active Comparator group
Description:
Exercise program was applied to the exercise group
Treatment:
Other: Exercise program

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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