Shoulder and Neck Mobilization in Patients With Subacromial Impingement Syndrome

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorKutahya Health Sciences University

About this trial

Patients who come to Tavşanlı State Hospital's Physical Therapy and Rehabilitation Department and have been diagnosed with subacromial impingement syndrome by a physician will be included. Patients will be selected by randomization method among the patients determined by the physician to receive conservative treatment, shoulder mobilization in addition to conservative treatment, and neck mobilization treatment program in addition to these. Conventional treatments such as hot packs, TENS, ultrasound, and exercise will be given to all patients by the hospital staff. Pain intensity will be evaluated with VAS. Additionally, painful arch and pain-free joint range of motion evaluation will be made using a goniometer. The DASH questionnaire will be used to evaluate shoulder functionality. Sensory evaluation will be made with pressure pain threshold and two-point discrimination tests. Measurements will be made before the intervention and repeated after 3 weeks of intervention.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Being over 18 years of age

Diagnosed with Subacromial Impingement

Not having received any treatment for shoulder problems in the last 6 months

The pain has been continuing for 3 months

Disqualifiers

History of surgery in the shoulder, cervical and thoracic region

Having a shoulder problem such as a frozen shoulder or instability

Full-thickness rotator cuff tear

Having systemic musculoskeletal disease

Trial design

Design model

Parallel

Treatments tested in this trial

  • Conventional Treatment

    Other intervention

    Hot pack,TENS, ultrasound and exercises

  • shoulder mobilization

    Other intervention

    In the glenohumeral joint mobilization technique, distraction, anterior-posterior gliding, and inferior gliding movements will be applied.

  • neck mobilization

    Other intervention

    Bridge, lateral flexion movement combined with traction, anterior-posterior gliding with traction, and lateral gliding techniques will be applied in neck mobilization.

Treatment groups

45 Participants
are divided into 3 treatment groups
Group A: Conventional treatment groupActive comparator 1 intervention
Group B: Conventional treatment + shoulder mobilization groupExperimental treatment 2 interventions
Group C: Conventional treatment + shoulder mobilization + neck mobilization groupExperimental treatment 3 interventions

Trial outcomes

Primary outcomes

1

Pain intensity

Pain intensity will be evaluated with VAS. VAS is a valid and reliable self-report scale consisting of a 10 cm long horizontal line, with scores ranging from 0 (no pain) to 10 (worst pain imaginable). Participants are asked to report the maximum pain they experienced in the last 24 hours. A change of 1.5 points is considered a minimal clinically important difference (MCID) for the VAS.

Time frame
through study completion, an average of 1 year

Secondary outcomes

1

The Arm, Shoulder and Hand Problems (DASH) Questionnaire

(DASH) questionnaire is a questionnaire that evaluates the functional level and disability of the entire upper extremity. At least 27 out of 30 questions must be answered for the inquiry to be evaluated. The query gives a value between 0-100. All questions are scored from 1 to 5. A higher score indicates greater disability.

Time frame
through study completion, an average of 1 year
2

Painful arch assessment

The patient is asked to abduct his arm as much as he can while standing or sitting. The test is positive if the patient feels pain between 60-120° of elevation. The sensitivity of the painful arc test performed in CNS patients was found to be 53% and the specificity was 80%.

Time frame
through study completion, an average of 1 year
3

Painless range of motion assessment

Painless ROM evaluation will be performed in CNS patients due to the presence of a painful arch. Pain-free ROM evaluation includes flexion and abduction movements occurring in the frontal and sagittal planes. These movements are evaluated using a universal goniometer. The patient is asked to actively create 2 movements in a standing or sitting position. While performing measurements with a goniometer, the part with pain-free ROM will be noted in degrees

Time frame
through study completion, an average of 1 year
4

Pressure-pain Threshold Assessment

Pressure pain threshold is the most commonly used method among quantitative sensory tests.Measurements will be taken from the upper trapezius, supraspinatus, and middle deltoideus muscles.

Time frame
through study completion, an average of 1 year

Other outcomes

Sponsors and contacts

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