High and Low Laser for Subacromial Impingement Syndrome

Not Applicable

Completed

• Conditions: Subacromial Impingement Syndrome
• Interventions: Other: traditional physical therapy exercises; Other: high intensity laser in addition to traditional physical therapy exercises; Other: low level laser in addition to traditional physical therapy exercises

• Registration Number: NCT04784377
• Lead Sponsor: Cairo University

Brief Summary

Shoulder pain is the third most common musculoskeletal problem after lumbar and neck diseases in clinical practice, and the most common cause of shoulder pain is subacromial impingement syndrome. The main goal of treatment is to reduce pain and to solve the mechanical problem that causes functional impairment. Low-level laser treatment is an increasingly used treatment modality in the treatment of subacromial impingement syndrome as in many musculoskeletal diseases, as it promotes cell proliferation and tissue regeneration by its anti-inflammatory and photobiostimulation properties. Also, High-intensity laser therapy is a treatment method that is gaining popularity in the recent years. These ultra-short impulses effect a deep action in the biological tissue (3-4 cm), with a homogeneous distribution of the light source in the irradiated soft tissue, but without excessive thermal enhancements. It reduces pain and edema with photomechanic effects in deep tissues. As far as the investigators know, there are no studies comparing these two treatment modalities in subacromial impingement syndrome yet. This study was planned to compare the efficacy of High-intensity laser therapy and low-intensity laser therapy in treatment of patients with subacromial impingement syndrome.

Detailed Description

Not available

Study Timeline

• Status Verified: 2021-03
• Study First Submitted: 2021-03-02
• Study First Submitted QC: 2021-03-02
• Study First Posted: 2021-03-05
• Study Start: 2021-03-15
• Primary Completion: 2022-08-15
• Study Completion: 2022-09-15
• Last Update Submitted: 2023-01-21
• Last Update Posted: 2023-01-25

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 42

Inclusion Criteria

• shoulder pain for at least one month
• male and female patients with age range from 25-45 years old
• positive impingement test results
• stage I or II disease according to the Neer classification, confirmed by MRI
• visual analog scale score greater than 40 mm.

Exclusion Criteria

patients will be excluded if they have:

• major trauma to the shoulder
• stage III subacromial impingement syndrome
• diabetes mellitus
• hypothyroidism
• calcific tendinitis
• adhesive capsulitis (forward flexion less than 160, horizontal abduction less than 160
• installation of cardiac pacemaker
• history of a physical therapy program for the same shoulder in the last 6 months.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
control group	traditional physical therapy exercises	-
High laser group	high intensity laser in addition to traditional physical therapy exercises	-
low laser group	low level laser in addition to traditional physical therapy exercises	-

Primary Outcome Measures

Name	Time	Method
pain intensity	change from base line at three weeks	Pain will be evaluated by a visual analogue scale (VAS). The patient will be asked to mark the severity of pain on a 100-mm line with "no pain" on one end and "most unbearable pain" on the other end

Secondary Outcome Measures

Name	Time	Method
Pittsburgh Sleep Quality Index (PSQI)	change from baseline at three weeks	This scale assesses sleep quality and disorder and consists of seven subcomponents (subjective sleep quality, sleep latency, sleep duration, sleep efficiency, sleep disturbance, drug use, and daytime functions) and 19 items. Each component is evaluated on a score of 0-3 and is evaluated with a total sleep score ranging from 0 to 21, and high scores represent low sleep quality. A PSQI total score \< 5 points is considered "good" sleep quality and \> 5 points is "bad" sleep quality.
pain pressure threshold	change from baseline at three weeks	Pressure Pain Threshold will be determined with an analogue algometer at the most painful point of the subacromial area. This point will be determined by a previous examination based on the point that the patient determined as 'his or her point of maximum pain'.
shoulder range of motion	change from baseline at three weeks	Flexion, abduction, and external rotation will be measured by using goniometer in a supine position and the active movements will be recorded. The goniometer will be centered at the acromion for abduction, greater tubercle for flexion, and olecranon for external rotation at 90° shoulder and elbow flexion
Shoulder Pain and Disability Index	change from baseline at three weeks	this scale will be used to assess functional status of the shoulder. The SPADI includes shoulder questions and consists of two subscales: pain and disability. Pain subscale consists of 5 items, and disability subscale consists of 8 items, and the total score is 0-100

Trial Locations

Locations (1)

Faculty of Physical Therapy, Cairo University; 🇪🇬 Giza, Egypt