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The Effect of Laser Therapy in the Management of Adhesive Capsulitis: a Randomized Clinical Trial

N

Necmettin Erbakan University

Status

Not yet enrolling

Conditions

Low Level Laser Therapy
Pain Disorder

Treatments

Other: Low-level laser therapy
Other: High-intensity laser therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT05469672
BOrdahan

Details and patient eligibility

About

In this study, it was aimed to compare the effects of low-level laser therapy (LLLT) and high-intensity laser therapy (HILT) on shoulder joint range of motion, level of pain and functional status in patients with adhesive capsulitis

Full description

This study will be designed as a randomized, prospective, single-blind clinical trial with a 3-week follow-up. A total of 50 patients who applied to our hospital with the complaint of shoulder pain will be evaluated for inclusion in the study. Patients will be randomized into two groups as high-intensity laser (HILT) + stretching exercise group and low-level laser (LLLT) + stretching exercise group.

Enrollment

40 estimated patients

Sex

All

Ages

20 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. patients aged between 25-65 years
  2. patients clinically diagnosed with adhesive capsulitis, characterized by limitation of passive external rotation of the affected shoulder to less than 50% of the contralateral shoulder and normal radiographic finding of the affected shoulder
  3. patients with severe pain and shoulder limitation for at least 3 months
  4. patients who are literate and able to understand verbal instructions in our language.

Exclusion criteria

  1. Calcific tendinopathy, glenohumeral osteoarthritis, fracture, shoulder surgery, shoulder trauma, history of malignancy and infection, history of inflammatory rheumatic diseases
  2. History of bilateral simultaneous adhesive capsulitis
  3. Recent history of lung, breast, or bypass surgery/radiotherapy
  4. History of corticosteroid injection to the same shoulder in the last 1 year
  5. History of cervical radiculopathy/brachial plexus lesion
  6. Neuromuscular disease history
  7. History of physical therapy program for the same shoulder in the last 6 months.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

low-level laser therapy
Active Comparator group
Description:
LLLT will be performed 3 times a week for a period of 3 weeks
Treatment:
Other: Low-level laser therapy
Other: High-intensity laser therapy
high-intensity laser therapy
Active Comparator group
Description:
HILT will be performed 3 times a week for a period of 3 weeks
Treatment:
Other: Low-level laser therapy
Other: High-intensity laser therapy

Trial contacts and locations

0

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Central trial contact

BANU ORDAHAN

Data sourced from clinicaltrials.gov

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