Laser Therapy in Adhesive Capsulitis

Sponsor
Hitit University (Other)
Overall Status
Completed
CT.gov ID
NCT03929276
Collaborator
(none)
31
1
3
5
6.2

Study Details

Study Description

Brief Summary

Adhesive capsulitis is an idiopathic disease characterized by a decrease in the volume of the glenoid capsule, the development of fibrosis and a progressive decrease in the range of joint movement with pain. Shoulder pain and stiffness are accompanied by disability. The purpose of the study is to evaluate and compare the effects of high-intensity laser therapy on pain, disease - related disability and quality of life in patients with shoulder restriction and pain due to adhesive capsulitis.

Condition or Disease Intervention/Treatment Phase
  • Device: high-intensity laser therapy & exercises
  • Device: Shame laser & exercises
  • Other: exercise
N/A

Detailed Description

Adhesive capsulitis is an idiopathic disease characterized by a decrease in the volume of the glenoid capsule, the development of fibrosis and a progressive decrease in the range of joint movement with pain. Shoulder pain and stiffness are accompanied by disability. It is thought that the incidence is 3% to 5% in the general population and 20% in people with diabetes. Although usually reported to be self-limiting in 2 to 3 years, studies have reported that 40% of patients have persistent pain and stiffness for more than 3 years.

Therefore, various therapies are used to reduce pain and increase the range of motion more rapidly without waiting for spontaneous recovery. Adhesive capsulitis treatment includes conservative and surgical treatment options. The options for non-surgical treatments are pharmacological treatments including intra-articular injection and physical therapy modalities. As for physical therapy modalities, various interventions are used. These include heat or ice, therapeutic ultrasound, transcutaneous electrical nerve stimulation and laser therapies.

The aim of exercise programs consisting of joint range of motion (ROM), strengthening and stretching exercises, proprioceptive neuromuscular facilitation and mobilization techniques is to alleviate pain caused by the capsular contracture and to improve glenohumeral ROM.

The purpose of the study is to evaluate and compare the effects of high-intensity laser therapy on pain, disease - related disability and quality of life in patients with shoulder restriction and pain due to adhesive capsulitis.

Study Design

Study Type:
Interventional
Actual Enrollment :
31 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Efficacy of High-intensity Laser Therapy in Patients With Adhesive Capsulitis
Actual Study Start Date :
Apr 22, 2019
Actual Primary Completion Date :
Sep 22, 2019
Actual Study Completion Date :
Sep 22, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: high-intensity laser therapy & exercises

High-intensity laser therapy application with iLux Laser device + exercise program

Device: high-intensity laser therapy & exercises
A total of 15 sessions of high-dose laser treatment- i Lux Laser (Mectronic Medicale, Italy)- (in the first phase, 8 Watt for the analgesic effect; in the second phase, 12 Watt in burst mode for the biostimulation effect; and finally in the third phase with 8 Watt) will be applied.

Other: exercise
Therapeutic exercises All participants received 25-minutes of passive stretching, active assisted range of motion and codman pendicular exercises (10 repetitions, 3 sets, 3-minutes rest between sets) to the shoulder joint, supervised by the same physiotherapist five times a week for 3 weeks.

Placebo Comparator: Shame laser & exercises

Sham high-intensity laser therapy application with iLux Laser device + exercise program

Device: Shame laser & exercises
Sham laser treatment (the same device to be used, 0 watts) will be given.

Other: exercise
Therapeutic exercises All participants received 25-minutes of passive stretching, active assisted range of motion and codman pendicular exercises (10 repetitions, 3 sets, 3-minutes rest between sets) to the shoulder joint, supervised by the same physiotherapist five times a week for 3 weeks.

Active Comparator: control - exercises only group

exercise program

Other: exercise
Therapeutic exercises All participants received 25-minutes of passive stretching, active assisted range of motion and codman pendicular exercises (10 repetitions, 3 sets, 3-minutes rest between sets) to the shoulder joint, supervised by the same physiotherapist five times a week for 3 weeks.

Outcome Measures

Primary Outcome Measures

  1. Visual analogue scale for pain (VAS- pain) [2 weeks]

    Pain intensity was measured with visual analogue scale for pain (0-10 mm; 0 means no pain, 10 means severe pain) which is used to measure musculoskeletal pain with very good reliability and validity.

Secondary Outcome Measures

  1. Shoulder pain and disability index [2 weeks]

    It is a self-administered questionnaire and two dimensions are measured, one for pain and the other for functional activities. Scores range from 0 to 100 with scores closer to 0 indicating lower (or no) disability and scores closer to 100 indicating greater disability.

  2. Short Form Health Survey 36 (SF-36) [2 weeks]

    Short- form health survey 36 contains 36 items which are used to evaluate the quality of life of patients with chronic pain. It measures eight different domains that address physical functioning, physical role limitation, pain, general health, vitality, social functioning, emotional role limitation and mental health. The score of each domain ranges from 0 (worse quality of life) to 100 (best quality of life).

  3. Range of motion of shoulder joint measurements [2 weeks]

    shoulder flexion, abduction, external rotation and internal rotation

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Subjects with adhesive capsulitis diagnosis by physical examination (Compared with intact side, there is more than 25% limitation in at least two directions of shoulder range of motion)

  • Subjects have complaints for at least 1 month

  • No pregnancy / breastfeeding

Exclusion Criteria:
  • History of bilateral adhesive capsulitis

  • History of shoulder trauma, fracture, shoulder shoulder surgery, calcific tendinopathy, glenohumeral osteoarthritis, inflammatory rheumatic diseases, tumor, infection

  • History of corticosteroid injection in the shoulder during the last 3 months

  • History of recent lung, breast or bypass surgery

  • History of cervical radiculopathy / brachial plexus lesion

  • History of neuromuscular disease

  • History of physical therapy program for the same shoulder in the last 6 months

Contacts and Locations

Locations

Site City State Country Postal Code
1 Tuğba Atan Corum Turkey 19100

Sponsors and Collaborators

  • Hitit University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Tuğba Atan, Assoc. Prof., Hitit University
ClinicalTrials.gov Identifier:
NCT03929276
Other Study ID Numbers:
  • 19-KAEK-061
First Posted:
Apr 26, 2019
Last Update Posted:
Apr 28, 2020
Last Verified:
Apr 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Tuğba Atan, Assoc. Prof., Hitit University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 28, 2020