Low-level Laser Therapy and Static Stretching in Knee Osteoarthritis.

November 6, 2015 updated by: University of Sao Paulo General Hospital

Effect of Low-level Laser Therapy (904 nm) and Static Stretching in Patients With Knee Osteoarthritis: Randomised Controlled Trial.

Osteoarthritis (OA) is a highly prevalent and disabling disease. It is estimated that by 2030 the prevalence of symptomatic OA could reach 30% of the population above 60 years. It is associated with significant morbidity being one of the most common causes of joint pain, functional disability and compromised quality of life. This randomised controlled trial will investigate the effect of low-level laser therapy (LLLT) and static stretching exercises, as monotherapy and in combination, on pain, quality of life, function, mobility, knee range of motion (KROM) and hamstring length in participants with knee OA.

This study will involve 145 people aged 50-75 years with symptomatic radiographic knee OA and will consist of two types of treatments: Low-level laser therapy (LLLT) and stretching exercises. The patients will be randomly allocated to five study groups LLLT active+Stretch, LLLT placebo+Stretch, Stretch, LLLT and Control (with n=29 each). Treatment frequency will be three sessions/week for all active groups. LLLT will involve the use of a Galium-Arsenide laser (904nm, 40 milliwatts, 3 Joules/point, 27 Joules/knee) over 24 sessions for the monotherapy group and 9 sessions for the LLLT+Stretch groups. Stretching will consist of seven exercises completed over 24 sessions. The control group will receive a booklet.

The primary outcome is pain measured by Visual Analogue Scale. Secondary outcomes included quality of life assessed by Western Ontario and McMaster Universities Arthritis Index (WOMAC), function by Lequesne Algofunctional Index, mobility by Timed Up and Go Test (TUG), KROM by goniometry of knee flexion and hamstring shortening by popliteal angle. The statistical method will follow the principles of per-protocol analysis.

Study Overview

Detailed Description

Physical performance as a determinant of disability in osteoarthritis (OA) has been investigated extensively, but research has focused primarily on the effect that the decrease in muscle strength has on the functionality in patients with OA. However, the reduced range of motion in affected joints is also an important risk factor for the occurrence of locomotor disability and other developing disability in patients with OA.

Studies using stretching exercises are scarce in the Reid & Mc Nair (2010) specifically examined the range of motion can be improved in subjects with knee osteoarthritis, although this study did only stretching the hamstrings. The results indicate that there is immediate benefits of stretching in subjects with osteoarthritis of the knee joint, providing evidence for the long term development of stretching programs for this population.

In the literature are observed inconsistent results regarding the benefits of laser treatment in improving pain and function in individuals with knee OA. Also there are few studies that specify which dosage and frequency of laser must be used.

In view of the increasing need to support the role of physiotherapy in evidence-based practice, this study is justified by the need to test the effectiveness of stretching exercises and elucidate the effectiveness of low intensity laser therapy in patients with knee OA.

Study Type

Interventional

Enrollment (Actual)

145

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Sao Paulo
      • Taboao da Serra, Sao Paulo, Brazil, 06775-005
        • Specialized rehabilitation service

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

46 years to 71 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • radiographic evidence of knee osteoarthritis between 2-4 in Kellgren & Lawrence classification
  • pain intensity ≥3 on a 10cm Visual Analogue Scale (VAS)
  • knee symptoms for at least 3 months

Exclusion Criteria:

  • symptomatic hip osteoarthritis
  • any disease where laser treatment is contraindicated (cancer and uncontrolled diabetes mellitus)
  • continuous use of anti-inflammatory drugs
  • other concurrent injury/conditions that will affect their ability to participate in the rehabilitation program and/or assessment procedures.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Factorial Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Stretching
Seven stretching exercises for lower limbs during 24 sessions
7 stretching exercises for lower limbs lasting 30 seconds with 4 repetitions
Experimental: Placebo laser + Stretching
application of placebo laser therapy during nine sessions plus stretching exercises during 24 sessions
7 stretching exercises for lower limbs lasting 30 seconds with 4 repetitions
18 points of application of placebo laser in the knee (frontal faces, lateral and medial)
Other Names:
  • LaserPulse class II IBRAMED
Experimental: Active laser + Stretching
application of active laser therapy during nine sessions plus stretching exercises during 24 sessions
7 stretching exercises for lower limbs lasting 30 seconds with 4 repetitions
18 points of application of active laser in the knee (frontal faces, lateral and medial)
Other Names:
  • LaserPulse (904nm) class II IBRAMED
Experimental: Active Laser
Application of active laser only during 24 sessions
18 points of application of active laser in the knee (frontal faces, lateral and medial)
Other Names:
  • LaserPulse (904nm) class II IBRAMED
No Intervention: Control
Control group that will receive a small book with informations about knee osteoarthritis and postural orientation.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change From Baseline in Visual Analogue Scale for Pain
Time Frame: Baseline and post-intervention, up to 11 weeks
The scale varies from 0 to 10. Higher values represent worse outcomes. The assessment will be done in the patient's first evaluation and after each intervention.
Baseline and post-intervention, up to 11 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change From Baseline in Western Ontario and McMaster Universities Osteoarthritis Index
Time Frame: Baseline and post-intervention, up to 11 weeks
The scale varies from 0 to 96. Higher values represent worse outcomes. The assessment will be done in the patient's first evaluation and after each intervention.
Baseline and post-intervention, up to 11 weeks
Change From Baseline in Range of Motion of Flexion of the Knee
Time Frame: Baseline and post-intervention, up to 11 weeks
Higher values represent better outcomes The assessment will be done in the patient's first evaluation and after each intervention.
Baseline and post-intervention, up to 11 weeks
Change From Baseline in Lequesne Functional Questionnaire
Time Frame: Baseline and post-intervention, up to 11 weeks
The scale varies from 0 to 24. Higher values represent worse outcomes The assessment will be done in the patient's first evaluation and after each intervention.
Baseline and post-intervention, up to 11 weeks
Change From Baseline in Timed Get Up and Go Test
Time Frame: Baseline and post-intervention, up to 11 weeks
Higher values represent worse outcomes The assessment will be done in the patient's first evaluation and after each intervention.
Baseline and post-intervention, up to 11 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

December 1, 2012

Primary Completion (Actual)

December 1, 2014

Study Completion (Actual)

December 1, 2014

Study Registration Dates

First Submitted

August 28, 2012

First Submitted That Met QC Criteria

November 27, 2012

First Posted (Estimate)

November 30, 2012

Study Record Updates

Last Update Posted (Estimate)

December 10, 2015

Last Update Submitted That Met QC Criteria

November 6, 2015

Last Verified

September 1, 2015

More Information

Terms related to this study

Other Study ID Numbers

  • CAPPESQ 455/11

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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