Anterior Knee Pain Syndrome Clinical Trial
Official title:
Evaluation of the Efficacy of Light Therapy for the Treatment of Anterior Knee Pain: A Prospective, Randomized, Double-Blind, Sham-Controlled Clinical Trial
During basic training, 15% of military recruits develop knee pain, which hinders their chance to complete training. Current therapeutic options have had variable levels of success. Light therapy was shown to reduce pain in chronic inflammatory related knee pathology. The current clinical study is designed to evaluate light therapy, as an adjunct to conservative physiotherapy for treatment of acute overuse KP in combat soldiers.
During basic training, 15% of military recruits develop knee pain on the background of
overuse, which hinders their chance to complete training, and leads to high dropout rate with
the accompanying cost to the system. When KP is due to overuse, the time to complete
resolution is typically 2-3 months, but symptoms may last for years. Current therapeutic
options have had variable levels of success. Finding an alternative non-drug, non-invasive
therapeutic modality that is easily incorporated in a field setting and may shorten the
resolution of pain may lead to earlier return to duty thereby reducing the associated cost to
the system and to the individual soldier.
Low-level laser irradiation (LLLI) is non-ionizing and non-thermal, and is within the visible
to near-infrared range of the electromagnetic spectrum. LLLI has been used widely for
alleviation of pain, reduction of inflammation, and acceleration of wound healing.
Pre-clinical and clinical studies have shown that LLLI reduces pain in chronic inflammatory
related knee pathology. However, little is known about the effect of LLLI on acute knee
pathology that account for 25-40% of all knee problems in athletes.
The current study is a prospective, randomized, controlled double blind clinical study
designed to evaluate light therapy, as an adjunct to conservative physiotherapy for treatment
of acute overuse KP in combat soldiers.
The treatment protocol includes conservative physiotherapy and in addition, biweekly sessions
of light therapy or sham irradiation for 4 weeks. Two follow up visits will take place at 1
week and 3 months after the last treatment.
Study evaluations will include physical examination, physical activity tests, subjective pain
level by visual analogue scale, improvement and satisfaction scores, and functional
questionnaires.
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