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临床试验/NCT02665507
NCT02665507已完成2 期

Evaluation of the Efficacy of Light Therapy for the Treatment of Back Pain in Pilots

Hebrew University of Jerusalem1 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2018年3月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
42
试验地点
1
主要终点
Time to reach minimal important change in pain level by visual analog scale (VAS)

研究概览

简要总结

Back pain is a common complaint among pilots. Current treatments include physiotherapy and chiropractic manipulations. Low-level laser irradiation (LLLI) in the visible to near-infrared range was shown to reduce neck and low back pain.

The purpose of the study is to evaluate the efficacy of Light Therapy for treatment of back pain in pilots.

详细描述

Background: Lumbar spine disorders are common conditions in pilots of various aircraft with etiology related to sub-optimal ergonomics, exposure to G-forces, the weight of the head gear and exposure to extensive vibrations. Current treatments include physiotherapy and chiropractic manipulations. Low-level laser irradiation (LLLI) is a non-ionizing, non-thermal irradiation within the visible to near infrared range of the light spectrum. LLLI has been used widely for alleviation of pain in inflammatory processes and acceleration of wound healing. A variety of clinical studies show that LLLT in the near infrared range may be useful in the treatment of back pain.

Objective

To evaluate the efficacy of Light Therapy for treatment of back pain in pilots.

Study design: Prospective, randomized, controlled double blind. Volunteers will receive biweekly physiotherapy treatment for 3 weeks. In addition to the physiotherapy treatment, half the volunteers will receive light therapy and half sham irradiation. Study evaluations will include physical examination by an orthopedic surgeon, subjective pain level by visual analogue scale, validated low back functional questionnaires, a generic functional questionnaire, and patient satisfaction scores. Volunteers will be invited for evaluations at 1 and 3 months after the final treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Pilot (current)
  • Level of pain - moderate to severe low back pain (≥40 on the pain VAS)

排除标准

  • Low back pain due to non-traumatic etiological causes (infection, tumor, osteoporosis, ankylosing spondylitis, fracture, inflammatory process, cauda equinal syndrome).
  • Recent (up to 1 year) history of trauma
  • Current chronic pain other than low back pain
  • Physical disability that prevents the patient to lie down/get up

结局指标

主要结局

Time to reach minimal important change in pain level by visual analog scale (VAS)

时间窗: within 4 months

次要结局

  • Change in pain level by VAS after 3 weeks compared to baseline (before treatment)(3 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Lilach Gavish

Study Director

Hebrew University of Jerusalem

研究点 (1)

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