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Light Therapy for the Treatment of Back Pain in Pilots (LLL&Pilots)

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

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02665507
Acronym
LLL&Pilots
Enrollment
42
Registered
2016-01-27
Start date
2018-03-01
Completion date
2024-07-03
Last updated
2025-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Back Pain

Keywords

Photobiomodulation, Aviation

Brief summary

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.

Detailed description

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.

Interventions

DEVICEGaAlAs 808nm laser

Hand held superpulsed GaAlAs 808 nm LLLI

DEVICESham

Hand held laser that emits no LLLI

Sponsors

Hebrew University of Jerusalem
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* Low back pain due to non-traumatic etiological causes (infection, tumor, osteoporosis, ankylosing spondylitis, fracture, inflammatory process, cauda equinal syndrome). * Pregnant * 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

Design outcomes

Primary

MeasureTime frame
Time to reach minimal important change in pain level by visual analog scale (VAS)within 4 months

Secondary

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

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026