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Evaluating Different Low-level Laser Therapies to Treat Neck Pain in Air Force Pilots and Flight Crew

P

Paul Crawford

Status

Terminated

Conditions

Neck Pain

Treatments

Procedure: Group 1 -- using Pinnacle Series Laser Device
Procedure: Group 2 -- using Pinnacle Series Laser Device
Procedure: Group 3 -- using Phoenix Thera-Lase Device

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT03945240
FWH20190105H

Details and patient eligibility

About

Determine the most effective and efficient treatment protocols for treating neck pain with LLLT.

Full description

The purpose of this study is to identify what are the most effective low level laser therapy (LLLT) dosimetry parameters when treating pilots and navigators complaining of flight related neck pain.

Enrollment

80 patients

Sex

All

Ages

18 to 62 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

**Patients must be able to get care at Nellis Air Force Base (a military installation) in order to participate in this study**

Inclusion Criteria:

  • Active Duty US Air Force pilots or onboard navigators, aged 18- 62 years of age
  • maintain operational flight status at enrollment or within the last 6 months
  • History of neck pain for a period of more than two months
  • Score on the Neck Disability Index ranging from 15-24
  • No physiotherapy or local injection in 3 months before starting the study

Exclusion Criteria:

  • pregnant
  • major surgery or trauma in the previous 3 months
  • unstable cervical spine
  • cervical radiculopathy
  • rheumatoid arthritis
  • open wound over neck
  • pace-maker or defibrillator implantation
  • overt neuropathic pain or radiation pain
  • inability to express pain or quality of life.
  • history of neurological disorders
  • medical diagnosis of fibromyalgia; systemic disease

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

80 participants in 3 patient groups

Group 1 (Pinnacle, lower dosimetry parameters)
Experimental group
Description:
Utilize the Pinnacle Series Laser by Aspen Laser Systems to apply LLLT
Treatment:
Procedure: Group 1 -- using Pinnacle Series Laser Device
Group 2 (Pinnacle, higher dosimetry parameters)
Experimental group
Description:
Utilize the Pinnacle Series Laser by Aspen Laser Systems to apply LLLT
Treatment:
Procedure: Group 2 -- using Pinnacle Series Laser Device
Group 3 (Phoenix)
Experimental group
Description:
Utilizing the Phoenix Thera-Lase by Phoenix Thera-Lase Systems, we will apply LLT.
Treatment:
Procedure: Group 3 -- using Phoenix Thera-Lase Device

Trial contacts and locations

1

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Central trial contact

Jill M Clark, MBA

Data sourced from clinicaltrials.gov

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