Research context

The NASA 2020 feasibility assessment

A 2020 NASA feasibility report reviewed over 1,600 records on drug-free pain relief for long space missions and ranked ActiPatch® first.

This ranking is about spaceflight practicality only. It is not a NASA endorsement, not clinical evidence and not a finding that any one approach relieves pain better than another. ActiPatch® is FDA-cleared for adjunctive treatment of musculoskeletal pain, and this report does not change that.

Did NASA rank ActiPatch® first for pain relief in space?

No. A 2020 report prepared at NASA’s Johnson Space Center ranked 4 drug-free device approaches by how easy they would be to use in spaceflight, and pulsed shortwave therapy, the technology in ActiPatch®, ranked first. The report did not compare how well the approaches relieve pain, and it is not a NASA endorsement.

The ranking

Order of perceived ease of implementation in spaceflight, from Table 5-1 of the report.

RankApproachHow it is appliedPractical notes in the report
1Pulsed shortwave therapy (PSWT)A small wearable loop placed over the painful areaExample listed: ActiPatch® (BioElectronics Corp). Over the counter, no treatment sensation, 720-hour disposable battery.
2UltrasoundWearable pads that deliver sound waves into tissuePrescription home use, 6-hour rechargeable battery.
3PhotobiomodulationHandheld laser or LED light applied to the skinOver the counter, 8-hour rechargeable battery, 5-minute sessions.
4TENSElectrical current through electrodes on the skinOver the counter. Stimulation is set just below the pain threshold, which some users dislike.

The report also noted limits for PSWT: finite battery life and effects that are not selective about which nerve signals they change. Its recommendations were to obtain an ActiPatch® device for further evaluation and to connect with pain research at the Department of Defense and the National Institutes of Health.

What it assessed

  • Published research, patents and federal grant databases, searched digitally between July and September 2020. More than 1,600 database records were screened and 77 were used in the final summary.
  • Which existing pain treatments might suit long missions, where medicines have limited shelf life and resupply is hard.
  • Non-invasive devices that act on the nerves outside the brain and spinal cord, ranked by how practical they would be to use in spaceflight.

What it did not assess

  • No device was tested on people, in a laboratory or in space as part of this report.
  • It did not compare how well the four approaches relieve pain.
  • Medicines, exercise, mind and body methods, implanted or needle-based procedures and brain stimulation were outside its focus.
  • The author notes the search was not exhaustive because libraries were closed during the COVID-19 pandemic.

About the source

Carol Mullenax, “Electromagnetic Pain Relief/Blocking: Feasibility Assessment,” NASA Johnson Space Center, 24 September 2020. A contractor technical report funded by the center’s 2020 Innovation Charge Account program and published on the NASA Technical Reports Server (NTRS).