Clinical Trial Finder

Inclusion Criteria:

• - Confirmed clinical diagnosis of neuropathic pain AND.

• - Confirmed clinical diagnosis of Post-treatment Lyme disease syndrome.

• - Diagnosis will be based on participants meeting either Group 1 or Group 2 criteria of the Columbia Clinical Trial Network PTLDS diagnostic criteria: - Group 1.

Well-defined Lyme disease meeting CDC Surveillance Definition.

• - Erythema Migrans.

• - History of possible exposure to a high incidence county or state (or an adjacent area) - Erythema migrans rash.

• - EM 1: EM rash diagnosed by HCP previously (either in person or telemedicine) - EM 1A: MOA self-report & medical record documentation of rash > 5 cm.

• - EM 1B: MOA: self-report and medical record documentation of EM rash but not size.

• - EM 1C: MOA: self-report & rash misdiagnosed in medical record as cellulitis/spider bite.

• - EM 1D: MOA: self-report and either: photo of EM or Class 1 lab test confirmation within 4 weeks of illness onset OR Disseminated "objective" manifestation with lab test confirmation of Bb infection.

• - Clinical history includes at least one of the following symptoms/signs, which are not better accounted for by another cause (MOA: medical records and/or self-report).

• - Neurologic: Lymphocytic Meningitis; Encephalitis; Encephalomyelitis, Cranial Neuritis (especially facial palsy); Radiculoneuropathy; - Other Neurologic Signs (with objective measures): Encephalopathy, Polyneuropathy.

• - Carditis: 2nd or 3rd degree AV block; Myocarditis; Pericarditis.

• - Lyme arthritis: Recurrent joint swelling in one or more joints.

• - Dermatologic: Disseminated EM ("satellite") or Acrodermatitis atrophicans AND.

• - Lab test Confirmation (previous) (requires at least one of the Class 1 lab tests) (MOA: self-report & documentation) Group 2.

Probable.

• - Chronic Multisystem Symptoms attributed to Lyme disease (insufficient to meet Group 1) and not better explained by another diagnosis and patient has evidence of positive lab results on a Class 1 lab test (or 4 of 10 bands for IgG Western blot (WB)) (MOA: self-report with lab documentation.

• - Class 1 lab test confirmation (excluding IgM WB) - Highly suggestive IgG WB (4 of 10 bands) OR EM rash by history after exposure to a Lyme-endemic area but not previously diagnosed by a HCP and no photo or Class 1 lab test confirmation is available (MOA: self-report) OR Viral like illness (not better explained by other cause) with indeterminate or + enzyme immunoassay (EIA) with positive IgM WB or positive Class 1 lab test (within 4 weeks of illness onset after known exposure to a Lyme high-incidence area for standard two-tiered (STT) IgM) (MOA: medical records, lab test and self-report) (MOA: lab test and self-report) OR.

• - Viral like illness (not better explained by other cause) with indeterminate or positive EIA with positive IgM WB or positive Class 1 lab test (within 6 months of illness onset after known exposure to a Lyme high-incidence area for standard twotiered (STT) IgM) (MOA: medical records, lab test and self-report) (MOA: lab test and self-report) - Ages 18+ - Fluent in English.

• - Consistent medications for the last 4 weeks prior to the first baseline visit (week 0)

  Exclusion Criteria:

  - Diagnosis of photosensitive epilepsy.

• - Ear or eye infection.

• - Vision impairments that affect perception of light in one or both eyes.

• - Deafness in one or both ears.

- Psychiatric disorders (participants will not be excluded if they score 0-30 points on the BDI, or if participants self- report having anxiety)

Arms

Experimental: Real Arm

This group will experience the active device settings.

Sham Comparator: Sham Arm

This group will experience the sham device settings.

Interventions

Device: - Sana Pain Reliever

The Sana Pain Reliever (Sana PR) by Sana Health Inc is a device comprised of one (1) main component (Mask with Earbuds) and two (2) ancillary components (Charger and Headband). The device is worn over the eyes (with earbuds in ears).

Device: - Sham SPR

Participants will receive the SPR device and a tablet with instructions of how to use the device and how to answer the questionnaires on the tablet mobile application. Each session with the device will last 15 minutes and run under the device's sham settings. The session consists of periods of light and sounds (beeps). Participants will be instructed to use the device each day at the end of the day prior to going to sleep and whenever they experience heightened pain during the day.