Prospective Assessment of Integrative Therapies for Neuromusculoskeletal Pain (PAIN)

All of the below items are research-related unless marked as 'standard of care'. Visits will vary depending on provider-decided treatments and will generally range from 30 minutes to 2 hours in length.

Self-reported pain intensity assessment.

Screening visit (1 hour):

• Obtain and document signed Informed Consent document and HIPAA Authorization
• Verify subject eligibility based on inclusion/exclusion criteria. Medical record will verify inclusion.
• -Record all medications including over the counter the subject is taking. Record morphine milligram equivalents (MME) for patients taking opioid medications. Collect basic demographic information to include phone number, email address, DoD ID, age, race, ethnicity, assigned sex at birth, weight (pounds), height (inches), and BMI, estimated annual income.
• Collect additional information to include:

• Beneficiary Status (Active-Duty, Retired Active-Duty, dependent, Reservist)
• rank (if applicable),
• employment status and description (full time, part time, unemployed, retired, homemaker) number of deployments (if applicable), Marital status (Married, Domestic Partners, Divorced, Widow/er, separated, single/never married)
• education (military training; high school/GED; some college; 2 year college; 4 year college; some graduate work; completed master's or professional degree; completed Ph.D., law degree, MD, similar advanced professional degree)
• Patient History, was there a precipitating injury, location of pain (neck, thoracic, or lumbar), history of surgery and type of surgery, any history of pain management interventions (injections, ablations, etc) especially related to the subject's chronic axial spine pain
• Other therapies for their condition currently receiving or in the last 3 months (ie chiropractic, physical therapy, pain management etc) Randomization: Subjects will not be randomized as this is a single armed cohort study. Subjects will be assigned a unique study code in sequential order beginning with 001.

SURVEY RELATED VISITS

Visit 1 (week 0 can be the same day as screening visit) (30 minutes) (In-person or Virtual):

BASELINE

• Subject will fill out the following Standard of Care Patient Questionnaires:
• PROMIS Physical Function Form 6b
• 6 questions evaluating physical function
• DVPRS 0-10 Scale
• pain assessment tool using numerical rating scale enhances by functional word descriptors, color coding, and pictorial facial expressions
• PEG
• Assesses pain intensity and interference
• Patient Health Questionnaire 2-item (PHQ-2)
• Measures depressed mood and anhedonia over past 2 weeks
• Survey is extended to a 9-item PHQ-9 only for subjects scoring 3 or higher on the PHQ-2
• Generalized Anxiety Disorder 2-item (GAD-2)
• Screening tool for generalized anxiety disorder
• Survey is extended to a 7-item GAD-7 only for subjects scoring 3 or higher on the GAD-2
• Pain Catastrophizing Scale
• Quantifies pain experience (rumination, magnification, and helplessness)
• Pittsburgh Sleep Quality Index
• Dallas Pain Questionnaire
• 16 item quality of life questionnaire assessing multiple domains
• Patient receives treatment preferably same day, but within 72 hours
• Scores may be pulled from patient Electronic Medical Record

Visit 2 (Week 4) (60 minutes) (In-person or Virtual) Research coordinator with record morphine milligram equivalents (MME) for patients taking opioid medications.

• Subject will complete the following Standard of Care Patient Questionnaires:
• PEG
• PHQ-2 or PHQ-9 (PHQ-2 score > 2)
• GAD-2 or GAD-7 (GAD-2 score > 2)
• Pain Catastrophizing Scale
• Pittsburgh Sleep Quality Index
• DVPRS 0-10 Scale
• PROMIS Physical Function Form 6b
• Dallas Pain Questionnaire
• Scores may be pulled from patient Electronic Medical Record

Visit 3 (Week 8) (60 Minutes) (In-person or Virtual) Research coordinator with record morphine milligram equivalents (MME) for patients taking opioid medications.

• Subject will complete the following Standard of Care Patient Questionnaires:
• PEG
• PHQ-2 or PHQ-9 (PHQ-2 score > 2)
• GAD-2 or GAD-7 (GAD-2 score > 2)
• Pain Catastrophizing Scale
• Pittsburgh Sleep Quality Index
• DVPRS 0-10 Scale
• PROMIS Physical Function Form 6b
• Dallas Pain Questionnaire
• Scores may be pulled from patient Electronic Medical Record

Visit 4 (Week 12) (60 Minutes) (In-person or Virtual) Research coordinator with record morphine milligram equivalents (MME) for patients taking opioid medications.

• Subject will complete the following Standard of Care Patient Questionnaires:
• PEG
• PHQ-2 or PHQ-9 (PHQ-2 score > 2)
• GAD-2 or GAD-7 (GAD-2 score > 2)
• Pain Catastrophizing Scale
• Pittsburgh Sleep Quality Index
• DVPRS 0-10 Scale
• PROMIS Physical Function Form 6b
• Dallas Pain Questionnaire
• Patient receives treatment at provider discretion
• Scores may be pulled from patient Electronic Medical Record

Visit 5 (Week 16) (60 minutes) (In-person or Virtual) Research coordinator with record morphine milligram equivalents (MME) for patients taking opioid medications.

• Subject will complete the following Standard of Care Patient Questionnaires:
• PEG
• PHQ-2 or PHQ-9 (PHQ-2 score > 2)
• GAD-2 or GAD-7 (GAD-2 score > 2)
• Pain Catastrophizing Scale
• Pittsburgh Sleep Quality Index
• DVPRS 0-10 Scale
• PROMIS Physical Function Form 6b
• Dallas Pain Questionnaire
• Scores may be pulled from patient Electronic Medical Record

Visit 6 (Week 20) (60 minutes) (In-person or Virtual) Research coordinator with record morphine milligram equivalents (MME) for patients taking opioid medications.

• Subject will complete the following Standard of Care Patient Questionnaires:
• PEG
• PHQ-2 or PHQ-9 (PHQ-2 score > 2)
• GAD-2 or GAD-7 (GAD-2 score > 2)
• Pain Catastrophizing Scale
• Pittsburgh Sleep Quality Index
• DVPRS 0-10 Scale
• PROMIS Physical Function Form 6b
• Dallas Pain Questionnaire
• Scores may be pulled from patient Electronic Medical Record

Visit 7 (Week 24) (60 minutes) (In-person or Virtual) Research coordinator with record morphine milligram equivalents (MME) for patients taking opioid medications.

• Subject will complete the following Standard of Care Patient Questionnaires:
• PEG
• PHQ-2 or PHQ-9 (PHQ-2 score > 2)
• GAD-2 or GAD-7 (GAD-2 score > 2)
• Pain Catastrophizing Scale
• Pittsburgh Sleep Quality Index
• DVPRS 0-10 Scale
• PROMIS Physical Function Form 6b
• Dallas Pain Questionnaire
• Scores may be pulled from patient Electronic Medical Record

Visit 8 (Week 28) (60 minutes) (In-person or Virtual) Research coordinator with record morphine milligram equivalents (MME) for patients taking opioid medications.

• Subject will complete the following Standard of Care Patient Questionnaires:
• PEG
• PHQ-2 or PHQ-9 (PHQ-2 score > 2)
• GAD-2 or GAD-7 (GAD-2 score > 2)
• Pain Catastrophizing Scale
• Pittsburgh Sleep Quality Index
• DVPRS 0-10 Scale
• PROMIS Physical Function Form 6b
• Dallas Pain Questionnaire
• Scores may be pulled from patient Electronic Medical Record
• Treatment Helpfulness Questionnaire
• Active duty members will be asked if duty, fitness or mobility restrictions were lifted during the study period

TREATMENT VISITS Treatments given in Integrative Medicine Clinic will be at provider discretion. Subjects will attend a minimum of 3 visits then additional treatment sessions will be at provider discretion as well.

The following semi structured clinical algorithm will be used by providers in the clinic.

Visit 1:

• Initial interview with focus on whole person
• Microcurrent standard protocols (Standard concussion protocol, Spinal Cord long)
• Myofascial work to include transverse abdominus teaching, rectus abdominus release, other myofascial, time permitting or as needed
• Optional Loan of microcurrent box with protocols at physician discretion
• Optional loan of avazzia or alpha stim at physician discretion
• Home Exercise Program handout (HEP2go)

Visit 2:

• Assess effect of prior myofascial work
• Re-education of TA activation, additional myofascial work as needed (including lower trap and

/or glut med activation)

• Assess effect of Microcurrent
• Optional Loan of microcurrent box with protocols at physician discretion
• Optional loan of avazzia or alpha stim at physician discretion
• create plan for visit 3 (this could include additional myofascial work, shock wave therapy, acupuncture/dry needling, avazzia or alpha stim)

Visits 3 through final:

• Continue treatment with any or all of the following modalities

a. Myofascial treatments (functional neuromyofascial techniques [FNT], cupping, gua sha, active needling) b. Frequency Specific Microcurrent (FSM) c. Avazzia d. Extracorporeal shock wave therapy (ESWT) e. Acupuncture/dry needling f. Alpha stim (cranio-electric stimulation) Coordinators will monitor subject visits either in-person post each visit or by accessing the EMR post each visit to record visit details. Visit Details to Record

• Visit Number (1-10, >10)
• ICD-10 codes
• Examples
• M54.2 Cervicalgia
• M54.5 Low Back Pain
• M79.7 Fibromyalgia
• Z73.3 PTSD*
• M54.9 Dorsalgia, unspecified
• F41.9 Anxiety
• M25.51 Shoulder Pain
• M54.6 Thoracic Spinal Pain
• M72.2 Plantar Fasciitis
• L90.5 Scar Conditions and Fibrosis of Skin
• Modalities Used
• Examples
• Myofascial modalities (FNT, cupping, scraping/gua sha, active needling)
• FSM
• Avazzia
• Acupuncture
• Dry needling
• Alpha Stim
• ESWT

**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 and DoD Beneficiaries (i.e. former military, spouse, dependent child) aged 18 or older referred to the Nellis Integrative Medicine Clinic chronic back or neck pain
• Pain Chronicity Threshold (pain score ≥4/10 documented in EMR or reported by patient at least 2 times in one year and at least 30 days apart).

Exclusion criteria

• Enrolled in other pain management program (e.g. pain management, PT

/OT)

• Anticipated Change of station, deployment, retirement from military service, separation from active or reserve military service (includes national guard) or plan to discontinue enrollment at MOMMC in <6 months
• Planned surgery during the study period
• Pregnancy
• <3 months post-partum
• Hypermobility disorders such as Ehlers Danlos
• Active cancer (cancer in remission is not an exclusion)
• Implanted electrical devices that cannot be turned off (ie pacemaker); implanted stimulators or pumps that can be turned off are not exclusionary
• Injury or surgery within the last 6 weeks
• Dementia
• Delirium
• Inability to make medical decisions or understand treatment plan as decided upon by principle or associate investigators
• Undergoing medical evaluation board
• Currently in the process of establishing or appealing VA disability rating, or planning to do so within the study period