Pragmatic Comparative Effectiveness Trial of Evidence-based, On-demand, Digital Behavioral Treatments for Chronic Pain

Chronic Pain Clinical Trial

Official title:

Transcending COVID-19 Barriers to Pain Care in Rural America: Pragmatic Comparative Effectiveness Trial of Evidence-based, On-demand, Digital Behavioral Treatments for Chronic Pain

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04933474
• Other study ID #: STUDY00001262
• Secondary ID: 1R01NR019947-01
• Status: Active, not recruiting
• Phase: N/A
• Start date: March 23, 2022
• Est. completion date: June 30, 2024

Study information

• Verified date: March 2024
• Source: Cedars-Sinai Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will compare two available, evidence-based, digital pain treatment programs that patients can use at home. The goal is to see if one approach is better than the other, and whether certain patients respond to one more than the other. Study participants will be randomized to receive one of two treatment programs: Skills-Based VR or painTRAINER. Study devices will be delivered to the participant's home with instructions for use via FedEx; participants will receive remote technical support. They will be followed for 60 days and complete Patient Reported Outcome (PRO) questionnaires to assess functional status, pain levels, and use of pain medications (including opioids). Participants will also be asked to provide consent/authorization to access medical records from their treating facility.

Description:

We will perform a two-arm, multi-center, vRCT in a geographically diverse group of patients with mixed-etiology chronic pain. Using a random number generator, patients will be allocated in a 1:1 ratio between two self-administered, remotely deployed CBT delivery platforms, stratified by site: (1) a 2D mHealth app called PainTRAINER; and (2) 3D VR app called EaseVRx. The primary analysis will compare changes in pain intensity over two months upon completion of the standardized 8-week digital CBT protocols. Secondary outcomes will include pain catastrophizing, Coronavirus-related anxiety, pain interference, self-efficacy, and opioid use. Although complete patient blinding can be challenging in digital health studies, particularly those using VR, we will follow the VR-CORE guidance and previous VR trial precedent by informing patients that researchers are testing the effect of "two types of audiovisual experiences on the perception of pain". Because it is important for researchers to exhibit equipoise when describing the competing interventions, we will prepare a script that uses neutral language regarding the two interventions, as per previous VR research. In addition, data analysts will be blinded to patient allocation.

We will employ broad inclusion criteria to maximize the external validity of the study and generalizability of results. In consulting with our patient partners who co-developed this application, we opted to study pain and distress for individuals with all forms of chronic pain except active cancer treatment and end-of-life care. The population impacted by this research thus broadly encompasses individuals with many different types of chronic pain conditions, including somatic, musculoskeletal, neuropathic, and visceral pain. More than 60% of individuals with chronic pain are women, and although the point prevalence for chronic pain increases with age, 35% of individuals 45-54 years of age report some form of chronic pain condition, and often multiple pain conditions. In terms of race and ethnicity, 81-85% report their race and ethnicity as non-Hispanic White, 8-9% identify as non-Hispanic Black, and 5-9% as Hispanic.

This vRCT will be conducted remotely using a process our team has developed and applied in many previous virtual trials, including in a current NIH-sponsored trial for chronic lower back pain. Patients will be recruited using pre-existing large registries within our consortium and will complete consent forms, receive study materials, and speak with study staff all from their home without requiring in-person visits. Patients will be recruited from three major sites: (1) Cedars-Sinai Health System (CSHS); (2) Ochsner Health; (3) UAB. At all sites, participants identified by search tools will be contacted by a combination of mail, email, and patient-portal notifications and offered an opportunity to opt-in or opt-out; those who do not respond will receive a follow-up phone call.

We will compare two digital platforms, both currently in wide use and supported by evidence, that deliver self-administered, 8-week, home-based CBT-based treatment programs for patients with chronic pain and distress: PainTRAINER (2D mHealth intervention) and EaseVRx (3D VR intervention).

We will employ a biopsychosocial conceptual framework for monitoring outcomes in the trial, focusing on pain intensity as the primary outcome, and including a range of other relevant PROs selected in partnership with our patient partners. PROs will be collected via REDCap. Pain intensity will be measured using a standard 11-point numeric rating scale (NRS) with a 24-hour recall. Consistent with NIH Helping to End Addiction Long-Term (HEAL) guidance, we will measure daily pain NRS for 7-days during baseline week 0, and again during the final week of the study (week 8). The minimally clinically importance difference (MCID) on the pain NRS is 2 points. Secondary Outcomes: Secondary outcomes will include the 4-item short form pain catastrophizing scale, 5-item Coronavirus Anxiety Scale, 8-item NIH PROMIS Pain Interference scale, 2-item Pain Self-Efficacy Questionnaire, and opioid usage in morphine milligram equivalents (MMEs). In addition, we will measure satisfaction with assigned treatment using the Pain Treatment Satisfaction Scale and will monitor for VR cybersickness using the Simulator Sickness Questionnaire (SSQ).

To learn more about the study and to assess your eligibility, please visit our study website at https://virtualmedicine.org/research/current/tech4pain

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 300
• Est. completion date: June 30, 2024
• Est. primary completion date: March 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 13 Years to 99 Years

Eligibility

We will recruit patients who: (1) have chronic pain, from any underlying condition, using the administrative definition of ICD-10 code series G89.X or one or more of 134 chronic overlapping pain condition codes, as previously standardized and validated by an expert panel; (2) have experienced average pain intensity of >3 out of 10 within the previous week; (3) are =13 years of age; (4) are able to read/write English; (5) have either a personal computer or a smartphone; and (6) live in a designated rural zip code as defined by the Federal Office of Rural Health Policy (FORHP) data.

We will exclude patients who: (1) have a condition that interferes with use of the intervention (e.g., visual impairment); (2) are hospitalized; (3) are receiving active cancer treatment; (4) are receiving end-of-life care; or (5) have cognitive impairment that affects participation. We will stratify analyses across key patient characteristics, including type of pain condition, sex, age, race, ethnicity, State and zip code, Rural-Urban Commuting Area (RUCA) codes (a composite measure of population density, urbanization, and daily commuting), pain severity, opioid use, comorbidities, social support, and COVID-19 impacts (unemployment, financial hardship, family or personal COVID-19 diagnosis).

Related Conditions & MeSH terms

• Chronic Pain

Intervention

Behavioral:
• painTRAINER®
PainTRAINER is among the most widely-validated mHealth interventions for pain management.18-25 Originally developed by members of our team at Duke and Northwestern University under NIH funding, the app teaches evidence-based pain coping skills using a self-administered, home-based software program. The system delivers eight sessions via any web-connected platform, including Android or iOS smartphones, tablets, or personal computers. The digital curriculum covers progressive muscle relaxation, activity/rest cycling, pleasant activity scheduling, recognizing negative automatic thoughts, pleasant imagery/distraction, problem solving, and monitoring for maintenance. Patients complete one session per week in a pre-determined order. The program can be completed in a flexible manner to accommodate life and medical events.

Device:
• PICO G2 4k
Patients allocated this arm will use a multi-modal, skills-based, selfmanagement VR program, called EaseVRx. Developed by AppliedVR (Los Angeles, CA) in partnership with Stanford pain psychologist Dr. Beth Darnall, the program teaches and trains users based on evidenced-based strategies and biofeedback exercises. EaseVRx combines psychoeducation, pain education, breathing training, relaxation exercises, and executive functioning games to provide a mind-body approach toward living better with pain. The standardized, reproducible, 56-day program delivers a combination of skills training and CBT-related treatments through scheduled daily virtual experiences. Each VR experience lasts between 2-16 minutes.

Locations

Country	Name	City	State
United States	Cedars-Sinai Medical Center	Los Angeles	California

Sponsors (6)

Lead Sponsor	Collaborator
Cedars-Sinai Medical Center	National Institute of Nursing Research (NINR), Northwestern University, Ochsner Health System, Stanford University, University of Alabama at Birmingham

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Daily Pain Intensity	Pain intensity will be measured using a standard 11-point numeric rating scale (NRS) with a 24-hour recall. Consistent with NIH Helping to End Addiction Long-Term (HEAL) guidance, we will measure daily pain NRS for 7-days during baseline week 0, and again during the final week of the study (week 8). The minimally clinically importance difference (MCID) on the pain NRS is 2 points.	Over 8 weeks from baseline
Secondary	PROMIS Pain Interference 4a	The pain interference scale measures the consequences of pain on relevant aspects of one's life. This includes the extent to which pain hinders engagement with social, cognitive, emotional, physical, and recreational activities. The scale is rendered using a T-statistic, where a score of 50 represents the population mean, and 10 points is a standard deviation (SD).	Over 8 weeks from baseline
Secondary	Pain Catastrophizing scale 4 item short form	Pain catastrophizing is a cascade of negative cognitions and emotions regarding actual or anticipated pain, and includes aspects of rumination, magnification, and sense of helplessness. Pain catastrophizing is a highly potent prognostic indicator for acute analgesic use, and acute and chronic pain outcomes, yet is also highly modifiable with behavioral treatment that enhances pain self-regulation via evidence-based skills. We will use the 4-item short form pain catastrophizing scale.	Over 8 weeks from baseline
Secondary	Pain Self-Efficacy Questionnaire (PSEQ) 2-item short form	Self-efficacy refers to confidence in one's ability to perform specific health-related tasks or behaviors. We hypothesize that the skill-based VR educational modules will improve self-efficacy. We will measure this domain using the Pain Self-Efficacy Questionnaire (PSEQ-2), a two-item instrument designed to assess the extent to which people in pain believe they are presently able to work and live a normal life despite pain (work includes housework and paid and unpaid work). There is strong evidence for the validity and reliability of the PSEQ-2, its sensitivity to change, and suitability in clinical and research settings.	Over 8 weeks from baseline
Secondary	Opioid prescriptions of Morphine Milligram Equivalents (MME)	Comparing the change from study baseline to Day 60 in weekly MME of prescribed medication.	Over 8 weeks from baseline
Secondary	Pain Treatment Satisfaction	Measures patient satisfaction for patients receiving treatment for chronic pain.	Week 8
Secondary	Treatment Expectation	Measures participant's expectation that participation in the study will help with their pain. Asked before and after the participant is randomized to measure a change in expectation once the participant is aware of the intervention allocation.	Baseline
Secondary	Coping with Weekly Pain Questionnaire	Measures whether or not individuals use a combination of behavioral and emotional coping strategies to cope with their pain. This instrument will serve as an assessment towards the development of skills over each 8-week program as well as whether these skills were used 30-days following completion of the program. Adapted from a daily instrument for arthritis pain to a 7-day average of general pain.	Over 12 weeks from baseline
Secondary	Treatment Usage Questionnaire	Measures level of engagement with study program, modified at week 12 to measure whether skills gained during program are still utilized 4 weeks following program completion.	Over 12 weeks from week 1

External Links

•   Study web portal for more information and a self-assessment for eligibility