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Chronic Pain Mind-Body Education Research: Volunteers Needed

• The purpose of this IRB approved research is to better understand the ways
in which a program of pain-related education and guided mind-body
exercises might affect patients’ experience with chronic pain
• All participation is voluntary
• Participants will not be paid

You might be eligible if:
• You are not currently participating in other kinds of pain or mind-body educational programs
• You have chronic pain and have ongoing supervision with a healthcare provider

Program information:
• This will be a live, interactive, online program that is conducted with each participant individually
• Participants will be asked to fill out several surveys and to attend the program for about 2 hours once a week for 5 weeks
• The program is free for eligible participants

Who is conducting the research:
• This research is being conducted by a graduate student (doctoral candidate) of the Depth Psychology/Somatic Studies program at Pacifica Graduate Institute (see Pacifica.edu)

Please note:
Participation in this research will not include medical or psychiatric assessment, diagnosis or management of your chronic pain or other physical or mental health issues. Participation in this research does not include evaluation of your current medical plan of care. You will continue to follow up with your health care providers for all your medical or mental health questions and needs. You should seek care from a medical or mental health professional as needed and for any new concerns.

For more information and to speak to the researcher, please contact:
Ph. 206.445.2493


Previous Research


Drug-Drug Interaction Between Orally Administered Hydrocodone-Acetaminophen and Inhalation of Cannabis Smoke: A Case Report

Ross Jason Bindler1 , Christy J. W. Watson1, Abram J. Lyons1, Lillian Skeiky1, Jamie Lewis2, Michael McDonell1, Philip Lazarus1, and Marian Wilson1


Objective: To determine if a 2-day protocol measuring pharmacokinetic and pharmacodynamic characteristics can demonstrate drug-drug interactions when smoked cannabis is added to orally administered hydrocodone/acetaminophen combination products. Case Summary: A 51-year-old non-Hispanic white male with chronic pain diagnoses participated in a 2-day pilot protocol. The participant attended two 7-hour in-lab days where he received 10 blood draws each day and completed self-administered pain and anxiety surveys. For both days, the participant took his prescribed dose of hydrocodone/acetaminophen (1/2 tablet of 7.5 mg/325 mg combination product) with the addition of 1 smoked pre-rolled marijuana cigarette (labeled as 0.5 g; 22.17% Δ9-tetrahydrocannabinol; 0.12% cannabidiol) on Day 2. Blood specimens were analyzed using mass spectrometry to quantify the difference of plasma hydrocodone levels between Day 1 and Day 2.

Results: Compared to Day 1, lower levels of pain and anxiety were reported during Day 2 with the addition of cannabis to oral hydrocodone/acetaminophen. Day 2 pharmacokinetic analysis also revealed more rapid absorption and overall lower levels of hydrocodone in plasma. Discussion: Lower hydrocodone plasma levels in Day 2 may indicate cannabis’s effect on metabolism and reduce the risk of opioid toxicity. The quicker absorption rate of hydrocodone could explain lower pain and anxiety scores reported on the second day. Conclusion and Relevance: A 2-day protocol was able to capture differences across time in pharmacokinetic and pharmacodynamic measurements. Larger studies can be designed to better characterize the potential drug-drug interaction of cannabis and opioids.

Learn more.

Program Evaluation of a Home Exercise Program for Chronic Back Pain in the Outpatient Setting

Xiang Jing, DNP and Jamie Lewis, MD


Research indicates many different interventions are potentially therapeutic in managing chronic back pain. While home exercise programs may be cost-effective for individuals, little has been published on the subject of how best to combine functional and psychologic instruments to measure structured exercise programs in an outpatient setting. This DNP project conducted a program evaluation of a pilot project which reviewed the efficacy of a home exercise program for people with chronic back pain. The project was approved by a multi-disciplinary team at a private spine and pain specialty practice. Participants were recruited from patients at this practice, 14 of whom completed this three-month pilot project with no reported adverse events. The program measured participants’ exercise pattern changes, back functional improvement, and compliance to the change of routine through the use of three validated questionnaires: Fear-Avoidance Beliefs Questionnaires (FABQ), Low Back Pain Disability Questionnaire (OSWESTRY), Exercise Self Efficacy Scale (ESES). The program evaluation provided valuable information on how a HEP may further adapt these measurement tools to provide relevant data in a fast-paced outpatient pain management setting.

Citation: Jamie Lewis, MD,  Karlee De Monnin, BS,  Jonathan Smith, BS,  Evan Lewis, Marian Wilson, PhD, MPH, RN (12 March 2021). Pain Medicine, pnab082, https://doi.org/10.1093/pm/pnab082

Goalistics Chronic Pain Program

Northwest Spine and Pain Medicine partnered with Washington State University on a research program looking at efficacy of Goalistics Online Pain Program combined with health coaching at treating chronic pain. Validating the effectiveness of Goalistics Chronic Pain Program and other online modalities helps to increase the scope of treatment options readily available to those suffering from chronic pain.

Building Efficacy for Successful Opioid Tapering

It can be challenging to decrease or discontinue opioid pain medication. Northwest Spine and Pain Medicine partnered with Goalistics, LLC to evaluate a new tool to help patients who are undergoing medically supervised opioid tapering. The development and testing of the Building Efficacy for Successful Tapering (BEST) Program is funded by a grant from the National Institute on Drug Abuse. The online BEST Program was designed to:

  • Teach pain patients about different methods of pain management that don’t involve pain medication
  • Help them to build their own custom list of “pain reducers”
  • Allow them to track and test the effectiveness of each method
  • Identify the best strategies for them

Two studies were conducted. The first study is a review of the BEST program by patients who are currently undergoing opioid tapering. Their feedback will help ensure that the BEST Program is user-friendly and beneficial to future program users. The second study is a pilot randomized controlled trial to examine the efficacy of the program.

T. Bigand, M. Wilson, S. Riedy, J. Lewis (2017). Cannabis use is related to self-efficacy but not sleep or pain symptoms: A survey of adults prescribed opioids for pain or opioid use disorders [abstract]. The Journal of Pain. 12.121

Inadequate pain management and sleep difficulties are commonly reported by people using opioids to treat persistent pain or for medication-assisted treatment of Opioid Use Disorder (OUD). Cannabis use is frequently reported within both populations to manage pain and sleep problems, although how cannabis influences co-occurring symptoms is uncertain. Self-efficacy, the confidence that one can control symptoms, can improve pain and sleep symptoms. It remains unknown how cannabis use relates to self-efficacy in managing symptoms of pain and sleep. To explore relationships between cannabis use, sleep quality, pain intensity, and self-efficacy, survey data of adults prescribed opioids for OUD (n = 150) and persistent pain (n = 150) were analyzed. The Pittsburgh Sleep Quality Index (PSQI) global score and Patient-Reported Outcomes Measurement Information System (PROMIS) pain intensity and self-efficacy subscale scores were used to assess sleep quality, pain intensity, and self-efficacy, respectively and a questionnaire assessed cannabis use. Data were analyzed using linear regression with main effects for sample (OUD and persistent pain) and cannabis use (yes/no) in the last month and their interaction. Overall, 87% of all surveyed adults had clinically relevant poor sleep quality (PSQI > 5). Better sleep quality was associated with greater self-efficacy (F1,225 = 23.30, P < .001) and less pain intensity (F1,230 = 29.95, P < .001). Cannabis use in the last month did not predict sleep quality or pain intensity (P > .70). Cannabis users had higher self-efficacy scores than non-users (F1,277 = 6.78, P = .01). Persistent pain patients had poorer sleep quality (F1,225 = 10.14, P = .001) and greater pain intensity (F1,281 = 32.43, P < .001) than OUD patients; self-efficacy did not differ (F1,277 = .27, P = .60). Evidence does not support cannabis for improving pain or sleep for either group, yet cannabis users have more confidence in symptom control. Future studies should focus on interventions that reduce symptom burden while enhancing self-efficacy.

Citation: Marian WilsonMyles FinlayMichael Orr Celestina Barbosa-LeikerNaghmana SheraziMary Lee A RobertsMatthew LaytonJohn M Roll (2018). Engagement in online pain self-management improves pain in adults on medication-assisted behavioral treatment for opioid use disorders [abstract]. PubMed.gov Nov;86:130-137

Citation: Bigand, T., Roberts. M., Lewis, J., Wilson, M. (2019). Coaching to increase engagement in online pain self-management program [abstract]. Pain Management Nursing, 20(2),96.