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Can Medical Cannabis Affect Opioid Use?

Recruiting
Conditions
Pain
Chronic Pain
Interventions
Other: Medical Cannabis
Registration Number
NCT06206252
Lead Sponsor
Thomas Jefferson University
Brief Summary

The goal of this observational study is to learn how medical cannabis (MC) affects pain and the use of opioid pain medications. Participants who have chronic pain and use prescribed opioid pain medication will opt-in to using MC or not for the 3-month study. Participants who are certified in Pennsylvania will purchase specific medical cannabis products at a reduced cost from a partnering medical cannabis dispensary monthly. All participants will complete baseline, daily, and monthly assessments to observe changes across groups.

Detailed Description

The primary aim is to observe if individuals who have chronic pain that they are treating with opioids and medical cannabis report changes in pain severity, function, and opioid use compared to those who do not use medical cannabis.

Secondary aims include observation of whether the use of medical cannabis differentially impacts tolerability (side effects, risk of cannabis use disorder), sleep-related symptoms, or quality of life and mental health among chronic opioid users.

There will be two groups, participants who are certified to use medical cannabis and those who do not use any cannabis. All participants will complete a baseline survey to report demographics, pain, sleep, mental health, well-being, quality of life, and use of medications. Some of these questions will be repeated monthly. Participants will also receive a link via text to a daily survey to report daily prescription opioid use and medical cannabis use (if applicable) as well as pain severity and interference.

Participants who purchase medical cannabis at Ethos will be randomized and restricted to one formulation of medical cannabis (vaporization or tincture) for the study duration. They will purchase three different compositions of the specific medical cannabis formulation at a reduced cost over 3 months and the order of those compositions will be randomized. They will purchase one composition per month and they will not know which one they are purchasing. The three different compositions are:

* A composition that is predominantly THC (tetrahydrocannabinol)

* A composition that is predominantly CBD (Cannabidiol)

* A composition that is a one-to-one blend of THC and CBD

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
110
Inclusion Criteria
  • Current diagnosis of chronic, intractable pain
  • Use of prescription opioids for longer than 90 days
  • Have a smartphone or agree to use one provided
  • English fluency
  • Medical cannabis group only: Willing to get certified by a physician to use medical cannabis in PA OR already certified but have not been using medical cannabis products regularly (daily or weekly) for longer than 30 days
  • Medical cannabis group only: Willing to accept a temporary restriction on medical cannabis products
  • Control group: Agree to continue not using cannabis for the duration of the study (3 months)
Exclusion Criteria
  • Under 18 years old
  • Being under conservatorship
  • Self-reported pregnant or breastfeeding
  • Cannabis Use Disorder
  • Active treatment in methadone or buprenorphine program for Opioid Use Disorder
  • Diabetic neuropathy or chemotherapy-induced neuropathy alone
  • Medical cannabis group: Cannabis use (daily/weekly) for more than 30 days
  • Control group: Cannabis Use

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Medical Cannabis GroupMedical CannabisParticipants will use designated medical cannabis products for the study duration.
Primary Outcome Measures
NameTimeMethod
Change in pain interferenceBaseline, 4 weeks, 8 weeks, 12 weeks

Assessed using Brief Pain Inventory Short Form (BPI-SF), scores 0-10 with higher scores indicating more pain interference

Change in pain severityBaseline, 4 weeks, 8 weeks, 12 weeks

Measured using Brief Pain Inventory Short Form (BPI-SF), scores 0-10 with higher scores indicating more pain severity

Change in painDaily up to 12 weeks

Assessed using Pain, Enjoyment of Life and General Activity Scale (PEG Scale), scores 0-10 with higher scores indicating more pain

Change in daily use of prescription opioidsDaily up to 12 weeks

Assessed using self-reported number of prescription opioids taken in last 24 hours

Secondary Outcome Measures
NameTimeMethod
Change in quality of lifeBaseline, 4 weeks, 8 weeks, 12 weeks

Assessed using Linear Analog Scale Assessment, scores 0-10, higher scores indicating better quality of life

Change in mental health statusBaseline, 4 weeks, 8 weeks, 12 weeks

Assessed using Patient Health Questionnaire-4 (PHQ-4), scores 0-12, higher scores indicating severe anxiety and depression

Change in sleep qualityBaseline, 4 weeks, 8 weeks, 12 weeks

Assessed using Insomnia Severity Index (ISI), scores 0-28, higher scores indicating more severe insomnia

Side effects of medical cannabisBaseline, 4 weeks, 8 weeks, 12 weeks

Assessed using sum of side effects self-reported, higher scores indicating higher rates of side effects

Trial Locations

Locations (1)

Thomas Jefferson University Hospital

🇺🇸

Philadelphia, Pennsylvania, United States

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