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Recruiting NCT06288282

Behavioral and Cognitive Predictors of Persistent Pain and Opioid Misuse in Chronic Pain

Observational Chronic Back Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: No Intervention.
Who it may be relevant to
Registry conditions: Chronic Back Pain. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Chronic lower back pain (CLBP) affects approximately 20% of the global population. The study objective is to determine if impulsivity, inhibitory control, drug choice, and/or cognitive distortions predict opioid misuse and disability in patients with chronic pain. This is a prospective consented cross-sectional study characterizing behavioral and cognitive phenotypes using both patient-reported survey measures and cognitive testing. Outcome measures include correlations between impulsivity measures, opioid drug choice responses and cognitive distortion scores, and risk for opioid misuse (Primary outcomes: COMM scores, SOAPPR scores). Secondary outcomes is BPI measurement. A Certificate of Confidentiality will provide additional protections for participants.

Interventions

  • Other No Intervention
    No intervention will be used.

Primary outcome measures

  • Screener and Opioid Assessment for patients with pain revised (SOAPPR) [Time frame: within 12 months]
  • Current Opioid misuse measure (COMM) surveys [Time frame: within 12 months]
Secondary outcome measures (1)
  • Pain Intensity with Brief Pain inventory (BPI) [Time frame: within 12 months]

Eligibility criteria

Inclusion criteria

  • With diagnoses related to chronic lower back pain
  • Age above 18yrs
  • Non pregnant

Exclusion criteria

  • Cancer pain

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • Mount Sinai Pain management centers — New York

Identifiers

NCT: NCT06288282 · STUDY-23-01287

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗