Actively Recruiting

Age: 21Years +
All Genders
NCT04267588

Using Technology to Track Pain and Pain-related Outcomes

Led by Johns Hopkins University · Updated on 2025-06-29

100

Participants Needed

1

Research Sites

307 weeks

Total Duration

On this page

Sponsors

J

Johns Hopkins University

Lead Sponsor

P

PainCare, LLC

Collaborating Sponsor

AI-Summary

What this Trial Is About

Persistent pain is a public health epidemic. The current protocol seeks to develop technology to aid patients' tracking of patients' pain, medications and pain-related variables. The investigators seek to talk with patients in co-investigator's clinic to solicit feedback, as well as pilot test the technology with pain patients.

CONDITIONS

Official Title

Using Technology to Track Pain and Pain-related Outcomes

Who Can Participate

Age: 21Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 21 years of age or older
  • Pain lasting more than 3 months
  • Average pain level greater than 3 out of 10
  • Fluent in English
  • Not scheduled for any medical procedures during the study
  • Physician-confirmed medical diagnosis related to chronic pain
  • Willing to comply with study protocol and provide written consent
  • Stable dose of non-narcotic analgesics for at least one month before participation
Not Eligible

You will not qualify if you...

  • Delirium, dementia, or cognitive impairment (Mini Mental State Exam score less than 24)
  • Unstable major psychiatric disorder or history of schizophrenia
  • Beck Depression Inventory score greater than 30 or suicidal thoughts
  • Active substance abuse
  • Refusal to allow access to relevant medical records

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Behavioral Medicine Research Lab

Baltimore, Maryland, United States, 21224

Actively Recruiting

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Research Team

L

Luis F Buenaver, PhD

CONTACT

L

Luis F Buenaver, Ph. D

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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