Tracking pain and related outcomes using technology
Using Technology to Track Pain and Pain-related Outcomes
This study is testing a new mobile app designed to help people with chronic pain track their symptoms and medications to see if it can improve their self-management.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 21 Years and up |
| Sex | All |
| Sponsor | Johns Hopkins University Academic / other |
| Locations | 1 site (Baltimore, Maryland) |
| Trial ID | NCT04267588 on ClinicalTrials.gov |
What this trial studies
This observational study aims to develop a mobile app that helps patients track their chronic pain, medications, and related symptoms. By engaging with patients at a clinic, the researchers will gather feedback and pilot test the app to ensure it meets the needs of those suffering from chronic pain. The study addresses the significant public health issue of chronic pain, which affects millions and is often complicated by sleep disturbances and psychiatric disorders. The goal is to create a cost-effective, accessible self-management tool for chronic pain patients.
Who should consider this trial
Good fit: Ideal candidates are adults aged 21 and older with chronic pain lasting more than three months and an average pain level above 3 out of 10.
Not a fit: Patients with cognitive impairments, unstable psychiatric disorders, or those currently abusing substances may not benefit from this study.
Why it matters
Potential benefit: If successful, this technology could empower patients to better manage their chronic pain and improve their quality of life.
How similar studies have performed: Other studies have shown promise in using technology for pain management, but this specific approach is innovative and tailored to chronic pain self-management.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ≥ 21 years of age * Pain duration \> 3 months * Average pain level of \>3 out of 10 (0=no pain; 10=worst pain imaginable) * English fluency * Are not scheduled to undergo any medical procedures during the course of the study * Have a physician-confirmed medical diagnosis associated with chronic pain * Are willing to comply with the study protocol and give written informed consent. Patients taking non-narcotic analgesics must be on a stable dose one month prior to participation. Exclusion Criteria: * Delirium, dementia, or cognitive impairment (i.e., Mini Mental State Exam score \<24) * Unstable major psychiatric disorder or history of schizophrenia * Beck Depression Inventory score \>30 or report of suicidal ideation * Active substance abuse; * Refusal to provide access to relevant medical record information.
Where this trial is running
Baltimore, Maryland
- Behavioral Medicine Research Lab — Baltimore, Maryland, United States (Recruiting)
Study contacts
- Principal investigator: Luis F Buenaver, Ph. D — Johns Hopkins University
- Study coordinator: Luis F Buenaver, PhD
- Email: lbuenav1@jhmi.edu
- Phone: 410-550-7000
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.