Mental Processes for Rating Pain Intensity
1 other identifier
observational
44
1 country
1
Brief Summary
This new study builds on the principal investigator's earlier studies to improve communication about pain. The research team seeks to better understanding of the mental processes needed to rate pain.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Nov 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 3, 2024
CompletedStudy Start
First participant enrolled
November 11, 2024
CompletedFirst Posted
Study publicly available on registry
February 12, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 20, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 20, 2025
CompletedFebruary 12, 2025
February 1, 2025
6 months
November 3, 2024
February 11, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
pain intensity
Pain intensity is the severity or magnitude of perceived pain. The researchers will use a 0 ("no pain")-10("pain as bad as you can imagine") numeric rating scale.
3 weeks
Interventions
observational
Eligibility Criteria
Community sample
You may qualify if:
- years old or older;
- visited a HCP for treatment of a painful musculoskeletal condition within previous year;
- has usually felt, at least, "mild" musculoskeletal pain on most days of the last 3 months in multiple locations; and
- has felt variable musculoskeletal pain intensity during the last 3 months.
You may not qualify if:
- past or current employment as a licensed healthcare provider;
- diagnosed with a cardiac arrhythmia;
- has a battery-powered implant in the neck, chest, abdomen, or spine (e.g., pacemaker);
- diagnosed with a neurological condition that causes uncontrolled movement (e.g., Parkinsonism, epilepsy, etc.);
- smokes cigarettes or vapes; (6) has abused substances during the last week; or
- allergic to skin adhesives.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Missouri
Columbia, Missouri, 65211, United States
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assoc Prof
Study Record Dates
First Submitted
November 3, 2024
First Posted
February 12, 2025
Study Start
November 11, 2024
Primary Completion
May 20, 2025
Study Completion
May 20, 2025
Last Updated
February 12, 2025
Record last verified: 2025-02