NCT06822764

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

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
44

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Nov 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 3, 2024

Completed
8 days until next milestone

Study Start

First participant enrolled

November 11, 2024

Completed
3 months until next milestone

First Posted

Study publicly available on registry

February 12, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 20, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 20, 2025

Completed
Last Updated

February 12, 2025

Status Verified

February 1, 2025

Enrollment Period

6 months

First QC Date

November 3, 2024

Last Update Submit

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

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Location

MeSH Terms

Conditions

Pain

Interventions

Watchful Waiting

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Outcome Assessment, Health CareOutcome and Process Assessment, Health CareQuality of Health CareHealth Services Administration

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

Locations