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Real-time Pain Monitoring in Fibromyalgia Patients

NCT03571009 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2018-06-27

No results posted yet for this study

Summary

This study aims to examine whether the pain of fibromyalgia patients can be reduced with utilization of real-time pain monitoring system (PAAS). In this pilot study, adult fibromyalgia patients were randomly assigned to use or to not use PAAS. Changes in the visual analogue scale (VAS) were examined by rheumatologists at baseline and after three months, and correlations between conventional pain VAS or PAAS VAS and clinical parameters (patient global assessment, physician global assessment, fibromyalgia impact questionnaire) were investigated. We also examined if the utilization of PAAS can affect health related quality of life and depression.

Conditions

Interventions

DEVICE

utilization of PAAS

utilization of real-time pain assessment and analysis system (PAAS) consists of wearing device and reporting a real-time pain using the device

Sponsors & Collaborators

  • Ji Hyeon Ju

    lead OTHER

Principal Investigators

  • Ji Hyeon Ju, MD PhD · Seoul St. Mary's Hospital

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-12-22
Primary Completion
2016-11-30
Completion
2017-09-21

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03571009 on ClinicalTrials.gov