Development of assistive system for recording symptoms of chronic pain and investigation of pain exacerbation factors
Not Applicable
- Conditions
- Chronic pain
- Registration Number
- JPRN-UMIN000022543
- Lead Sponsor
- Okayama University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who are unable to operate information input devices from some reasons, such as severe pain or motor disturbance, are excluded. There is no key exclusion criteria for healthy person.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method We implement several interfaces as a part of the assistive system for recording symptoms of chronic pain and their related data. These interfaces are composed of smart devices, input devices and wearable devices. Primary outcome is the usability of these interfaces for integrating into the system. The usability of these interfaces is evaluated by questionnaires and interviews with participants.
- Secondary Outcome Measures
Name Time Method The promising cause of chronic pain exacerbation factors will be analyzed after four to twelve weeks system use, by contrast with the questionnaires and the change in the other related data (e.g. atmospheric pressure). These are correlated by date and time. Key secondary outcome is results in recording data analysis. The results are associated with the relationship between an exacerbation of pain and its factors, and between the exacerbation and the degree of environmental factor changes.