eurofeedback for Fibromyalgia.
- Conditions
- FibromyalgiaNeurological - Other neurological disorders
- Registration Number
- ACTRN12623000244606
- Lead Sponsor
- niversity of Otago
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 30
Participants with a diagnosis of fibromyalgia will be eligible to participate.
To be included in the study, participants must meet all of the following inclusion criteria:
•Capable of understanding and signing an informed consent form
•Age between 18 to 75 years on the day of the consent
•Satisfy the Modified American Collage of Rheumatology (ACR) 2011 Fibromyalgia Diagnostic Criteria
•A score greater than or equal to 4 on the 11-point numeric pain rating scale (NPRS, 0=No pain to 10=Worst pain) in the past 7 days
•A disability score of greater than or equal to 50 on Fibromyalgia Impact Questionnaire
Participants who meet any of the following conditions will be excluded:
•Neurological conditions
•Cognitive and psychiatric disorders
•Epilepsy
•Seizures
•Substance abuse
•Pregnant or six-months post-partum
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Brief pain inventory-short form[Baseline, immediately post-completion of intervention, and at follow-up of 10 days and 1-month post-completion of intervention];Arthritis Impact Questionnaire[Baseline, immediately post-completion of intervention, and at follow-up of 10 days and 1-month post-completion of intervention];Fibromyalgia Impact Questionnaire[Baseline, immediately post-completion of intervention, and at follow-up of 10 days and 1-month post-completion of intervention]
- Secondary Outcome Measures
Name Time Method