Tools for the Differential Diagnosis of Fibromyalgia Based on Cognitive Tasks
- Conditions
- Fibromyalgia
- Interventions
- Other: Color Comparison TaskOther: N-back Task
- Registration Number
- NCT05910372
- Lead Sponsor
- National Council of Scientific and Technical Research, Argentina
- Brief Summary
The goal of this observational study is to test for behavioural and neurophysiological biomarkers in fibromyalgia patients. The main questions it aims to answer are:
* Is there a measurable decline in working memory?
* Could these measures help in fibromyalgia differential diagnosis?
Participants will:
* perform Color Comparison tasks
* perform n-back tasks
- Detailed Description
Fibromyalgia is a disease characterized by the presence of generalized musculoskeletal pain, accompanied by non-specific symptoms such as depression, sleep disturbances, anxiety, cognitive disabilities, among others. While widespread musculoskeletal pain is the predominant symptom in patients with fibromyalgia, cognitive impairments have also been widely reported, including decreased ability to concentrate, decreased short-term memory, and inability to multitask, which differentiate fibromyalgia patients from those with other chronic pain syndromes. Specifically, quantitative evidence has been found of impairment in executive functions in this group of patients, particularly in the domains of inhibitory control and working memory.
In the present study, participants (both healthy individuals and those diagnosed with fibromyalgia) will perform two cognitive tasks designed to assess the capacity and retrieval of information from working memory. The first task is the Color Comparison task, in which colored squares will appear on a computer screen for a short period of time. After a blank delay, a new set of squares will appear, and a decision has to be made about whether or not the squares are the same as the ones shown first. The task will be divided into 10 blocks of 30 trials each, with 10 trials comparing 2 colored squares, 10 trials comparing 4 colored squares, and 10 trials comparing 6 colored squares. A resting period will be given between each block. The behavioral results of this task will include reaction times and hit rates. At the same time, electroencephalographic data will be recorded to evaluate the Contralateral Delay Activity (CDA). The amplitude of this waveform is linked to the number of items allocated in working memory.
The second task that will be carried out by the participants is the n-back task. A sequence of letters will be presented, and participants will be asked to indicate whether the current stimulus matches the one presented two stimuli earlier. Sixty-two stimuli will be presented per block, and 5 blocks will be carried out. The results will be analyzed in terms of behavioral analysis and Event-Related Potentials (ERPs) analysis.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
Fibromyalgia patients:
- Primary diagnosis of fibromyalgia according to the criteria used by the healthcare professional in charge of the patient.
- Other comorbidities are accepted as long as the pain caused by them is less severe than the pain caused by fibromyalgia.
- Willingness and ability to fully understand the content and scope of the experiment and to comply with the experiment instructions.
- Normal or corrected-to-normal vision.
Healthy controls:
- No history of neurological diseases, chronic pain or musculoskeletal disorders.
- Willingness and ability to fully understand the content and scope of the experiment and to comply with the experiment instructions.
- Normal or corrected-to-normal vision.
Fibromyalgia patients:
- Pregnancy
- History of addictive behavior, defined as alcohol, cannabis, opioids or other drugs abuse.
- Presence of fever, tuberculosis, malignant tumors, infectious processes, acute inflammatory processes.
- Lack of cooperation
Healthy controls:
- Pregnancy
- History of chronic pain or musculoskeletal or articular disorders
- History of addictive behavior, defined as alcohol, cannabis, opioids or other drugs abuse.
- Presence of fever, tuberculosis, malignant tumors, infectious processes, acute inflammatory processes.
- Lack of cooperation
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Fibromyalgia Patients N-back Task Patients with primary fibromyalgia diagnosis. May include other chronic pain comorbidities, but the pain associated with those diseases should be less severe than the pain caused by fibromyalgia. Fibromyalgia Patients Color Comparison Task Patients with primary fibromyalgia diagnosis. May include other chronic pain comorbidities, but the pain associated with those diseases should be less severe than the pain caused by fibromyalgia. Healthy Controls Color Comparison Task Volunteers with no clinical history of chronic pain, musculoskeletal or articular disorders. Healthy Controls N-back Task Volunteers with no clinical history of chronic pain, musculoskeletal or articular disorders.
- Primary Outcome Measures
Name Time Method Percentage of correct answers in the Color Comparison task Immediately after the intervention Percentage of correct answers over total number of trial in the Color Comparison Task
- Secondary Outcome Measures
Name Time Method Symptoms Impact Questionnaire (SIQ) 10 minutes before the intervention Instrument to assess healthy control's status regarding relevant clinical symptoms experienced in the last week.
Power in EEG bands Immediately after the intervention Analysis of EEG spectrum bands
Fibromyalgia Impact Questionnaire-Revised version (FIQR) 10 minutes before the intervention Instrument for the assessment and evaluation of fibromyalgia patient's status
Brief Pain Inventory-Short Form (BPI-SF) 10 minutes before the intervention It is an instrument to assess the severity of pain and its impact on functioning.
Hospital Anxiety and Depression Scale (HADS) 10 minutes before the intervention Widely used instrument to evaluate anxiety and depression
Event-related potentials amplitude Immediately after the intervention Amplitude, in microvolts, of event-related brain potentials
Event-related potentials latency Immediately after the intervention Latency, in milliseconds, of event-related brain potentials
Trial Locations
- Locations (1)
Center for Nuclear and Molecular Medicine Entre Ríos (CEMENER)
🇦🇷Oro Verde, Entre Ríos, Argentina