Tools for the Differential Diagnosis of Fibromyalgia Based on Cognitive Tasks

Sponsor
National Council of Scientific and Technical Research, Argentina (Other)
Overall Status
Recruiting
CT.gov ID
NCT05910372
Collaborator
Center for Nuclear and Molecular Medicine Entre Ríos (Other)
28
1
3.2
8.7

Study Details

Study Description

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

Condition or Disease Intervention/Treatment Phase
  • Other: Color Comparison Task
  • Other: N-back Task

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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
28 participants
Observational Model:
Case-Control
Time Perspective:
Cross-Sectional
Official Title:
Development of Complementary Tools for the Differential Diagnosis of Fibromyalgia Based on Cognitive Task Performance
Actual Study Start Date :
Apr 25, 2023
Anticipated Primary Completion Date :
Aug 1, 2023
Anticipated Study Completion Date :
Aug 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Fibromyalgia Patients

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.

Other: Color Comparison Task
Participants are presented with a series of colored squares and are instructed to compare the colors of two sequentially presented stimuli.

Other: N-back Task
Participants are presented with a sequence of letters and they must indicate whether the current stimulus matches the one presented 2 steps back in the sequence.

Healthy Controls

Volunteers with no clinical history of chronic pain, musculoskeletal or articular disorders.

Other: Color Comparison Task
Participants are presented with a series of colored squares and are instructed to compare the colors of two sequentially presented stimuli.

Other: N-back Task
Participants are presented with a sequence of letters and they must indicate whether the current stimulus matches the one presented 2 steps back in the sequence.

Outcome Measures

Primary Outcome Measures

  1. 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

  1. Fibromyalgia Impact Questionnaire-Revised version (FIQR) [10 minutes before the intervention]

    Instrument for the assessment and evaluation of fibromyalgia patient's status

  2. 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.

  3. Hospital Anxiety and Depression Scale (HADS) [10 minutes before the intervention]

    Widely used instrument to evaluate anxiety and depression

  4. 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.

  5. Power in EEG bands [Immediately after the intervention]

    Analysis of EEG spectrum bands

  6. Event-related potentials amplitude [Immediately after the intervention]

    Amplitude, in microvolts, of event-related brain potentials

  7. Event-related potentials latency [Immediately after the intervention]

    Latency, in milliseconds, of event-related brain potentials

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
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.

Exclusion Criteria:
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Center for Nuclear and Molecular Medicine Entre Ríos (CEMENER) Oro Verde Entre Ríos Argentina 3100

Sponsors and Collaborators

  • National Council of Scientific and Technical Research, Argentina
  • Center for Nuclear and Molecular Medicine Entre Ríos

Investigators

  • Principal Investigator: José A Biurrun Manresa, PhD, National Council of Scientific and Technical Research, Argentina (CONICET)

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
José Biurrun Manresa, PhD in Biomedical Science and Engineering, National Council of Scientific and Technical Research, Argentina
ClinicalTrials.gov Identifier:
NCT05910372
Other Study ID Numbers:
  • IS003981
First Posted:
Jun 18, 2023
Last Update Posted:
Jun 18, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by José Biurrun Manresa, PhD in Biomedical Science and Engineering, National Council of Scientific and Technical Research, Argentina
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 18, 2023