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The role of attention in endogenous pain control

Completed
Conditions
fibromyalgia
muscle
joint or bone
10028393
Registration Number
NL-OMON35822
Lead Sponsor
niversitair Medisch Centrum Utrecht
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
80
Inclusion Criteria

Patients will have the diagnosis of primary fibromyalgia according to the American College of Rheumatology (ACR) classification criteria. Control participants will be matched on age and educational level to fibromyalgia patients and will be healthy and pain-free as determined by a general health questionnaire, and not take any psychoactive medication or analgesics. All subjects will be adults over the age of 18 years old and speak Dutch fluently.

Exclusion Criteria

The inability to give informed consent, a serious neurological or psychiatric condition besides fibromyalgia, current participation in another research protocol that could interfere or influence the outcome measures of the present study , current use of sedative psychotropic or analgesic drugs (e.g., benzodiazepine, antiepileptics, barbiturates and opioids) except amitriptyline in low dosages (<50 mg/day), or when there is any serious injury to the body regions to be tested as reported by the research participant.

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary study parameter is the effect of attentional modulation on CPM<br /><br>efficacy in patients with fibromyalgia compared to healthy controls. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Secondary parameters are: 1) attentional task performance in patients with<br /><br>fibromyalgia versus healthy controls, 2) associations between CPM efficacy and<br /><br>cognitive inhibition, and 3) sex differences in CPM efficacy and attentional<br /><br>effects in fibromylagia versus healthy controls. </p><br>
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