About this trial
This functional magnetic-resonance imaging study of the brain will feature a within-subject crossover design to investigate the effects of a placebo cream on painful thermal stimulation rendered upon eight body sites. The investigators aim to 1.) improve the understanding of how the brain represents thermal pain responses somatotopically (i.e., across different body-sites) 2.) to test these brain representations with and without the presence of a pain-targeted placebo intervention, and 3.) to examine how these brain representations change prior to vs. during the delivery of thermal pain. They predict that placebo cream will downregulate the intensity of aversive brain activity representations, and to a lesser degree, sensation and somatotopic representations, both prior to and during painful thermal stimulation.
Eligibility criteria
Qualifiers
Subject must be a volunteer with a minimum age of 18 years and must be able and willing to provide written informed consent.
If female, the subject must be non-lactating, not pregnant, and using a reliable contraception method.
Subject must be able to read and speak English.
Subject must be able to understand and follow the instructions of the investigator and understand all screening questionnaires.
Disqualifiers
If female, pregnancy.
Inability to tolerate the scanning procedures (e.g., claustrophobia).
Metal in body or prior history working with metal fragments (e.g., as a machinist).
Inability to tolerate heat pain applied to the forearm.
Trial design
Treatments tested in this trial
- Placebo Cream
- Control Cream