Northwestern University
Chicago, Illinois, 60611, United States
NCT Number: NCT05669924
This work aims to study the neural correlates and determinants of pain dynamics related to changes in a noxious stimulus.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 2
Chicago, Illinois, 60611, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
-
Exclusion criteria
0.35 mg/kg methylphenidate will be administered after baseline testing and 45 min-1 hr before post-intervention testing.
Placebo for methylphenidate
Time frame: 6 months
We will compare acute pain dynamics-i.e., the time series of pain visual analog scale ratings (0-100, where 0 = no pain and 100 = worst pain imaginable) obtained while delivering a changing noxious stimulus-during the methylphenidate condition to that of the placebo condition.
Time frame: 6 months
We will regress the time course of nucleus accumbens BOLD activity onto the latent time series obtained from our valence competition model. This will be supported by regressing the nucleus accumbens time course onto the pain VAS time course, allowing our findings to be compared to standard analyses in the literature.
Northwestern University
Other
The Neural Correlates of and Effects of Methylphenidate on Acute Pain Dynamics
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