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Spatiotemporal Thalamocortical Alterations Underlie Experimental and Chronic Pain

RecruitingHealthy volunteers welcome

Spatiotemporal Thalamocortical Alterations Underlie Experimental and Chronic Pain - Phase II

Who can join

Ages 18 to 60 · All sexes · Healthy volunteers welcome

Full eligibility criteria
Inclusion Criteria:

* Meet the MRI / EEG screening criteria
* Fluent in English

Exclusion Criteria:

* Current or history of major medical, neurological, or psychiatric illness based on self-report
* History of cardiac, respiratory, or nervous system disease that, in the investigator's judgment, precludes participation in the study because of a heightened potential for adverse outcome (for example: asthma or claustrophobia)
* History of head trauma
* Pregnant or lactating
* Presence of any contraindications to MRI scanning (for example: cardiac pacemaker, metal implants, claustrophobia, pregnancy, cannot lie still in fMRI scanner)
* Conditions making study participation difficult (e.g., paralysis, psychoses, or other severe psychological problems as per the judgment of a study investigator during Session 1)
* Active substance abuse disorders (based on subject self-report)

About the study

The purpose of this study is to assess thalamocortical (TC) connectivity during tonic pressure pain, to evaluate alpha activity during tonic pressure pain and to determine pressure pain ratings by using Electroencephalography (EEG), Functional Magnetic Resonance Imaging (fMRI), Transcranial Alternating Current Stimulation (tACS), sham and Transcranial random noise stimulation (tRNS)

What is being tested

Sponsor: The University of Texas Health Science Center, Houston · Participants: 60 · Started: Jun 1, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT06968689

Locations in the U.S.

TexasThe University of Texas Health Science Center at Houston, Houston

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.