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Spatiotemporal Thalamocortical Alterations Underlie Experimental and Chronic Pain

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Enrolling

Conditions

Pain

Treatments

Device: transcranial alternating current stimulation (tACS)
Device: Sham
Device: transcranial random noise stimulation (tRNS)

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06968689
HSC-MS-25-0062
5R01NS129059-03 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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)

Enrollment

60 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

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)

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

60 participants in 6 patient groups

tACS then tRNS then sham
Experimental group
Treatment:
Device: transcranial random noise stimulation (tRNS)
Device: Sham
Device: transcranial alternating current stimulation (tACS)
tACS then sham then tRNS
Experimental group
Treatment:
Device: transcranial random noise stimulation (tRNS)
Device: Sham
Device: transcranial alternating current stimulation (tACS)
tRNS then tACS then sham
Experimental group
Treatment:
Device: transcranial random noise stimulation (tRNS)
Device: Sham
Device: transcranial alternating current stimulation (tACS)
tRNS then sham then tACS
Experimental group
Treatment:
Device: transcranial random noise stimulation (tRNS)
Device: Sham
Device: transcranial alternating current stimulation (tACS)
Sham then tRNS then tACS
Experimental group
Treatment:
Device: transcranial random noise stimulation (tRNS)
Device: Sham
Device: transcranial alternating current stimulation (tACS)
Sham then tACS then tRNS
Experimental group
Treatment:
Device: transcranial random noise stimulation (tRNS)
Device: Sham
Device: transcranial alternating current stimulation (tACS)

Trial contacts and locations

1

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Central trial contact

Wen Li, PhD; Jada Malveaux

Data sourced from clinicaltrials.gov

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