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Study identifier: NCT07116109 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Neuromodulation + Prolonged Exposure Therapy: Evaluation of a Technology-Enhanced, Integrated Treatment for Pain and PTSD

Condition: Chronic Pain · Post Traumatic Stress Disorder (PTSD)  ·  Sponsor: The University of Texas Health Science Center, Houston

PhaseNA
Planned participants146
Who can joinAll sexes, 21 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to examine comparative effectiveness of two home-based telemedicine delivered interventions: transcranial Direct Current Stimulation (tDCS) combined with Massed Prolonged Exposure (Massed-PE) vs. Sham tDCS combined with Massed PE, focusing on pain and PTSD outcomes, to determine the comparative effectiveness of the two interventions on process outcomes of patient satisfaction, treatment attrition, and treatment compliance and to explore changes in blood biomarkers associated with stress and inflammatory processes related to pain and PTSD symptom improvements following treatment.

This description comes directly from the study's public registry record.

Talk to the study team

Melba Hernandez-Tejada, PhD, DHA  ·  713 4862729  ·  Melba.A.HernandezTejada@uth.tmc.edu

Stephanie Hart  ·  843-577-5011 x205103  ·  zeigls@musc.edu

Always discuss trial participation with your own doctor first.

Locations (2)

Charleston VA Healthcare SystemCharleston, South Carolina, United StatesRecruiting
The University of Texas Health Science Center at HoustonHouston, Texas, United StatesActive Not Recruiting

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Source record: clinicaltrials.gov/study/NCT07116109