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PTSD · Philadelphia

PTSD clinical trials in Philadelphia

2 recruiting posttraumatic stress disorder studies within range of Philadelphia. Click any trial for full eligibility criteria and contact info.

A Mechanistic Trial of the Neurobiology of Extinction Learning and Intraparietal Sulcus Stimulation

NCT06234969 · Posttraumatic Stress Disorder
Recruiting

This study will be the first of its kind to explore the impact of continuous theta burst stimulation (cTBS) to the intraparietal sulcus (IPS) on arousal symptoms among patients with posttraumatic stress disorder (PTSD). The investigators will demonstrate that IPS cTBS results in significant reduction in arousal (measured by startle response) compared to sham cTBS, that IPS cTBS interacts with extinction training to further improve arousal, and that there is a dose/response effect of cTBS on arousal. The investigators will also demonstrate that IPS cTBS significantly improves retention of extinction learning, the experimental analogue of exposure therapy.

PhaseNA
TypeInterventional
Age18 Years – 60 Years
WherePhiladelphia, Pennsylvania, United States
SponsorUniversity of Pennsylvania
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RISE Versus Advocacy-based Enhanced Care as Usual for Patients Experiencing IPV

NCT06906302 · Intimate Partner Violence (IPV)
Recruiting

This study aims to improve treatment for Veterans Health Administration (VHA) patients who experience intimate partner violence (IPV). This study will evaluate two brief counseling interventions for VHA patients who have experienced IPV in the past 12 months: Recovering from IPV through Strength and Empowerment (RISE) and advocacy-based Enhanced Care as Usual (ECAU). The RISE intervention includes up to 8 sessions and includes specific topic areas (e.g., social support, health effects, resources). The other intervention, ECAU, includes a single session that includes supportive education about IPV and health effects, discussion of ways to increase safety, and information about resources. This study will test which approach is better for improving self-efficacy and other aspects of health. Participants will answer surveys about their self-efficacy and other health and safety indicators (e.g., mental health symptoms) right before receiving treatment, approximately 12 weeks later, and then every three months after that for one year. Participation in this research will last about 15 months.

PhaseNA
TypeInterventional
Age18 Years
WhereBoston, Massachusetts, United States + 2 more
SponsorBoston University
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