Trauma and Stressor Related Disorders Clinical Trials
2 recruiting trials for Trauma and Stressor Related Disorders. Eligibility criteria explained in plain English.
TrialFinderData lists 2 Trauma and Stressor Related Disorders clinical trials drawn from ClinicalTrials.gov, all of which are currently recruiting participants.
Research is led by Dartmouth-Hitchcock Medical Center (1), University of Guelph (1), among the most active sponsors registered for these trials.
The most frequently studied intervention is Trauma-Focused Cognitive Behavioral Therapy, modified for autistic youth (behavioral, 1 trial), followed by Modular Approach to Therapy for Children with Anxiety, Depression, Trauma or Conduct Problems.
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Recruiting Trials
Clinical trial data sourced from the ClinicalTrials.gov registry, maintained by the National Library of Medicine. Always consult your doctor before considering any clinical trial.
TF-CBT for Autistic Youth Pilot Implementation - Open Pilot
Compared to the general population, autistic youth are at increased risk for both exposure to potentially traumatic events and trauma-related symptoms following trauma exposure....
Big Feelings: A Study on Children's Emotions in Therapy
The goal of this clinical trial is to learn about how psychotherapy works for children and adolescents aged 8 - 15 with anxiety, depression, trauma, or disruptive behaviour. The...
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Frequently Asked Questions
There are currently 2 clinical trials for Trauma and Stressor Related Disorders, with 2 actively recruiting participants. These include trials across all phases from early-stage Phase 1 to late-stage Phase 3.
To join a clinical trial for Trauma and Stressor Related Disorders, review the eligibility criteria on the trial detail pages, then talk to your doctor about whether a trial is right for you. Your doctor can help you evaluate the potential benefits and risks.
Phase 3 trials are large-scale studies that test whether a treatment is effective and monitor side effects. There are 0 Phase 3 trials for Trauma and Stressor Related Disorders, representing treatments closest to potential FDA approval.
Clinical trials follow strict safety protocols overseen by Institutional Review Boards (IRBs) and the FDA. Participants are monitored closely and can withdraw at any time. Always discuss risks and benefits with your healthcare provider before enrolling.
Trial data sourced from the ClinicalTrials.gov API. This site does not provide medical advice, always talk to your doctor about clinical trial participation.