TrialPath
Anxiety · New York

Anxiety clinical trials in New York

5 recruiting anxiety disorder studies within range of New York. Click any trial for full eligibility criteria and contact info.

The Effects of Daily Polyvagal Exercises on Stress in Students of Physical Therapy

NCT06557083 · Stress, Anxiety
Recruiting

The purpose of this study is to investigate whether specific breathing exercises can stimulate the polyvagal system and thus decrease stress in healthy students of physical therapy. The hypothesis is that practicing daily polyvagal breathing exercises will result in decreased stress/anxiety in physical therapy students compared to the control group who will not be receiving any intervention.

PhaseNA
TypeInterventional
Age18 Years – 45 Years
WhereOrangeburg, New York, United States
SponsorDominican University New York
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Helping Adults With Obsessive-Compulsive Disorder Succeed at Work

NCT07124780 · Obsessive-Compulsive Disorder (OCD)
Recruiting

The purpose of this study is to compare two models of employment services for people with obsessive-compulsive disorder (OCD) interested in finding and maintaining employment. All 40 participants will receive up to 12 sessions of the first-line treatment for OCD called exposure and response prevention, a form of Cognitive Behavioral Therapy (CBT). Assigned by chance, half of the people will also receive Individual Placement and Support (IPS); the other half will receive standard vocational services (SVS). This study will compare these two approaches for helping adults with OCD find and maintain work.

PhaseNA
TypeInterventional
Age18 Years – 60 Years
WhereNew York, New York, United States
SponsorNew York State Psychiatric Institute
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Prevention of Psychological Health Problems Via Integrated Operational Support

NCT06981598 · Depression, Anxiety, Grief, Leadership
Recruiting

Sub-clinical behavioral health services in the military are performed by BH technicians, who receive minimal training. Due to this, embedding more technicians in military units is unlikely to benefit service members. Giving technicians training in, and access to, evidence-based interventions (EBI) could make their work more effective. The proposed study is a training trial examining the efficacy of the full integrated operational support (IOS) toolkit (evidence-based interventions for behavioral health), relative to routine care using standard resources, as a prevention resource for active-duty airmen.

PhaseNA
TypeInterventional
Age18 Years
WhereNew York, New York, United States
SponsorNew York University
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ERP to Improve Functioning in Veterans With OCD

NCT05240924 · Obsessive Compulsive Disorder (OCD), Comorbid Post-Traumatic Stress Disorder and OCD
Recruiting

Obsessive compulsive disorder (OCD) is a debilitating psychiatric illness impacting work, social, and family functioning. Exposure and Response Prevention (ERP) is the sole evidence-based psychotherapy for OCD; however, no randomized controlled trials (RCTs) have examined the effectiveness of ERP among Veterans or individuals with both OCD and posttraumatic stress disorder (PTSD). This 4-year Hybrid Type I trial will compare outcomes of ERP to those of a control condition among Veterans with OCD. Primary and secondary aims will examine whether Veterans' functioning, quality of life, and OCD symptoms differ between the ERP and control in the full sample of Veterans with OCD, and in the half of the sample with both OCD and PTSD. The tertiary aim is to conduct a mixed-methods formative evaluation of the implementation potential of ERP in VA mental health settings.

PhaseNA
TypeInterventional
Age18 Years
WhereEast Orange, New Jersey, United States + 17 more
SponsorVA Office of Research and Development
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Pramipexole to Enhance Social Connections

Recruiting

This study seeks to understand if the medication pramipexole improves social connectedness and functioning in adults (ages 18-50) who experience anxiety or depression. The study plans to enroll 108 participants total across two sites (University of California San Diego and New York State Psychiatric Institute). Pramipexole will be given in a 6-week randomized, double-blind, placebo-controlled trial. Social reward processing will be assessed using measures of brain function (fMRI), behavior, and self-report at baseline and week 6. Knowledge gained from this study will help determine the therapeutic potential of targeting the dopamine system to remediate social disconnection as an anxiety and depression intervention.

PhasePhase 2
TypeInterventional
Age18 Years – 50 Years
WhereSan Diego, California, United States + 1 more
SponsorUniversity of California, San Diego
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