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Depression Paid Clinical Trials in New York
A listing of 49 Depression clinical trials in New York actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
25 - 36 of 49
The state of New York currently has 49 active clinical trials seeking participants for Depression research studies. These trials are conducted in various cities, including New York, Rochester, Bronx and Buffalo.
Featured Trial
Major Depressive Disorder Clinical Study
Recruiting
Is depression weighing you down? Local major depressive disorder clinical studies are now enrolling participants in the area. Participating in research studies helps contribute to the advancement of future medicine and treatment options. There is no obligation to take part and health insurance is not required.
Conditions:
Major Depressive Disorder
Major Depression
Major Depressive Episode
Major Depressive Disorder (MDD)
Major Depressive Disorders
Featured Trial
Bipolar Disorder Study (Medicare Required)
Recruiting
Non-drug Bipolar Depression study for adults with Medicare. If you have Bipolar Disorder, are over the age of 18, and are currently depressed, you may be eligible to take part in this study. If you have tried at least four treatments and not found them helpful, you are a good candidate for this study. All study-related care will be provided at no cost to you.
Conditions:
Bipolar Disorder
Bipolar Depression
Bipolar I Disorder
Depression
Bipolar
Featured Trial
Hyperacusis Activities Treatment-Online Study
Recruiting
Are you experiencing hyperacusis? If so, we are recruiting adults with hyperacusis to complete a clinical trial supported by the National Institutes of Health. The study involves participating in a remote counseling program and sound therapy trial for hyperacusis, Hyperacusis Activities Treatment-Online.
Conditions:
Hyperacusis
Tinnitus
Hearing Loss
Featured Trial
Paid Clinical Studies Nationwide
Recruiting
Nationwide clinical trials offered in your area. Some trials offering up to several thousand dollars in compensation for participation.
Mobile Cognitive Behavioral Therapy for Medical and Graduate Students
Recruiting
The study aims to assess and compare clinician-delivered cognitive behavior therapy (CBT) supplemented with "MAYA", a mobile cognitive behavioral therapy app program to clinician-delivered cognitive behavioral therapy alone. The experimental group will be asked to use the mobile application at least two times per week for six weeks, for at least 20 minutes on each of the two days in addition to the clinician-delivered CBT. Participants will complete a weekly self-report assessment battery design... Read More
Gender:
All
Ages:
Between 18 years and 40 years
Trial Updated:
12/11/2023
Locations: Weill Cornell Medical College, New York, New York
Conditions: Anxiety Disorders, Depression
Psychiatric Outcomes of Unruptured Intracranial Aneurysms (POUIA)
Recruiting
The impact of cerebrovascular procedures on patients experiencing anxiety and depression is not well studied despite the high prevalence of these mental health disorders. Unruptured Intracranial aneurysms (UIAs) have a prevalence of approximately 3% and an annual risk of 1-2% in the general population. Despite the high risk of fatality following aneurysm rupture with a rate of 40-50%, the overall aneurysm growth and rupture risks are rare (less than 3% per aneurysm per year) and many patients ca... Read More
Gender:
All
Ages:
Between 18 years and 75 years
Trial Updated:
12/04/2023
Locations: Montefiore Medical Center, Bronx, New York
Conditions: Anxiety Depression, Aneurysm Cerebral, Mental Health Wellness 1
Trajectories of Recovery After Intravenous Propofol Versus Inhaled VolatilE Anesthesia Trial
Recruiting
The investigators will conduct a 12,500-patient randomized multi-center trial to determine (i) which general anesthesia technique yields superior patient recovery experiences in any of three surgical categories ((a) major inpatient surgery, (b) minor inpatient surgery, (c) outpatient surgery) and (ii) whether TIVA confers no more than a small (0.2 %) increased risk of intraoperative awareness than INVA in patients undergoing both outpatient and inpatient surgeries
Gender:
All
Ages:
18 years and above
Trial Updated:
11/22/2023
Locations: Weill Cornell Medicine, New York, New York
Conditions: Surgery-Complications, Anesthesia Complication, Anesthesia Awareness, Anesthesia, Surgery, Quality of Life, Pain, Postoperative, Anesthesia Morbidity, Depression, Sleep Disorders, Circadian Rhythm
Brief Interventions for Coping With Distress
Recruiting
This study is being done to compare the effectiveness of three different skills trainings to cope with distress. These three trainings are: 1) an attention skills training, 2) an attention and reflective thought skills training, and 3) a health and wellness education training.
Gender:
All
Ages:
Between 18 years and 65 years
Trial Updated:
11/21/2023
Locations: Teachers College, Columbia University, New York, New York
Virtual Reality at End-of-life
Recruiting
The purpose of this research is to determine the effect that repeated, personalized virtual reality experiences have on symptom severity, comparing self-reported symptom severity both pre and post each session, and overtime across sessions. We will also determine if this intervention results in a high rating of presence in VR, and if presence is related to the magnitude of the change in symptoms.
Gender:
All
Ages:
All
Trial Updated:
11/20/2023
Locations: Hospice and Palliative Care Buffalo, Cheektowaga, New York
Conditions: End of Life, Pain, Nausea, Fatigue, Well-Being, Psychological, Depression, Dyspnea, Appetite Loss, Anxiety
Safe Mothers, Safe Children Initiative
Recruiting
The purpose of this study is to assess the efficacy of the combined interventions, Skills Training in Affective and Interpersonal Regulation (STAIR) and Parent-Child Interaction Therapy (PCIT) or P-STAIR, for treating maternal PTSD and reducing maltreatment recidivism.
Gender:
Female
Ages:
18 years and above
Trial Updated:
11/15/2023
Locations: McSilver Institute for Poverty Policy and Research, New York, New York
Single-dose Ketamine Treatment to Improve Depression in Mild Cognitive Impairment
Recruiting
Ketamine is a NMDA-receptor antagonist that promotes synapse formation and has been shown to rapidly improve symptoms in depression. Even a single dose of ketamine has been shown to improve depression and cognition with short-term memory, inhibitory control, cognitive flexibility, and processing speed showing improvements within days of treatment. The mechanism behind ketamine's rapid action is not clear but some groups have speculated it may be related to enhanced neuroplasticity, particularly... Read More
Gender:
All
Ages:
Between 50 years and 90 years
Trial Updated:
10/23/2023
Locations: Icahn School of Medicine at Mount Sinai (Depression and Anxiety Center), New York, New York
Conditions: Depression, Mild Cognitive Impairment
Engage & Connect: A Psychotherapy for Postpartum Depression
Recruiting
This study tests a novel psychotherapy, Engage & Connect, tailored to reduce postpartum depression. The study includes 9 weeks of psychotherapy, delivered remotely. It will examine changes in social isolation, processing of social rewards and depression severity over 9 weeks of treatment.
Gender:
Female
Ages:
All
Trial Updated:
10/19/2023
Locations: Weill Cornell Medicine, New York, New York
Conditions: Postpartum Depression
Tele-PROTECT Therapy: Effectiveness, Empowerment, and Implementation
Recruiting
The purpose of this randomized trial is to conduct a fully powered effectiveness trial of video-delivered PROTECT (Tele-PROTECT) compared to a video-delivered depression education (DepEd) control condition to be delivered to 140 English- and Spanish-speaking NYC elder abuse victims. Investigators hypothesize three main aims:
Effectiveness Aim: Tele-PROTECT participants will have significantly greater and clinically meaningful reductions in depression when compared to the DepEd control;
Abuse Im... Read More
Gender:
All
Ages:
60 years and above
Trial Updated:
10/19/2023
Locations: Weill Cornell Medicine, New York, New York
Conditions: Depression, Elder Abuse
DBS for TRD With the Medtronic Percept PC
Recruiting
Of the estimated 30 million Americans who suffer from Major Depressive Disorder, approximately 10% are considered treatment resistant. Deep brain stimulation (DBS) to a region of the brain called the subcallosal cingulate (SCC) is an emerging strategy for treatment resistant depression (TRD), which involves placement of electrodes in a specific region of the brain and stimulating that area with electricity. This is believed to reset the brain network responsible for symptoms and results in a sig... Read More
Gender:
All
Ages:
Between 25 years and 70 years
Trial Updated:
10/11/2023
Locations: Icahn School of Medicine at Mount Sinai, Mount Sinai West, New York, New York
Conditions: Major Depressive Disorder, Treatment Resistant Depression
Feasibility and Acceptability of a Novel Cognitive Behavioral Skills Mobile App for Pregnant and Postpartum Individuals
Recruiting
This study aims to assess the feasibility and acceptability of the Maya Perinatal Cognitive Behavioral Skills App, a novel app for pregnant and postpartum individuals experiencing difficulties with mood, anxiety, or stress. Participants will complete the 12-module app to learn evidence-based strategies previously shown to help manage mood and anxiety. Assessments will include app feedback questionnaires, feedback interviews, a daily symptom tracker, and symptom measures. The study investigators... Read More
Gender:
Female
Ages:
18 years and above
Trial Updated:
09/29/2023
Locations: Weill Cornell Medical College, New York, New York
Conditions: Perinatal Anxiety, Perinatal Depression
Treatment of Post-partum Depression Using an Behavioral Intervention Called ROSE (Reach Out, Stay Strong, Essentials for Mothers of Newborns) Delivered Using an Electronic App
Recruiting
A randomized trial of pregnant people at risk for postpartum depression comparing the InBloom app (n = 76) to ROSE (n = 76; weekly scheduled group), and two control groups. We will assess Depression at baseline and 1, 2 and 3 months, ROI at 3 months, Satisfaction at 1 and 3 months and Perceived Access at 1 and 3 months. Subject participation will last up to 8 months (minimum 17 weeks pregnant through 3 months postpartum).
Gender:
Female
Ages:
18 years and above
Trial Updated:
09/26/2023
Locations: University of Rochester Medical Center, Rochester, New York
Conditions: Post-partum Depression
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