Participation Studies

This page provides people living with mental illness, their families, and mental health researchers with an opportunity to connect in mental health research studies.

NAMI-NYC Metro does not endorse any study on this page. Information is provided purely as a public service.

A group wishing to post on this page must submit their current IRB approval for the study, in addition to a written synopsis of your study answering the following:

  • Include a brief description of the study.
  • Is the study therapeutic (offering treatment) or non-therapeutic?
  • Is the study funded? If yes, provide source of all funding; e.g., non-profit organization, governmental agency, or for-profit corporation including any ties to the pharmaceutical industry.
  • Who will be conducting the study? E.g. non-profit, government, hospital, or for-profit corporation, including any companies that run clinical trials.
  • Will subjects be paid? Include payment schedule and amount.

Current Studies

September 2016: The Role of Dysmyelination in Cognitive Impairment of Psychotic Spectrum Disorders

NYU Langone Medical Center-Radiology

The purpose of this study is to investigate whether differences in white matter in the brain are related to cognitive performance in young people diagnosed with schizophrenia, schizoaffective disorder, and bipolar disorder. We are also looking for siblings without a diagnosis to participate.

The study involves:
Phone screen
Diagnostic interview ($40)
Blood draw ($40)
MRI ($40)
Cognitive assessment ($40)
Total for participation in all parts of study: $160

For more information please contact:

Christine Stepanek:, 646-501-4600

August 2016: Genomic Psychiatry Cohort Study: Schizophrenia, Bipolar Disorder

We are currently seeking individuals 18 years or older diagnosed with schizophrenia or bipolar disorder to take part in a genetics study at NYU School of Medicine. The study’s purpose is to investigate the genetic risks associated with these chronic mental illnesses.

The study involves a brief screening questionnaire, a diagnostic interview, two short questionnaires asking about your history of trauma and aggression, and a blood draw of no more than 4 tablespoons. The study should take 2-3 hours to complete and you will be compensated $50 in cash.

If you are interested in participating, please contact Mara at or by phone at (646) 754-4817 between the hours of 9:30am-5pm MondayFriday.

March 2016: Intravenous Sodium Nitroprusside in Adults with Symptomatic Schizophrenia

NYU Langone Medical Center – Schizophrenia Research Lab

The purpose of this study is to find out if sodium nitroprusside, when given intravenously (into a vein) can help reduce various symptoms of schizophrenia, compared to a placebo. Current treatments for schizophrenia may require weeks to produce a therapeutic effect, and other efforts to find better-tolerated treatments have not met much success.


  • 18-60 years old
  • Diagnosis of schizophrenia
  • Currently treated with an antipsychotic


  • Study involves 9 visits (2 infusions)
  • Up to $840.00 for participation

For more information, please contact:
Erica Diminich, PhD

January 2016: Rutgers University Research Study: Tele-Psychiatry Intervention to Improve Engagement in, and Outcomes from, Family Psychoeducation for Serious Mental Illness

Seeking Caregivers for Individuals Diagnosed with Schizophrenia, Schizoaffective Disorder, or Bipolar Disorder

We are currently recruiting for a study of the effects of various family support programs for those who are the primary caregiver for someone diagnosed with a serious mental illness.


  • Residing in the New Jersey, New York, or Philadelphia area
  • Access to computer or tablet with internet
  • Participants and their loved ones must be over the age of 18 and be in contact with each other 2-3x per week or living together


  • Study involves 3 phone interview appointments
  • Participants receive $10 per phone appointment

For more information or to sign up as a participant, please contact our research assistant:
Victoria Martin
Rutgers UBHC
151 Centennial Avenue
Piscataway NJ 08854
Tel: 732-235-5098

December 2015: Ketamine Plus Lithium as a Novel Pharmacotherapeutic Strategy in Treatment-Resistant Depression

Icahn School of Medicine at Mount Sinai

The purpose of this study is to test the antidepressant effect of ketamine when given repeatedly over a period of 1 week, as well as the use of Lithium as a relapse-prevention strategy for patients with treatment-resistant depression (TRD) who respond to an initial ketamine infusion. An additional purpose of this study is to research the effects of ketamine on brain function.

Compensation per each visit listed below:

  • Screening (including medical clearance): $50
  • Ketamine infusion (1 visit): $60
  • 24 hour follow-up visit/lithium randomization visit: $20
  • Baseline fMRI: $200
  • Continuation ketamine Infusions (3 visits): $180
  • fMRI scan following first infusion: $200
  • Weekly clinic visits (up to 6): $120
  • fMRI scan 2 weeks following last infusion: $100
  • Total for completion of all phases of the study: $930

For more information, please contact:

Jaclyn Schwartz,, 212-241-3116

December 2015: Cognitive Training for Mood and Anxiety Disorders

Icahn School of Medicine at Mount Sinai

The primary objective is to investigate the efficacy of a novel cognitive training computer program in treating depression and anxiety. The training program seeks to improve working memory and attention in addition to alleviating depressive and anxious symptoms.

Compensation per each visit listed below:

  • Screening visit 1 (initial interview): $25
  • Baseline assessment: $50
  • Weekly clinician check-ins (5 x $20 each): $100
  • Mid-study assessment (including week 3 check-in): $40
  • Final assessment: $50
  • Total for participation in all parts of the study: $265

For more information, please contact:

Megan Hoch:, 212-241-3089

December 2015: Randomized Controlled Trial of Repeated Dose Intravenous Ketamine for PTSD

Icahn School of Medicine at Mount Sinai

The purpose of this study is to study new ways to treat post-traumatic stress disorder (PTSD). Current treatments for PTSD do not work for everyone and it can take time to determine whether a person responds to a chosen treatment. The purpose of this study is to see whether ketamine, when given repeatedly intravenously (into a vein) can produce a quick and persistent improvement in PTSD symptoms, compared to the active control of midazolam.

Compensation per each visit listed below:

  • Screening: $75
  • First MRI scan (Friday before first administration): $100
  • Visit 1a (Monday of first administration): $75
  • Visit 1b (24 hour): $50
  • Second MRI scan (also 24 hour): $100
  • Visit 2 (Second administration): $50
  • Visit 3 (Third administration): $50
  • Week Two administrations (visits 4-6): $175
  • Visit 7 (exit): $50
  • Study Visits Total, including two scans: $725
  • Follow-up phase (*weekly for one month, monthly for 6 months): $25/visit

For more information, please contact:

Sarah Horn:, 212-241-7910

September 2015: D-Cycloserine Augmentation of Cognitive Behavioral Therapy for Delusions

NYU Langone Medical Center – Schizophrenia Research Lab.

Have you been diagnosed with Schizophrenia, Schizoaffective or Delusional Disorder?

We are looking for volunteers between the ages of 18-68 years old interested in participating a weekly research study.

Up to $400.00 in compensation for participation.

Brief Summary

The purpose of this study is to investigate if D-cycloserine (DCS) along with once-weekly CBT sessions can help individuals with treatment-resistant delusions. This study aims to help increase mental flexibility and memory for information learned during CBT sessions.

Learn more about the study here.

For more information, please contact:
Erica Diminch Ph.D

June 2015: Psychosis Biomarker Study

Columbia University Child Psychiatry Dept.

The Columbia University Child Psychiatry Department is conducting a psychosis biomarker study, investigating the underlying causes of psychosis, specifically immune and infectious causes. We are recruiting those ages 8-35 who have experienced psychosis, as well as unaffected siblings of those with psychosis. The study involves an approximate 2 hour clinical assessment and requires a blood draw and a urine sample.

Participant Eligibility criteria includes:

  • Ages 8-35
  • Experienced psychosis in the past or currently
  • Also recruiting unaffected siblings of those with psychosis, ages 8-35

Study participants will receive a cash stipend of $25.

For more information, please contact:
Shannon Delaney, MD (Please include “Psychosis Biomarker Study” in the subject line.)