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ProCAN clinical trial for CHR

The purpose of this study is to determine if the MT1988 study medication can improve memory, clinical symptoms, and other biomarkers in participants at a clinical high risk (CHR) for psychosis.

Age & Gender

  • 17 years ~ 30 years
  • Male, Female, Gender Inclusive

Visit Availability

  • Standard business hours (M-F, 8-5)
  • Extended hours (M-F, early morning or evening)

Location

North Carolina (Statewide)

What will be asked of you

At each study visit you will meet with a study team member and complete symptom interviews and memory tasks. This study will involve up to 6 blood draws, 5 urine samples, 3 EKGs, 3 EEGs, and willingness to take the study medication regularly.

Incentives

Up to $1500, study medication and optional psychoeducation

In-person visits:
10
Phone or online visits:
1-3
Total length of participation:
3 months

Looking for Healthy Volunteers

Requirements for healthy volunteers are different than for those with a specific condition. If you are interested in becoming a healthy volunteer for this study, use the below categories to determine if you are able to participate.

Able to participate:

  • Meet diagnostic criteria for CHR as determined by a study clinician.
  • Not pregnant and not planning to become pregnant for at least 4 months after study enrollment.
  • Willing and able to complete scheduled visits, treatment plan, lab tests, and other study procedures.

Not eligible if:

  • A history of schizophrenia or psychosis spectrum disorders, including bipolar disorder or a major neurocognitive disorder resulting from a TBI.
  • Have already participated in a clinical trial related to cognition in the last 3 months.

Contact the Team

Visit Location

Contact & Visit Location

Primary Contact

Visit Study Website

Primary Visit Location

Medical School Wing B (UNC-Chapel Hill)
332 Emergency Room Dr, Chapel Hill, NC 27514, USA

Additional Study Information

Principal Investigator

Diana Perkins
Psychiatry - Center of Excellence - Outreach and Support Intervention Services (OASIS)

Study Type

Clinical or Medical
Interventional

Study Topics

Mental and Emotional Health

IRB Number

25-2359

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