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35 Years
experience
Innovative Mental Health Clinical Trials in Princeton, NJ
Princeton Medical Institute has been at the forefront of clinical research in mental health and neurology since 1989. Our 12,000-square-foot facility in Central New Jersey is staffed by board-certified physicians, registered nurses, and experienced clinical research professionals. Over 5,000 patients have participated in more than 500 clinical trials at our site, which opened in 1991. We collaborate with pharmaceutical companies to evaluate investigational medications for conditions like Alzheimers disease, depression, and bipolar disorder.

As a member of the Global Alzheimers Platform, we bridge academic research and community healthcare. Our team includes globally recognized experts, including Dr. Jeffrey Apter, who has published over 30 articles in psychiatric and Alzheimers research. We prioritize patient safety, ethical standards, and advancing treatments for chronic conditions.
Services
Alzheimer's Disease Trials Depression Clinical Studies Bipolar Disorder Research Generalized Anxiety Trials Social Anxiety Studies Binge Eating Disorder Trials Hypersomnia Research Memory Loss Evaluations Smoking Cessation Studies PTSD Clinical Trials
Details
  • Year established: 1991
Highlights and features
  • We have enrolled over 5,000 patients in 500+ clinical trials since 1991.
  • Our team includes board-certified physicians and published Alzheimers researchers.
  • We offer free evaluations and access to investigational treatments not yet available.
  • Partnerships with pharmaceutical companies ensure cutting-edge research opportunities.
  • Conveniently located in Central New Jersey near Princeton University.
Services
Alzheimer's Disease Trials
Our Alzheimers disease trials evaluate investigational drugs to improve safety and efficacy for patients aged 5085. Participants receive free medical assessments and study medication. The research aims to advance treatments through phases of clinical evaluation.
Depression Clinical Studies
Depression studies focus on treatment-resistant cases, testing new medications combined with psychological support. Eligible participants undergo free evaluations and may receive compensation for time and travel during the 62-week study period.
Social Anxiety Research
Social anxiety disorder trials recruit adults aged 1865 to test investigational medications. The study includes free clinical evaluations and procedures, with potential compensation for qualified participants seeking alternative treatments.
Bipolar Disorder Research
Bipolar disorder studies assess new therapies for mood swings and emotional instability. Participants receive free study-related care and access to investigational drugs, with eligibility determined through initial screenings.
Memory Loss Evaluations
Free memory loss evaluations identify early signs of cognitive decline. The program targets individuals experiencing significant memory deterioration, offering access to clinical trials focused on intervention and long-term management.
People
Dr. Jeffrey T. Apter
Founder & Lead Principal Investigator
Dr. Apter founded Global Medical Institutes and leads Princeton Medical Institutes research. He has collaborated with Princeton University on Alzheimers research and published over 30 peer-reviewed articles in psychiatric and neurology fields.
Questions
What is clinical research?
Clinical research evaluates the safety and efficacy of new medications, devices, or treatments through human trials to advance medical knowledge and patient care.
What is a clinical trial?
A clinical trial tests new medical approaches on volunteers to determine if they are safe and effective for treating or preventing diseases.
Why should I volunteer for a study?
Volunteering provides access to investigational treatments, free medical assessments, and contributes to medical advancements for future patients.
Do I need insurance to participate?
No insurance is required. All study-related costs are covered by the trial sponsor.
Are there risks in clinical trials?
Risks vary by study and are outlined in the informed consent document before participation begins.
Can I leave a trial early?
Yes, participants may withdraw from a trial at any time without penalty or loss of benefits.