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Search / Trial NCT03626142

Assessing the Effectiveness of Psychiatric Interventions on the Inpatient Unit

Launched by STANFORD UNIVERSITY · Aug 7, 2018

Trial Information

Current as of November 14, 2025

Enrolling by invitation

Keywords

ClinConnect Summary

This Stanford University study is watching how well three treatments work for people on the psychiatric inpatient unit who have depressive symptoms or suicidal thoughts. It’s an observational study, meaning researchers observe real-world outcomes after people receive one of three interventions: accelerated theta burst stimulation to the left dorsolateral prefrontal cortex (Left DLPFC aTBS), accelerated theta burst stimulation to the anterior cingulate cortex (ACC aTBS), or electroconvulsive therapy (ECT). The main goal is to see how depressive symptoms change over time and how safe and acceptable these treatments are in everyday care.

Who can join? Adults 18 and older who are admitted to Stanford Hospital’s psychiatric unit for depressive symptoms or suicidal ideation and who have received one of the three listed interventions. There are no other listed exclusion criteria. After discharge, participants will be followed for up to 6 months, with weekly mood and symptom check-ins for the first 4 weeks and then every two weeks up to 24 weeks. They’ll complete several assessments of depression and suicidal thoughts (for example, MADRS and SSI) plus other mood and sleep measures, and researchers will track medication changes and any hospital readmissions. The study, which started in 2018, aims to enroll about 200 people and will not share individual data.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Received an intervention on the psychiatric inpatient unit at Stanford Hospital aimed at treating a major depressive episode or suicidal ideation
  • Exclusion Criteria:
  • -None

About Stanford University

Stanford University is a prestigious academic institution renowned for its cutting-edge research and innovation in healthcare and medicine. As a clinical trial sponsor, Stanford leverages its extensive resources, including a collaborative network of world-class researchers and state-of-the-art facilities, to advance medical knowledge and improve patient care. The university is committed to conducting rigorous, ethical research that adheres to the highest standards of scientific integrity, fostering an environment where groundbreaking discoveries can translate into effective clinical applications. Through its clinical trials, Stanford aims to address critical health challenges and contribute to the development of novel therapies and treatment strategies.

Locations

Palo Alto, California, United States

Patients applied

0 patients applied

Trial Officials

Nolan Williams, MD

Principal Investigator

Stanford University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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