Assessing the Impact of the Personalized Medicine Clinic on Mental Health Outcomes
1 other identifier
observational
200
0 countries
N/A
Brief Summary
We are trying to find out if personalized dosing of antidepressant medications using information gathered at the Personalized Medicine Clinic can improve patients' mental health. The main question it aims to answer is if the Personalized Medicine Clinic can improve depressive symptoms based on the CES-D survey score.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2026
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 15, 2026
CompletedFirst Posted
Study publicly available on registry
May 22, 2026
CompletedStudy Start
First participant enrolled
July 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2028
Study Completion
Last participant's last visit for all outcomes
June 1, 2028
May 22, 2026
May 1, 2026
1.9 years
May 15, 2026
May 15, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
CES-D Survey Score
CES-D survey score is a 20-item self-reported questionnaire that was designed to assess depressive symptoms. The score is from 0-60 with higher numbers indicating greater depressive symptoms.
From enrollment to 6 months
Study Arms (1)
Personalized Medicine Cohort
Patients referred to the Personalized Medicine Clinic for guidance on antidepressant therapy.
Interventions
Personalized Medicine Clinic services with specific focus on pharmacogenetic recommendations and patient education.
Eligibility Criteria
Adult patients referred to the Personalized Medicine clinic for genotype-guided drug dosing and selection related to mental health pharmacotherapy as part of clinical care.
You may qualify if:
- Depressive symptoms
You may not qualify if:
- Patients who do not speak English, patients with severe mental illness including hospitalized patients or patients with suicidal ideation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Clinical Pharmacologist
Study Record Dates
First Submitted
May 15, 2026
First Posted
May 22, 2026
Study Start (Estimated)
July 1, 2026
Primary Completion (Estimated)
June 1, 2028
Study Completion (Estimated)
June 1, 2028
Last Updated
May 22, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share