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Not yet recruiting NCT07601477

Assessing the Impact of the Personalized Medicine Clinic on Mental Health Outcomes

— Observational Mental Health Depressive Disorder Pharmacogenetic Testing Antidepressant

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Personalized Medicine Clinic.
Who it may be relevant to
Registry conditions: Mental Health, Depressive Disorder, Pharmacogenetic Testing, Antidepressant. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The aim of this study is to investigate 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.

Interventions

  • Other Personalized Medicine Clinic
    Personalized Medicine Clinic services with specific focus on pharmacogenetic recommendations and patient education.

Primary outcome measures

  • CES-D Survey Score [Time frame: From enrollment to 6 months]

Eligibility criteria

Inclusion criteria

  • Depressive symptoms

Exclusion criteria

  • Patients who do not speak English
  • Patients with severe mental illness including hospitalized patients or patients with suicidal ideation

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07601477 · 128940

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗