Actively Recruiting
Prediction of Antidepressant Effects of Electroconvulsive Therapy
Led by Medical University of Vienna · Updated on 2025-09-25
30
Participants Needed
1
Research Sites
208 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Despite its successful use for more than 80 years, the mechanisms of action of electroconvulsive therapy (ECT) are still not fully understood. ECT has been shown to be accompanied by changes in regional brain volumes and connectivity measures, as well as biochemical alterations. However, how these changes relate to ECT response remains to be further elucidated; up to now, there are no objective markers for the targeted use of ECT in clinical practice. Methods: Study design: longitudinal mono-centre study with duration of 36 months. Subjects: 30 depressed patients (aged 18-65 years) eligible for ECT. Measurements: subjects will undergo 2 3-Tesla MRI scans (one before and one after a course of ECT), including structural MRI, resting-state functional MRI, task-based functional MRI and MR spectroscopy. Blood, CSF sampling and clinical assessments will be performed once before and once after the ECT course. ECT: Each patient will be treated in a min. of 8 bitemporal ECT sessions (\~4 weeks). Data analysis: Longitudinal changes in brain imaging parameters and laboratory measures (before/after ECT) will be assessed using repeated-measures analysis of covariance. Machine learning with random forests will be employed to identify a pattern of pretreatment imaging, biochemical (serum and CSF) and clinical parameters that are best qualified to predict response to ECT as defined by a reduction of ≥50% of baseline HAMD17. Hypotheses: 1. ECT will be accompanied by changes in brain morphology, functional connectivity, neuronal activation in response to cognitive and reward-related stimuli and neurochemical signals in the brain. 2. ECT leads to changes in blood- and CSF-based markers of neuronal plasticity, neurodegeneration and inflammation, as well as genetic/epigenetic markers. 3. Predictive markers of ECT response can be established based on the relationships between imaging, neurochemical and clinical markers and treatment response. Innovation: This study would be the first to combine multimodal MRI measures with the assessment of biomarkers in the CSF in the context of ECT. The implementation of the proposed trial represents an important step towards a better understanding of the powerful antidepressant properties of ECT. By relating treatment effects and potentially underlying biological mechanisms on numerous complementary levels, the study might help to identify biomarkers that distinguish patients who are likely to benefit from ECT from non-responders. Ultimately, results of the study might be useful in order to establish an individualized medical indication for ECT.
CONDITIONS
Official Title
Prediction of Antidepressant Effects of Electroconvulsive Therapy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female inpatients aged 18 to 65 years
- Diagnosis of severe unipolar depression according to ICD-10 codes F32.2, F32.3, F33.2, or F33.3
- Baseline HAMD17 score of 23 or higher
- Physically healthy
- Ability and willingness to provide written informed consent
- Negative drug screening and negative urine pregnancy test for women
- Stable antidepressant and antipsychotic medication for at least 10 days before inclusion
- Anesthesiological approval for electroconvulsive therapy
You will not qualify if you...
- Severe somatic or neurological disease
- Current comorbid psychiatric disorders including bipolar depression
- Past or current schizophrenia or schizoaffective disorder
- Current use or abuse of alcohol, drugs, or medications indicating chronic abuse or substance dependence
- Clinically relevant abnormalities on physical exam or routine labs
- Pregnancy or breastfeeding
- Contraindications to lumbar puncture such as increased intracranial pressure or bleeding disorders
- Any implant or metal graft that is incompatible with MRI
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Department of Psychiatry and Psychotherapy, Medical University of Vienna
Vienna, Austria, 1090
Actively Recruiting
Research Team
P
Pia Baldinger-Melich, MD, PhD, PD, Assoc.Prof.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here