RecruitingNCT05630469

Prediction of Antidepressant Effects of Electroconvulsive Therapy


Sponsor

Medical University of Vienna

Enrollment

30 participants

Start Date

Dec 1, 2022

Study Type

OBSERVATIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This study is trying to identify factors — including brain imaging, blood tests, and spinal fluid analysis — that can predict whether electroconvulsive therapy (ECT) will work for a given patient with severe depression. ECT is a safe and effective treatment that uses brief electrical pulses to trigger a controlled seizure, but it does not work equally well for everyone, and researchers want to understand why. **You may be eligible if...** - You are between 18 and 65 years old - You are a hospital inpatient diagnosed with severe unipolar depression (not bipolar) - Your depression score is severe (HAMD17 ≥23) - You are in physically good health - Your antidepressant medications have been at a stable dose for at least 10 days - You have been approved for ECT by an anesthesiologist **You may NOT be eligible if...** - You have a serious neurological or physical illness - You have another active psychiatric disorder (including bipolar depression or schizophrenia) - You use alcohol, illicit drugs, or other substances in a way consistent with dependence - You are pregnant or breastfeeding - You have contraindications to a lumbar puncture or an MRI scan Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERElectroconvulsive therapy

repetitive induction of a generalized seizure under controlled conditions (muscle relaxation and sedation)


Locations(1)

Department of Psychiatry and Psychotherapy, Medical University of Vienna

Vienna, Austria

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NCT05630469


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