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Establishment of a registry for multimodal monitoring of patients treated with electroconvulsive therapy (ECT) and other stimulation and treatment methods (rTMS, VNS, other treatments)

Establishment of a registry for multimodal monitoring of patients treated with electroconvulsive therapy (ECT) and other stimulation and treatment methods (rTMS, VNS, other treatments) - MModStim

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00038040
Enrollment
600
Registered
2025-10-13
Start date
2025-10-30
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients suffering from unipolar or bipolar depression, schizoaffective disorder, or schizophrenia

Interventions

Group 1: Patients who are treated with electroconvulsive therapy (ECT group) As part of the establishment of a registry for multimodal monitoring, various parameters are collected (in both study arms
Elektrika, Inc.). c) Self- and observer-rated assessments are used to measure symptom severity, level of functioning, and quality of life. Childhood trauma is also assessed. d) Assessment of cognitive

Sponsors

Uniklinik RWTH Aachen, Klinik für Psychiatrie, Psychotherapie und Psychosomatik
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: All patients suffering from unipolar or bipolar depression, or a schizoaffective disorder, or schizophrenia, and - who are to be treated with electroconvulsive therapy (ECT group), or - who are to be treated with other stimulation and treatment methods (repetitive transcranial magnetic stimulation, vagus nerve stimulation, or other treatments without neurostimulation) (control group)

Exclusion criteria

Exclusion criteria: - Patients who are not capable of giving consent - Patients who are hospitalized against their will - Pregnancy - Minor patients - Patients who do not have the required language skills

Design outcomes

Primary

MeasureTime frame
Exploratory study aimed at hypothesis generation without predefined endpoints. This is an exploratory study aimed at identifying new patterns and relationships in order to generate new hypotheses regarding the mechanism of action of the treatment, the pathophysiology of the disorder, predictors of response, and the course of illness.

Secondary

MeasureTime frame
Exploratory study aimed at hypothesis generation without predefined endpoints.

Countries

Germany

Contacts

Public ContactErhan Kavakbasi

Uniklinik RWTH Aachen, Klinik für Psychiatrie, Psychotherapie und Psychosomatik

ekavakbasi@ukaachen.de+49 241 80 89640

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 10, 2026