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Change of heart rate variability under electroconvulsive therapy

Change of heart rate variability under electroconvulsive therapy - proHECToR

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00035756
Enrollment
50
Registered
2025-02-24
Start date
2025-04-01
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

F32.1

Interventions

Group 1: Observational study: In patients with deprerssive episode undergoing electroconvulsive therapy (ECT) an additional electrocardiogram is performed once after the end of the ECT-series.

Sponsors

RWTH Uniklinik Aachen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Adult patients who are treated as inpatients in the Department of Psychiatry using ECT are treated. The treatment is based on a psychiatric indication and is indication for treatment and is independent of the study. - Signed declaration of consent - Undoubted understanding of the study information

Exclusion criteria

Exclusion criteria: - Persons who are in a dependent / employment relationship with one of the investigators - Inability to comply with the study protocol - Lack of written informed consent - Manifest heart disease

Design outcomes

Primary

MeasureTime frame
The patient's heart rate variability (HRV), determined in the electrocardiogram, after the end of the ECT series. within 3 days after the sixth individual ECT session of the ECT series (T2). Prior to this, an ECG was performed as part of the routine clinical examination before the start of the first ECT, in which the HRV is used as a baseline (T1).

Secondary

MeasureTime frame
Scores determined in the Beck Depression Inventory and (BDI-II) and Hamilton Depression Scale (HAMD) of the patient, after the end of the ECT series. Previously, the BDI-II and HAMD had already been carried out as part of the routine clinical examination before the start of the first ECT, in which the score achieved was used as a basis for comparison.

Countries

Germany

Contacts

Public ContactThomas Frodl

RWTH Uniklinik Aachen

tfrodl@ukaachen.de+492418037550

Outcome results

None listed

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