Acute Efficacy and 6 Months Follow up After Electroconvulsive Therapy

Haukeland University Hospital

Status: Enrolling

Conditions: Depressive Disorder

Treatments: Other: electroconvulsive therapy

Study type: Observational

Funder types: Other

Identifiers

NCT05388461

2018/2541

Details and patient eligibility

About

The overall aim of the current project is to assess the acute and long term outcome of ECT (both patient and clinician rated) in a non-selected patient cohort from ordinary clinical activity, and to seek out factors predicting response and remission, side effects and relapse.

Full description

Patients reffered to electroconvulsive ECT are (after written consent) enroled in a research registry. Based on (clinician and patient rated) measures of depressive symptoms and overall cognitive function, the short and long-term (6 months) efficacy of ECT will be described, and factors predicting response and relapse identified.

The duration of possible cognitive impairment and factors predicting cognitive outcome will be examined.

Enrollment: 600 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients treated with ECT for major depression (F31.3-5, F32, F33) at Haukeland University Hospital or Stavanger University Hospital after 2013,
• written consent to enrolment into the Regional Register for neurostimulation.

Exclusion criteria

• ECT performed on other indications than major depression.
• No consent to the register.