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RecruitingNCT05388461

Follow-up after ECT for severe or resistant depression

An observational study follows outcomes, side effects and relapse after ECT received in routine care.

Observational follow-upAges 18+Norway
The study in practice

Understand this study

What is this study about?

This observational registry follows short- and longer-term outcomes after electroconvulsive therapy (ECT), including response, side effects, cognition and relapse.

Who could participate?

Adults treated with ECT for a depressive episode at Haukeland or Stavanger University Hospital after 2013, who give written consent to the regional registry.

What will I do during this study?

People receiving ECT (electroconvulsive therapy) in routine care can consent to the research registry. Patients and clinicians assess depressive symptoms and cognitive function during follow-up.

Listed locations
Bergen and 1 more locationSee all locations and recruitment
Follow-up
6 months of follow-up
Study activities
Patient and clinician assessments

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What to know before participating

Your treatment and care

ECT is received through ordinary clinical care; enrollment in this observational registry does not assign it. Possible cognitive impairment is one of the outcomes being followed.

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateStarted: March 13, 2013
Recruitment status
Recruiting
Enrollment listed in the registry
600
Sponsor
Haukeland University Hospital
Sponsor type
Hospital / academic medical center
Study type
Observational
Intervention type
Other
Locations
Norway
Age range
Over 18 Years
Official registry ID
NCT05388461
Official title
Show the full official title

Acute Efficacy and 6 Months Follow up After Electroconvulsive Therapy for Severe or Treatment Resistant Depression - Predictors of Response, Side Effects, and Relapse

Recruitment & locations

Currently recruiting

Bergen · Stavanger

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Haukeland University Hospital, a hospital or academic medical center.

Who can participate?

Listed age limits: from 18 years.

Is this study still recruiting?

The registry lists this study as recruiting.

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