Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06667674

A Swedish Internet CBT for Prolonged Grief Disorder: a Three-armed RCT

Led by Uppsala University · Updated on 2025-04-29

270

Participants Needed

2

Research Sites

166 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to evaluate the effectiveness of internet-delivered Cognitive Behavioral Therapy (iCBT) in reducing symptoms of prolonged grief in adults diagnosed with prolonged grief disorder. The main questions the study aims to answer are: * Does iCBT reduce symptoms of prolonged grief disorder, posttraumatic stress, and depression following the death of a loved one in the short and long term? * What mechanisms contribute to the effectiveness of iCBT in treating prolonged grief disorder? The iCBT intervention will be compared to a waitlist control group and an active control group to see if iCBT reduces symptoms of prolonged grief disorder more effectively than no treatment or a placebo treatment. Participants will: * Be randomly assigned to either the iCBT group, an active control group or a waitlist control group * Complete online assessments of symptom severity, grief cognitions, and level of avoidance before, during and after intervention * Engage in 10 weeks of a therapist-guided online treatment

CONDITIONS

Official Title

A Swedish Internet CBT for Prolonged Grief Disorder: a Three-armed RCT

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Currently residing in Sweden
  • Lost a relative or close friend to any cause of death at least six months ago
  • Diagnosed with prolonged grief disorder
Not Eligible

You will not qualify if you...

  • Having severe psychiatric problems that may interfere with treatment or need urgent care, such as untreated psychotic disorder, untreated bipolar disorder, ongoing substance abuse, or high suicide risk
  • Changed dosage of mental health medication in the past four weeks or planning a change in the next two months

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Region Uppsala, KBT via nätet, Nära vård digitalt

Uppsala, Sweden, 751 85

Actively Recruiting

2

Uppsala university, Dep of Womens and Childrens Health

Uppsala, Sweden, 75185

Actively Recruiting

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Research Team

J

Josefin Sveen, Professor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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