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Online cognitive behavioral therapy for distress in people who lost a loved one during the corona pandemic: A randomized waitlist-controlled trial

The effectiveness of an online cognitive behavioral therapy for distress in people who lost a loved one during the corona pandemic: A randomized waitlist-controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON24930
Enrollment
52
Registered
2020-10-21
Start date
2020-07-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Persistent Complex Bereavement Disorder, Post Traumatic Stress Disorder, Major Depressive Disorder

Interventions

The online grief-specific unguided CBT is targeted at people with clinically relevant levels of distress (PCBD, PTSD and/or MDD) at least three months after the loss of a loved one. It could therefore
Schut & Stroebe, 2005). The online CBT consists of eight weekly sessions that are tailored to this specific population. Following the Dutch guidelines for grief-specific CBT, central components of the
the story of the loss (and its circumstances) is discussed in detail and the participant is helped to confront stimuli that s/he tends to avoid. The rationale of exposure is described by given example
specific attention is paid to cognitions connected with responsibility/ guilt and fear, that may be elevated follow

Sponsors

Utrecht University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a person must be a family member, spouse or friend of a person who died (whether or not due to the coronavirus) during the COVID-19 pandemic (period March 2020 till current); - the death occurred at least three months earlier; - = 18 years of age; - report clinically relevant symptom-levels of PCBD, PTSD and/or MDD based on telephone interviews.

Exclusion criteria

Exclusion criteria: Participants will be excluded when they do not have access to the internet, do not master the Dutch language and/ or suffer from a psychotic disorder or are suicidal.

Design outcomes

Primary

MeasureTime frame
PCBD symptoms will be assessed with the Traumatic Grief Inventory – Clinician-Administered (Lenferink et al., in prep.).

Secondary

MeasureTime frame
PTSD symptoms will be assessed with the PTSD Checklist for DSM-5 (Blevins, Weathers, Davis, Witte, & Domino, 2015). MDD symptoms will be assessed with the Patient Health Questionnaire (PHQ-9; Kroenke, Spitzer, & Williams, 2001).

Contacts

Public ContactLyanne Reitsma

Utrecht University

l.reitsma@uu.nl06-22299573

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)