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Intensive Care Unit (ICU) Diaries as a Therapeutic Intervention for Post Traumatic Stress Disorder (PTSD) Following Critical Illness

ICU Diaries as a Therapeutic Intervention for Post Traumatic Stress Disorder Following Critical Illness

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00912613
Acronym
RACHEL II
Enrollment
352
Registered
2009-06-03
Start date
2007-07-31
Completion date
2008-12-31
Last updated
2009-06-03

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

Conditions

Post-Traumatic Stress Disorder

Keywords

Critical illness, ICU Diaries, Post Traumatic Stress Disorder, Incidence

Brief summary

The incidence of PTSD post ICU varies from unit to unit, however a significant number of patients have been shown to develop this disorder. Many patients do not recall their stay in ICU properly and yet can clearly recall nightmares, hallucinations or paranoid delusions, which may be very frightening for the patient to recall at a later stage. As yet, no interventional studies have had an impact on the development of PTSD in this population of patients. However, a recent observational multi-centre study suggested that those patients receiving a diary of their time in ICU had lower levels of symptoms of PTSD than those who did not. These results need to be verified in the form of a randomized study.

Interventions

ICU Diary containing daily information of patients condition and treatment with appropriate photographs

Sponsors

St Helens & Knowsley Teaching Hospitals NHS Trust
CollaboratorOTHER
Vrinnevishuset, Sweden
CollaboratorUNKNOWN
Università degli Studi di Ferrara
CollaboratorOTHER
University of Copenhagen
CollaboratorOTHER
Haukeland University Hospital
CollaboratorOTHER
Hospital Pedro Hispano
CollaboratorOTHER
Sahlgrenska University Hospital
CollaboratorOTHER
General Hospital of Santo António
CollaboratorOTHER
University of Liverpool
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients staying on the ICU for at least 72 hours (with greater than 24 hours of artificial ventilation)

Exclusion criteria

* ICU stay \< 72 hours * Too confused for informed consent * Pre-existing psychotic illness

Design outcomes

Primary

MeasureTime frame
Diagnosis of Post Traumatic Stress Disorder3 months post critical illness

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 30, 2026