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Patient preferences for receiving an early intervention after critical illness to improve psychological recovery

Patient preferences for receiving an early intervention after critical illness to improve psychological recovery

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615001079538
Acronym
PRINCIPLE
Enrollment
60
Registered
2015-10-14
Start date
2016-08-18
Completion date
2018-03-20
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Survivors of critical illness experience significant physical, psychological and cognitive compromise during recovery. ICU diaries have been proposed as one intervention that may be effective in helping survivors recover psychological function. Despite support by some members of the intensive care community, there is a lack of empirical work investigating diaries and subsequent concern regarding the potential harm of such an intervention exists. This study is designed to determine feasibility of two proposed psychological interventions for survivors of critical illness: (1) the use of ICU diaries and (2) the provision of an individualised summary of the ICU experience prepared by ICU staff and based on the User Centred Critical Care Discharge Information. The effect size of each psychological intervention to reduce psychological compromise (anxiety, depression, posttraumatic stress symptomatology) will also be determined to inform sample size calculations for a larger efficacy randomised control trial. Other aims of this pilot study are to determine the feasibility of early screening for psychological health for survivors of critical illness, and to validate the Intensive Care Psychological Assessment Tool (IPAT) against recognised depression and anxiety screening instruments in an Australian ICU population.

Interventions

Intensive Care Unit (ICU) diary intervention: in addition to standard care participants will receive a narrative account of their clinical condition and progress prepared jointly by the ICU staff and family members throughout the patient’s ICU stay. The ICU diary will be retained by ICU staff when the participant is discharged to the ward and will be provided to the participant when she/he indicates readiness to receive the diary (between five days and three months after ICU discharge). The diar

Intensive Care Unit (ICU) diary intervention: in addition to standard care participants will receive a narrative account of their clinical condition and progress prepared jointly by the ICU staff and family members throughout the patient’s ICU stay. The ICU diary will be retained by ICU staff when the participant is discharged to the ward and will be provided to the participant when she/he indicates readiness to receive the diary (between five days and three months after ICU discharge). The diary will be given to the patient in the form of a booklet containing narrative text from staff and family members. The patient will be made aware of the diary 5 days post ICU discharge or as soon after as possible when they are in the hospital wards. The diary will be checked for appropriateness prior to being given to the patient. The number of entries will be monitored (as this is a pilot study). Individualised care intervention: provision of an individualised summary of the ICU experience prepared by ICU staff and based on the User Centred Critical Care Discharge Information. The ICU experience summary will include the following information: reason for ICU admission, date of ICU admission, length of ICU stay, how the patient arrived to the ICU (by ambulance, transferred from another hospital, family member or friend brought them, etc.), discharge location (medical ward, surgical ward, home, etc.) and a summary of the important elements of the patient’s ICU journey such as the patient’s diagnosis, treatments and procedures. This summary will be given to the participant in hospital after consenting, and when each participant considers he or she is ready to receive the information. Each participant will be followed up with at least one telephone call 2 weeks post hospital discharge. The purpose of the telephone call is to discuss any problems that the patient may be experiencing and attempt to address these. The ICU Registered Nurse or Research Assistant (with training from psychologist) will perform the phone call. Additional strategies that will be available to the participant include a supported visit to ICU, discussion of challenges the participant is currently experiencing, psychological counselling and provision of detailed information outlining additional support options available. The information regarding the additional support options available will be provided as part of the telephone call and individualised written information.

Sponsors

Princess Alexandra Hospital
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

Patients: Consecutive patients who meet the inclusion/exclusion criteria will be invited to participate. Inclusion criteria: 1. ICU patients with expected ICU LOS >48 hours 2. Able to speak and understand English 3. Glasgow Coma Scale (GCS) 14 – 15 prior to leaving ICU 4. Expected survival beyond hospital (in consultation with the ICU clinical team) of at least 1 month Family members: Family members of the patients who meet the above inclusion criteria will be invited to participate in the study. Clinicians: Clinicians who care for patients in the intensive care and have been involved in contributing to the ICU diary or the ICU discharge summary will be invited to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Patients who are not able to receive the intervention or be followed up post discharge (e.g. overseas patients, prisoners) 2. Patients with active psychotic impairment of a history of organic impairment

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 28, 2026