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ICUTogether a web based recovery program for intensive care survivors: a randomised control trial

The Impact of a Mobile Health Intervention on the Mental Health and Wellbeing of Intensive Care Survivors: A Randomised Control Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12618000252213
Acronym
ICUTogether
Enrollment
2
Registered
2018-02-16
Start date
2018-11-23
Completion date
2020-03-16
Last updated
2019-02-04

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

Conditions

None listed

Brief summary

Annually, hundreds of thousands of people survive a life threatening event/illness and require admission to an intensive care unit. Many of those will experience significant and life changing psychological complications as a result. There are no evidence based recovery programs available within Australia or throughout the world which could help reduce the risk of these complications developing. This intervention study will evaluate a mobile health (m-health) recovery program by measuring the emotional and psychological well-being of participants over time. Outcome measures will include incidence and severity of anxiety and depression, Post-Traumatic Stress Disorder and health related quality of life.

Interventions

The intervention is a web based recovery program, available to participants on their smart devices. They will have acess to the web based recovery program for 12 months after discharge. The mobile website will provide information about health and wellbeing during recovery and advice about exercise, sleep and nutrition in this population. Information will be provided about the recovery process per se and also detail the signs and symptoms of maladaptation during recovery and when and how particip

The intervention is a web based recovery program, available to participants on their smart devices. They will have acess to the web based recovery program for 12 months after discharge. The mobile website will provide information about health and wellbeing during recovery and advice about exercise, sleep and nutrition in this population. Information will be provided about the recovery process per se and also detail the signs and symptoms of maladaptation during recovery and when and how participants should seek professional help. The website is not personalised to the participant however they will have access to their own profile page. Participants will be contacted at home via telephone to receive an orientation to the website and the researcher will visit the participant to offer support in initially using the website if required. Participants will be encouraged to journal each day to enable them to reflect on their progress over time but also to explore their thoughts and feelings during recovery however the frequency of use of the website is at the discretion of the participants who will be encouraged to use the site as frequently as they wish. Participants will receive a weekly email summarising their participation over the previous seven days and indicating any days they have not participated along with a prompt to continue participating. Participants will be required to complete a symptom checker each week as well as an electronic journal when they wish to. These and other strategies will make the participants’ interaction with the site more engaging for the duration of the program. On submitting their weekly symptom checker entry an algorithm will be used to determine what message or list of recommended reading the participant will see by the generation of a simple score. An ‘alert’ score can be determined that will trigger an email notification to administrators when any participant submits an entry that reaches a threshold score and therefore gives cause for concern. Participants will not be able to advance through the site unless the symptom checker has been completed at least weekly. A chat room will also be available should participants wish to post items to share with other participants in the study. The chat room will be monitored daily by the researchers who will manage any inappropriate comments by removing them from the chatroom and contacting the participant. The chatroom posts will also help the researchers to identify participants who may be having difficulties and recommend appropriate resources to them based on their posts. An inbuilt trigger word system will also be incorporated into the site to ensure any defamatory or offensive words are identified as soon as they are written and removed from the site.

Sponsors

Joondalup Health Campus
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

Inclusion criteria includes: 1. ventilation in ICU for a minimum period of 24 hours

Exclusion criteria

Exclusion Criteria: 1. Diagnosis of a cognitive impairment either pre-existing or as a result of a critical illness/event

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026