At a glance
- What the study gets you
- Health checks and monitoring — no treatment given
- Type of study
- Observational (no treatment given)
- Time in hospital
- Mix of remote tasks and in-person visits
- Drug or intervention
- Not specified by the sponsor
- How long the study runs
- Study runs about 11 months (dates as stated)
- About the drug or intervention
- Not specified by the sponsor
- Patient visit burden
- Not specified by the sponsor
- Type of study
- Observing health over time
- Ages
- 18 Years and over
- Who
- All
- Number of participants
- 40
- Started
- 2026-03-30
- Last checked
- 2026-08
Plain English Summary
What is this study?
- • Testing a new treatment for post intensive care syndrome (pics)
- • Clinical study - 40 participants
- • The primary purpose of this study is to find out whether a wrist-worn activity monitor can help healthcare professionals understand how people recover after they leave the intensive care unit (ICU), where they were cared for when they were most unwell
Who can take part?
- • Ages 18 Years and over
- • Diagnosed with post intensive care syndrome (pics)
Where?
- • Edinburgh - The Royal Infirmary of Edinburgh
- • Edinburgh - Western General Hospital
- • Livingston - St Johns Hospital
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
The primary purpose of this study is to find out whether a wrist-worn activity monitor can help healthcare professionals understand how people recover after they leave the intensive care unit (ICU), where they were cared for when they were most unwell. By tracking recovery at home, the device may help identify problems early so that the right support can be provided. The study involves adults who are discharged from the ICU in three hospitals in Edinburgh. The main questions it aims to answer are: * Can movement data from a wearable device give useful information about how people feel and function after they return home following ICU and then hospital discharge? * Do changes in activity levels relate to changes in symptoms like pain, anxiety or behavioural measures like daily functioning, sleep and cognition? There is no comparison group in this study. Participants will: * Wear a wrist-worn activity monitor * Answer a short set of health-related questionnaires
More detail
Many people who survive a critical illness continue to face physical, emotional, and social challenges for a prolonged period afterwards. The Critical Care Recovery Service (CCRS) supports recovery across three acute hospitals in NHS Lothian, providing coordinated physical and psychological rehabilitation for ICU survivors. Within this diverse group, rehabilitation needs are graded as low or high risk using a validated screening checklist to identify patients with complex health and social care needs. This study is designed to collect patient reported outcome data and movement data from the dominant wrist using an accelerometer among CCRS patients. Adult patients identified as being at high risk of complex rehabilitation needs are subjected for voluntary enrolment at hospital discharge. In addition to the routine CCRS follow ups, participants in our study complete a structured telephone assessment to evaluate their health related quality of life, physical capabilities, and cognitive function over the two months following discharge, complemented by continuous wrist worn accelerometry for the entire study period. This study will provide early evidence on the feasibility and value of integrating continuous wearable monitoring with repeated patient-reported assessments during the early post-ICU period. By linking real-world activity patterns with key domains of recovery, the findings will help identify meaningful digital indicators of deterioration or unmet rehabilitation needs.
How this trial compares with your answers
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What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.
Eligibility at a Glance
Key info
- Age: 18 Years and over
- Who can join: All genders
What the study is looking for
- ✓Adults aged 18 years or older
- ✓Mechanical ventilation for more than 3 days
- ✓Total ICU length of stay greater than 7 days
- ✓Classified as "High Risk" using a validated High-Risk Tool\*
- ✓Expected to be discharged from hospital within the next several days
Who cannot take part
- ✗Primary neurological diagnosis as the reason for ICU admission
- ✗Identified by the clinical team as being on the palliative care pathway
- ✗Physical activity primarily limited by the acute injury (e.g., major trauma or limb amputation)
- ✗Unable to mobilise independently prior to the index hospitalisation requiring ICU admission due to a long-term...
- ✗Lack of capacity or inability to provide agreement to take part
See the full criteria
Where Is This Study? (3 UK sites)
The Royal Infirmary of Edinburgh
Edinburgh EH16 4SA, United Kingdom
Western General Hospital
Edinburgh EH4 2XU, United Kingdom
St Johns Hospital
Livingston EH54 6PP, United Kingdom
How to Get in Touch
Zoeb Jiwaji, Dr
Sponsor contactCONTACT
Barat Ospanov, Dr
Sponsor contactCONTACT