NCT07685145Completed
Clinical Decision Support System for Early Mobilization in the Neuro-ICU
Implementation and Feasibility of a Clinical Decision Support System for Early Mobilization in the Intensive Care Unit
Source: ClinicalTrials.gov · Last updated 6 Jul 2026
Brief summary (registry, in English)
This study aims to evaluate the feasibility, safety, and user acceptability of a tablet- and smartphone-based Clinical Decision Support System (CDSS) designed to guide early mobilization for patients with severe neurological conditions in the intensive care unit (ICU). The CDSS standardizes safety screening across neurological, physiological, and device-related domains and provides graded mobility recommendations from Level 0 (passive range of motion) to Level 10 (independent ambulation). The single-center, single-arm feasibility study will be conducted over six months in neurosurgical and trauma ICUs. Adult patients (≥18 years) with traumatic brain injury, intracerebral hemorrhage, subarachnoid hemorrhage, or acute ischemic stroke will be included. Primary outcomes include protocol adherence, data completeness, and user satisfaction (System Usability Scale). Secondary outcomes include time to first mobilization, maximum mobility level achieved, and adverse event incidence.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 25 (actual)
- First submitted
- 21 Jun 2026
- Start date
- 17 Sept 2025
- Primary completion date
- 22 May 2026
- Lead sponsor
- National Taiwan University Hospital
- Diseases
- Stroke
- NCT number
- NCT07685145
What you commit to
- Study type: Interventional
- Participants enrolled: 25
- From 17 Sept 2025 to the primary completion date, 22 May 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Pre-existing severe physical disability (modified Rankin Scale ≥4 before admission).
- Unstable intracranial pressure or craniectomy with active cerebrospinal fluid leakage.
- Unstable fractures or contraindications for mobilization as determined by the attending physician.
- Palliative care status or do-not-resuscitate (DNR) orders.
- Patients unable to participate in mobilization assessment due to medical instability or family refusal.
Who the study is looking for
- Adults (≥18 years) admitted to the neuro-ICU or trauma ICU.
- Diagnosis of acute neurological conditions, including traumatic brain injury (TBI), intracerebral hemorrhage (ICH), subarachnoid hemorrhage (SAH), or acute ischemic stroke (AIS).
- Hemodynamically stable and deemed eligible for rehabilitation evaluation.
- Expected ICU stay ≥48 hours.
Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| National Taiwan University Hospital NTUH Coordinator of this site? Confirm its status | Taipei | Taiwan | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.