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Recruiting Observational

Physical Mobilisation to Acquired Brain Injury Patients in Intensive Care Units: a Prospective Cohort Study

NCT07548580 · tracked via the Priya Life Science Denmark tracker
Phase
Observational
Started
2025-08-25
Last updated
2026-04-23

Condition(s) studied

Acute Brain Injury

Study summary

The objective of this study is to quantify the amount of physical mobilisation provided to patients with moderate to severe acquired brain injury in Scandinavian neuro-ICs, and the association between intensity and duration of mobilisation, physiological data perceived to be related to the safety of high-level mobilisation, and amount of high-level mobilisation during the neuro-ICU stay.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults (age ≥ 18 years) * Admitted to a neuro-ICU or to a regular ICU with dedicated beds for severe acquired brain injury patients in Scandinavia * Patients with moderate to severe traumatic brain injury (TBI) or stroke * Patients must be intubated and expected to require mechanically ventilation for at least 24 hours. Exclusion Criteria: * Patients that are not likely to survive or for whom a decision has been made on palliative care. * Patients allergic to the Sens monitor patch or showing any type of allergic reactions from the patch after inclusion in the study that needs treatments or results in immediately removal of the patch.

Primary outcome measure(s)

  • Amount of physical mobilisation — From admission at the intensive care unit (ICU) until discharge from the ICU, with a maximum of 3 months.
    Amount of physical mobilisation provided during stay at neuro-ICU
  • Amount of high-level mobilisation — From admission at the intensive care unit (ICU) until discharge from the ICU, with a maximum of 3 months.
    Amount of high-level mobilisation during stay at neuro-ICU
  • Association between intensity and duration of mobilisation — From admission at the intensive care unit (ICU) until discharge from the ICU, with a maximum of 3 months.
    The association between the intensity and duration of mobilisation during stay at neuro-ICU

Trial sites (2)

FacilityCityRegionStatus
Rigshospitalet Copenhagen Denmark Recruiting
Odense Universitets Hospital Odense Denmark Active Not Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07548580 on ClinicalTrials.gov ↗ ← All trials in Denmark