RecruitingNot Applicable

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

Denmark198 participantsStarted 2025-08-25

Plain-language 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.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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.

What they're measuring

Amount of physical mobilisation

Timeframe: From admission at the intensive care unit (ICU) until discharge from the ICU, with a maximum of 3 months.

Amount of high-level mobilisation

Timeframe: From admission at the intensive care unit (ICU) until discharge from the ICU, with a maximum of 3 months.

Association between intensity and duration of mobilisation

Timeframe: From admission at the intensive care unit (ICU) until discharge from the ICU, with a maximum of 3 months.

Trial details

NCT IDNCT07548580

SponsorRigshospitalet, Denmark

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2026-06

Contact for this trial

Christian Gunge Riberholt, PhD

0045-38631600 christian.gunge.riberholt@regionh.dk

View on ClinicalTrials.gov More Acute Brain Injury trials

Plain-language summary

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Amount of physical mobilisation

Timeframe: From admission at the intensive care unit (ICU) until discharge from the ICU, with a maximum of 3 months.

Amount of high-level mobilisation

Timeframe: From admission at the intensive care unit (ICU) until discharge from the ICU, with a maximum of 3 months.

Association between intensity and duration of mobilisation

Timeframe: From admission at the intensive care unit (ICU) until discharge from the ICU, with a maximum of 3 months.