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Mobility and Activity Patterns in Hospitalised Severe Brain Injury (MAP-ABI)

C

Christian Riberholt

Status

Active, not recruiting

Conditions

Brain Injuries

Treatments

Other: Activity monitor group

Study type

Observational

Funder types

Other

Identifiers

NCT05571462
H-22031667

Details and patient eligibility

About

The purpose of this observational study is to quantify physical activity patterns in patients with severe acquired brain injury admitted for in-hospital rehabilitation.

Full description

Patients admitted for rehabilitation will be included for two periods of one-week monitorization of physical activity. The investigators will include all patients with moderate to severe brain injury.

This is an observational cross-sectional study including patients 18 years or above. Patients with conditions such as unstable fractures that restricts mobilisation are excluded. Physical activity is measured continuously during rehabilitation at two separate seven-day periods using a body-worn activity tracker. The first period will be initiated in the early phase of rehabilitation (3 days after admission) and the second at the late phase (10 days before discharge).

Baseline variables considered predictors, confounders or modifiers for physical activity will be collected along with registration of variables during the measurement periods and functional outcome variables at discharge.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years old

Exclusion criteria

  • Planned discharge within two weeks
  • Fractures of lower extremities, pelvis or spine prohibiting weight-bearing
  • Amputation of lower extremities

Trial design

100 participants in 1 patient group

Activity monitor group
Description:
No intervention will be applied. All patients will have activity monitors placed at the distal part of the femur and on the torso. Normal rehabilitation will be performed as usual.
Treatment:
Other: Activity monitor group

Trial contacts and locations

1

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Central trial contact

Christian Riberholt, PhD; Vibeke Wagner, MsC

Data sourced from clinicaltrials.gov

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