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Clinical Trials/NCT06030323
NCT06030323RecruitingNot Applicable

Validation and Testing of Artificial Intelligence Models to Measure Physical Activity in Patients Admitted to Hospital Following a Stroke

Cambridge University Hospitals NHS Foundation Trust1 site in 1 country34 target enrollmentStarted: June 24, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
34
Locations
1
Primary Endpoint
Sensitivity and specificity of AI models

Study Overview

Brief Summary

The research team are developing algorithms using artificial intelligence that use information collected by accelerometers to detect a person's position, such as whether an individual is lying, sitting, or standing, and the individual's movements, such as whether they are taking steps or standing up.

Sensor location will affect the accuracy of the model and acceptability of the method. The research team are therefore developing algorithms for four different locations.

The purpose of the research is for the development of the algorithms and check whether they accurately recognise different positions and movements in people whose movement is affected by a stroke, and by being in a hospital environment (e.g. using a profiling bed).

The research team plan to recruit between 34 and 50 participants who are admitted hospital due to having a stroke. After providing informed consent, participants will be asked to complete a one-off assessment with a member of the research team and a ward physiotherapist. Participants will be asked to wear the four sensors, and move through a series of postures, walk for up to six minutes, and stand as many times as they feel able in one minute.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • admitted to hospital with a diagnosis of an acute stroke.

Exclusion Criteria

  • unable to provide informed consent;
  • receiving end-of-life care;
  • the consultant in charge of their care disagrees with their inclusion

Outcomes

Primary Outcomes

Sensitivity and specificity of AI models

Time Frame: Collected during hospitalisation (up to 12 weeks)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Peter Hartley

Principal Investigator

Cambridge University Hospitals NHS Foundation Trust

Study Sites (1)

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