NCT07136298

Brief Summary

The aim of this project is to assess the ability of different groups of National Heath Service (NHS) professionals to correctly identify clinical seizures, and distinguish them from other movements commonly seen in the ICU environment, when shown digital video recordings only. Patients on the ICU are at risk of having seizures, however also commonly make other movements, including shivering, jerking, tics and tremors. An Electroencephalogram (EEG) records the brain wave activity and can help distinguish epileptic seizures from other movements. In a study by Bendadis et al (2010), 52 video-EEGs were reviewed containing "possible seizures" on the ICU. They found only 27% recorded actual epileptic events, with the other 73% having a range of other movements. Malone et al (2009) studied accuracy of diagnosis of 20 video recordings of clinical episodes on the neonatal unit, comparing different staff groups. They found no significant difference between Doctors and Nurses in correctly identifying seizures, however found that accuracy of diagnosis was generally poor. Clinical scientists are currently expanding their roles and responsibilities across Neurophysiology, including giving consultant-level advice on EEG investigations. EEG recordings on the ICU are often obscured by excessive, unavoidable electrical/movement artefacts caused by equipment such ventilators and pumps, and patient factors such as position, breathing artefact and suctioning. These make the EEG difficult to interpret (Boggs 2021). Assessing the clinical signs and symptoms which we may see in ICU patients, in the absence of interpretable EEG, is an essential skill. This study aims to assess Clinical Scientists skills at clinical interpretation, in comparison with other staff groups in the ICU setting. Staff will be asked to watch video clips of events captured in the ICU, and tell us whether they think they are seizures or not, and explain their thought process behind the decision.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Mar 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 3, 2025

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

July 18, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

August 22, 2025

Completed
9 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2025

Completed
Last Updated

August 22, 2025

Status Verified

August 1, 2025

Enrollment Period

6 months

First QC Date

July 18, 2025

Last Update Submit

August 14, 2025

Conditions

Keywords

Intensive CareClinical ScientistNeurologistsIntensivistsITU Nurses

Outcome Measures

Primary Outcomes (1)

  • Level of Agreement

    The primary outcome measure is the level of agreement between the clinical opinion of the different staff groups and the EEG result

    through study completion, an average of 1 year

Secondary Outcomes (2)

  • Interrater Reliability

    through study completion, an average of 1 year

  • Thematic Analysis

    through study completion, an average of 1 year

Study Arms (6)

Clinical Scientists

Other: Clinical Opinion

Advanced Clinical Practitioners

Other: Clinical Opinion

Intensivists

Other: Clinical Opinion

Clinical Neurophysiologists

Other: Clinical Opinion

Neurologists

Other: Clinical Opinion

ICU Nurses

Other: Clinical Opinion

Interventions

Staff participants will be asked to review video clips of events captured during EEGs performed on the ICU and asked to state whether they think the event was an epileptic seizure or not, and what aspects of each event led them to that decision

Advanced Clinical PractitionersClinical NeurophysiologistsClinical ScientistsICU NursesIntensivistsNeurologists

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population are staff working in the Adult ICU at Nottingham University Hospitals, in one of the following groups; Neurophysiology Scientists/Clinical Physiologists, Neurophysiologists, Neurologists, Intensivists, Advanced Clinical Practitioners and Nursing Staff

You may qualify if:

  • Staff working at Nottingham University Hospitals (NUH) in one of the following staff groups;
  • Neurophysiology Scientists/Clinical Physiologists at Band 7 level and above,
  • Neurophysiologists who have completed the CCT in Neurophysiology with at least 1 year of Adult ICU experience.
  • members of the Neurology medical team with at least 1 years' experience of covering ITU
  • Intensivists with at least 1 year's experience working on the Adult intensive care unit
  • Nursing staff working on the Intensive care unit with at least 1 year's experience

You may not qualify if:

  • Staff not employed by NUH i.e. agency staff
  • Staff in other groups not mentioned above

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nottingham University Hospitals

Nottingham, Nottinghamshire, NG7 2UH, United Kingdom

RECRUITING

MeSH Terms

Conditions

Seizures

Condition Hierarchy (Ancestors)

Neurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

James S Baird

CONTACT

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 18, 2025

First Posted

August 22, 2025

Study Start

March 3, 2025

Primary Completion

August 31, 2025

Study Completion

August 31, 2025

Last Updated

August 22, 2025

Record last verified: 2025-08

Locations