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Would Artificial Intelligence Reduce Delays to Nurse Response Times (WAiRD)

T

The Leeds Teaching Hospitals NHS Trust

Status

Enrolling

Conditions

Nurse's Role

Treatments

Device: novel nurse call system

Study type

Observational

Funder types

Other

Identifiers

NCT06043986
CD22/153868

Details and patient eligibility

About

Patients are admitted to wards at all times of day and night and in various states of ill health. As this research is non interventional and does not impact on patient safety, the guidance from the ethics committee was reviewed and agreed that it would be appropriate to enrol every admission into the 2 bed bays and gain consent within 24 hours of admission.All data collected within the trial using the smart tablets will be associated to a study number, no patient details will be stored on the smart tablet and therefore the cloud data store.It has been discussed with the trust information governance and this complies with their regulations.

Any patient identifiable data will be kept by the research team. All data will be archived and stored as per the Sponsors policy. The novel nurse call system has been designed to be user friendly to all patients regardless of age, learning ability and first language used. By using colours, images and words in the hope that this will be accessible to all. The nursing staff on the ward advised on the main reasons for the nurse call system activation and therefore the icons used in the novel system were adapted from this. This trial was discussed in the patient and public involvement group. As this is a pilot trial, any adaptions that need to be made will be made before the large scale trial.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

All adults 18 years who are admitted to the cardiology admissions ward will be eligible to take part.

Exclusion Criteria: Any patient who does not wish to participate will have their anonymised data removed from the trial.

Trial design

40 participants in 2 patient groups

Bed bay A
Description:
Time from nurse call system activated by the novel nurse call system to initial response time T1 and time to complete task T2. Reason for nurse call system activated: Toilet/Pain/Medication/ /Need a nurse/Other
Treatment:
Device: novel nurse call system
Bed bay B
Description:
Time from nurse call system activated by standard system to initial response timeT1 and time to complete task T2.

Trial contacts and locations

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Central trial contact

Sarah Hall; Lucy Leese

Data sourced from clinicaltrials.gov

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