Status:
NOT_YET_RECRUITING
Video-recOrded hospItal dischaRge (VOIR)
Lead Sponsor:
Anglia Ruskin University
Collaborating Sponsors:
Basildon and Thurrock Hospitals NHS FoundationTrust
Southend NHS Foundation Trust
Conditions:
ALL, Adult
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This study evaluates the suitability and acceptability of video-recorded discharge via the Patient Knows Best app. Through a randomized control trial, patients receive either standard discharge care o...
Detailed Description
Study Design The study aims to assess how suitable and acceptable the use of video-recorded discharge via the Patient Knows Best or Ortus-iHealth application is. It employs a randomised control trial...
Eligibility Criteria
Inclusion
- Age \>18 years old
- Anticipated to be discharged to their own home or that of a relative;
- Staying for at least one night on a participating hospital ward;
- Recently discharge (in the last 2 months) from the participating hospital ward with the same clinical problem as assessed by the care professionals;
- From cardiothoracic centre-Basildon or Elderly ward-Southend
- Have a personal digital device (e.g., mobile or tablet)/ or their close relative and mobile app
- Able to read and understand English.
- Relative or patient willing and able to give informed consent
- Clinical Frailty scale of ≤ 8 using Rockwood Frailty Scale
Exclusion
- Patients live out of the area or plan to be transferred to another acute hospital;
- Discharged after recurrent admissions for the same clinical complaint as assessed by the care professionals;
- Patient or immediate carer don't have a personal digital device capable of hosting Patient Knows Best/ Ortus-iHealth app;
- Patient or relative unable or unwilling to upload the personalised discharge video to mobile app;
- Admitted for psychiatric reasons (other than dementia/delirium);
- Identified as being at the end of life and whose care has become palliative / clinical Frailty scale of \> 8 using Rockwood Frailty Scale
Key Trial Info
Start Date :
August 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
October 31 2024
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT06512272
Start Date
August 1 2024
End Date
October 31 2024
Last Update
July 22 2024
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