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Video-recOrded hospItal dischaRge (VOIR)

Evaluating Feasibility and Acceptability of Video Discharge Hosted in Patient Knows Best or Ortus-iHealth Apps: A Feasibility Randomised Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06512272
Acronym
VOIR
Enrollment
60
Registered
2024-07-22
Start date
2024-08-01
Completion date
2024-10-31
Last updated
2024-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ALL, Adult

Keywords

hospital discharge, video recorded discharge, transition of care, mobile application

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 or standard care supplemented with video-recorded discharge. Clinical teams record briefings covering medication and wound care, which patients can access multiple times on their smart devices. Patients and clinical staff complete questionnaires to assess acceptance and feasibility. Feasibility is determined by recruitment, retention, and completion rates, with patient engagement and viewing habits also analyzed. The study aims to enhance patient understanding and continuity of care through accessible discharge information.

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 design, with one group receiving standard discharge care and another receiving the standard care plus video-recorded discharge. Upon discharge from hospital, the clinical team (e.g, nurses and doctors) will record the routine discharge briefing, covering aspects such as medication and wound care, for consenting patients. This briefing will be based on the discharge letter from the medical team and will last approximately up to three minutes. It will take place in a private hospital ward room, using the patient's or their relative's smart device (e.g., mobile or tablet). Subsequently, the recorded video will be uploaded to the patient's Patient Knows Best app account. Patients can review the video multiple times to reinforce their understanding of the discharge information, including medication advice, wound dressing, and exercise. Additionally, they can share it with their relatives, as well as community and district nursing teams, to enhance the clarity of shared information and continuity of care. Both control and intervention group patients will receive a self-reported questionnaire regarding their acceptance of the discharge process, satisfaction levels, and its impact on their quality of life. Clinical staff involved in the recording will also complete a questionnaire assessing the feasibility, practicality, and satisfaction with the new intervention. The feasibility of the study will be evaluated based on recruitment numbers, retention rates, completion rates, and the chosen questionnaire's suitability. Questionnaires will be administered post-discharge, one week after discharge, and thirty days later. Additionally, patient engagement with the Patient Knows Best platform and video viewing habits will be analysed to explore any differences among demographic groups.

Interventions

OTHERVideo recorded shared using a mobile application

The routine hospital discharge explanation is video recorded \[up to three minutes\]. The video is uploaded by to a mobile app for the patient and patient/ relatives can review the advice multiple times

Sponsors

Basildon and Thurrock Hospitals NHS FoundationTrust
CollaboratorUNKNOWN
Southend NHS Foundation Trust
CollaboratorOTHER
Anglia Ruskin University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Randomisation on a ratio of 1:1 * A: allocated usual care * B: allocated intervention group which include usual care plus video-recorded discharge

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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 criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Acceptability of video-discharge7 days and 30 days post-dischargeQuestionnaire with close ended and open ended question based on validated questionnaire

Secondary

MeasureTime frameDescription
Patient satisfaction7 and 30 days post dischargeBrief questionnaire on patient satisfaction
Care of Transitions7 and 30 days post dischargeThree questions measuring validated tool
Staff satisfaction of video recorded dischargewithin 7 days of post-discharge experienceClose and opened questionnaire

Contacts

Primary ContactNaim Abdulmohdi, PhD
naim.abdulmohdi@aru.ac.uk(+44)1223695538

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026