NCT06504641

Brief Summary

BACKGROUND: Older patients with frailty have complex support needs. How they manage with daily tasks such as eating and drinking, mobilising, communicating their preferences, and the level of support they need, can vary on a day-to-day basis. They are at risk of rapid loss of functional independence when they are acutely unwell. When older people need input from multiple different professionals, ineffective communication is sadly very common. This leads to disjointed care, and patients becoming frailer and suffering avoidable health complications. One of the problems is that it can be difficult for healthcare professionals to build up a complete picture of a patient from brief verbal handovers and written information in medical records. It is believed that video-recordings capturing the changing functional abilities and support needs of individual patients could improve care-provider communication and support for older people. Smartphones with cameras are now a part of everyday life, and people often tell their stories using photographs and videos. However, video recording patients during care delivery is not commonplace. It is not know how patients and carers feel about being video recorded or whether video recordings improve care. AIM: To explore the perspectives of frail older patients, carers, and clinical staff around video recording during routine clinical care, and to understand how patient videos could impact on communication and care delivery across care transitions. METHODS: The study team will recruit frail, older inpatients, their carers, and clinical staff from a Medicine for the Elderly ward. Over three months, doctors, nurses, and therapists will securely record and view patient videos alongside providing usual care. Videos will capture patients' functional abilities and support needs to inform ongoing assessment and care delivery. The investigators will collect information from patients/ carers/ doctors/ nurses /therapists about their experiences of the video recording intervention through interviews and questionnaires.

Trial Health

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
95

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Feb 2024

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

February 14, 2024

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

July 10, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

July 17, 2024

Completed
14 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2024

Completed
Last Updated

July 18, 2024

Status Verified

July 1, 2024

Enrollment Period

6 months

First QC Date

July 10, 2024

Last Update Submit

July 16, 2024

Conditions

Keywords

FrailtyCommunicationPatient assessmentVideo-recordingCare transitionsCare continuity

Outcome Measures

Primary Outcomes (6)

  • Intervention acceptability [1]

    Patient and carer perspectives on the acceptability of video-based records will be assessed within this mixed-methods feasibility study and process evaluation multiple measures: \[a\] Proportion of eligible participants declining enrolment and reasons for non-participation (% declining, descriptive statistics)

    Within three-month pilot phase

  • Intervention acceptability [2]

    Patient perspectives on the acceptability of video-based records will be assessed within this mixed-methods feasibility study and process evaluation multiple measures: \[b\] Proportion of enrolled patients with ≥ 1 video linked to the electronic patient record (% with at least one video linked to electronic patient record, descriptive statistics)

    Within three-month pilot phase

  • Intervention acceptability [3]

    Patient and carer perspectives on the acceptability of video-based records will be assessed within this mixed-methods feasibility study and process evaluation multiple measures: \[c\] Semi-structured interview at or within 2 weeks of discharge (Framework analysis to understand patient and carer views on acceptability)

    At or within two weeks of patient discharge

  • Intervention acceptability [4]

    Ward team perspectives on the acceptability of video-based records will be assessed within this mixed-methods feasibility study and process evaluation multiple measures: \[a\] Video evaluation questionnaire (a combination of stuctured and open-ended questions asking ward team to appraise whether video quality is suitable for clinical interpretation: Yes/No/To some extent; Video length: Too long/Too short/Just right, Whether ward team want to see more patient videos in the future: Yes/No - descriptive statistics. Open-ended questions ask ward team to explain their answers)

    Within three-month pilot phase

  • Intervention acceptability [5]

    Ward team perspectives on the acceptability of video-based records will be assessed within this mixed-methods feasibility study and process evaluation multiple measures: \[b\] Semi-structured interview after the three-month pilot (Framework analysis to understand ward team views on acceptability)

    Ward staff interviews to be conducted within two months after three-month pilot phase

  • Intervention acceptability [6]

    Ward team perspectives on the acceptability of video-based records will be assessed within this mixed-methods feasibility study and process evaluation multiple measures: \[c\] Number of videos requested, attempted \& submitted (Quantitative, descriptive statistics)

    Within three-month pilot phase

Secondary Outcomes (10)

  • Intervention feasibility - Patient enrolment [1]

    Within three-month pilot phase

  • Intervention feasibility - Patient enrolment [2]

    Within three-month pilot phase

  • Intervention feasibility - Intervention barriers and facilitators [1]

    At or within two weeks of patient discharge

  • Intervention feasibility - Intervention barriers and facilitators [2]

    Ward staff interviews to be conducted within two months after three-month pilot phase

  • Intervention feasibility - Use of the Isla platform [1]

    Within three-month pilot phase

  • +5 more secondary outcomes

Study Arms (3)

Patients

Up to 30 adults, aged 65 years or older, who are frail or pre-frail, and who are admitted as an inpatient to an acute Medicine for the Elderly ward during a three-month pilot phase Intervention: Isla for Frailty - video-based patient records. Isla is a technology company providing a visual patient record platform. The platform allows anyone involved in a patient's care to capture and review visual data (photographs, videos) relating to a patient's health. The platform is web-based (a "progressive web application") and supports secure capture of visual data with encrypted storage in the cloud. Isla interfaces with Electronic Health Record (EHR) systems including Cerner, enabling health professionals to view data held on Isla's servers from within the electronic patient record, via the 'Cerner Red Button'. Health professionals can also view a patient's visual record through a secure weblink requiring an NHS email address and password.

Other: Isla for Frailty

Carers

Carers of enrolled patients, who are in receipt of the Isla for Frailty intervention (described above) Carers are those who provide the enrolled patient with assistance in their daily activities and are unpaid for these caring activities. A carer may be a member of the patient's family, a friend, or other person who provides the patient with unpaid care.

Other: Isla for Frailty

Ward team

Clinical staff working on one of three Medicine for the Elderly wards at St Mary's Hospital, where the Isla for Frailty intervention (described above) will be subject to a feasibility trial. Clinical staff must work regular shifts on the ward during study initiation and pilot phases.

Other: Isla for Frailty

Interventions

Isla for Frailty - video-based patient records. Isla is a technology company providing a visual patient record platform. The platform allows anyone involved in a patient's care to capture and review visual data (photographs, videos) relating to a patient's health. The platform is web-based (a "progressive web application") and supports secure capture of visual data with encrypted storage in the cloud. Isla interfaces with Electronic Health Record (EHR) systems including Cerner, enabling health professionals to view data held on Isla's servers from within the electronic patient record, via the 'Cerner Red Button'. Health professionals can also view a patient's visual record through a secure weblink requiring an NHS email address and password.

CarersPatientsWard team

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients: Adults, aged 65 years or older, who are frail or pre-frail, and who are admitted as an inpatient to an acute Medicine for the Elderly ward during a three-month pilot phase Carers: Carers of enrolled patients, who provide the enrolled patient with assistance in their daily activities and are unpaid for these caring activities. A carer may be a member of the patient's family, a friend, or other person who provides the patient with unpaid care Ward team: Clinical staff working on one of three Medicine for the Elderly wards at St Mary's Hospital, where the Isla for Frailty intervention (described above) will be subject to a feasibility trial

You may qualify if:

  • Admitted as an inpatient to an acute Medicine for the Elderly ward at St Mary's Hospital during a 3-month pilot phase of Isla's visual record platform
  • Aged ≥65 years old
  • Are considered to be frail or pre-frail by the direct care team
  • Have capacity to consent to study participation OR lack capacity to consent on the condition that a 'personal consultee' is available to advise on the patient's likely wishes and feelings about taking part.

You may not qualify if:

  • Patients who lack capacity to consent will be excluded if a personal consultee is not available to advise on the patients' likely wishes or feelings about taking part.
  • Carers.
  • Aged ≥18 years
  • Provide the patient/care-recipient with assistance in their daily activities and are unpaid for these caring activities
  • Are willing to participate in an interview as part of the study
  • A carer may be a member of the patient's family, a friend, or other person who provides the patient with unpaid care
  • \- Carers will be excluded if the patient/care-recipient declined to participate in the study
  • Ward team.
  • Clinical staff working on an acute Medicine for the Elderly ward at St Mary's Hospital.
  • Staff must be working regular shifts on the ward during study initiation and pilot phases
  • Staff must have an active nhs.net account.
  • Ad-hoc bank/agency staff
  • Permanent staff on long-term leave (e.g. sick/maternity) during the pilot

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

St Mary's Hospital

London, W2 1NY, United Kingdom

RECRUITING

MeSH Terms

Conditions

FrailtyCommunication

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and SymptomsBehavior

Study Officials

  • Phoebe Averill, PhD

    Imperial College London

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Phoebe Averill, PhD

CONTACT

Erik Mayer, PhD FRCS

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 10, 2024

First Posted

July 17, 2024

Study Start

February 14, 2024

Primary Completion

July 31, 2024

Study Completion

September 30, 2024

Last Updated

July 18, 2024

Record last verified: 2024-07

Data Sharing

IPD Sharing
Will not share

Locations