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Digital health solution to enable healthcare consumers to identify and communicate their needs and preferences with healthcare staff.

Feasibility of the MyNeeds digital health solution to enable consumers to identify and communicate their needs and preferences with healthcare staff across a health service care continuum.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12623001041640
Enrollment
106
Registered
2023-09-26
Start date
2023-09-27
Completion date
2024-03-14
Last updated
2024-09-09

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

Conditions

None listed

Brief summary

Models of health care have traditionally been episodic and diagnosis centred. In an era of increased chronic illness, multi-morbidity and disability, there is a clear need for health care to transition towards integrated, person-centred and goal-oriented care. However, aligning care planning and delivery with healthcare consumers’ needs and preferences is operationally challenging, particularly across settings and clinical specialties. The aim of this study is to assess the feasibility of (i) healthcare consumers using a recently codesigned consumer digital health intervention, the MyNeeds intervention, to capture needs and preferences directly from healthcare consumers, and (ii) healthcare staff accessing and using this consumer data to inform person-centred care planning. This study is a non-randomised feasibility study that will be conducted sequentially across two inpatient wards: an acute medical ward; and an inpatient general subacute ward at an Australian metropolitan public health network. Primary outcome will be feasibility assessed using Bowen’s framework across the following focus areas: acceptability; demand; practicality; implementation; adaption; and integration. All consumers admitted to wards one and two during a six-week feasibility testing period will be screened for eligibility and all eligible consumers invited to participate. Consumers will be eligible unless they are: admitted and discharged after hours or on weekends; predicted to be discharged within 24 hours of admission; or currently participating in another unrelated trial where the fidelity of either trial could be impacted. All clinical and clinical support staff working on the test wards during the feasibility testing period will be eligible and invited to participate.

Interventions

Name of intervention: MyNeeds digital health intervention. This digital health intervention was co-designed with healthcare consumers and health service staff using an Experience Based Co-design (EBCD) process. The EBCD process involved a number of steps over a 12-month period, including: 16 focus groups conducted at the program level with a total of 92 staff representing medical, nursing, allied health, pharmacy and support staff; individual in-depth interviews with 12 healthcare consumers; es

Name of intervention: MyNeeds digital health intervention. This digital health intervention was co-designed with healthcare consumers and health service staff using an Experience Based Co-design (EBCD) process. The EBCD process involved a number of steps over a 12-month period, including: 16 focus groups conducted at the program level with a total of 92 staff representing medical, nursing, allied health, pharmacy and support staff; individual in-depth interviews with 12 healthcare consumers; establishment of staff priority areas for the codesign workshops; establishment of consumer priority areas for the codesign workshops; three 120-minute face to face and two virtual codesign workshops with 12 staff members and 7 consumers where the intervention was codesigned (inclusive of content and workflows); and two digital codesign workshops with 7 consumers to refine the layout and design of the MyNeeds intervention. Consumes had the opportunity to interact with the MyNeeds intervention in these digital codesign workshops through their own SMART devices and provide feedback that was used to refine the intervention in preparation for this feasibility study. There are two key processes involved with the MyNeeds digital health intervention: 1) the electronic capture of broad needs and preferences directly from healthcare consumers or their support people; and 2) the integration of these needs and preferences data captured within the MyNeeds Intervention with the health service electronic health record at the patient level. Health service clinicians are able to view consumer needs and preferences in the electronic health record prior to, and during clinical encounters. Health service clinicians are then able to use this information to inform individualised care planning in partnership with the consumer, and if applicable their support people. Materials used: Electronic smart device (such as smart phone or tablet) or computer connected to the internet (either wireless or hard-wired internet). Arden Street Labs Virtual Care Solution, known as Monitor++, that houses the electronic consumer needs and preferences intervention. This virtual care solution is already imbedded into systems at the healthcare organisation where feasibility testing will occur. The electronic health record in use at the health network where feasibility testing will occur. Daily reports from Monitor++ will capture all occasions that a consumer initially populates the MyNeeds intervention, and every occasion that needs and preferences are updated. These reports will be monitored by project staff. Who will deliver the intervention: Healthcare consumers and/or their support people populate the electronic consumer facing survey and view and/or edit the consumer needs and preferences summary page with or without assistance (if required). Populating the MyNeeds consumer facing survey takes approximately 10 t0 15 minutes. Automated electronic process to integrate the consumer needs and preferences data with the electronic health record. Mode of delivery: Consumers use their own smart device (if available), or a hospital supplied device (if the consumer doesn’t have access to their own smart device). Health service clinicians access the consumer needs and preferences data through existing processes to access the electronic health record. Location: The intervention can be accessed by consumers from any location where a smart device is connected to the internet including: emergency departments; hospital wards; community health settings; outpatient clinics; private residences; and residential aged care facilities. Health service clinicians access data collected in the intervention within the healthcare setting that they routinely access health service electronic health records. Timing and dose: The initial consumer needs and preferences survey is populated once. Consumers can then log in and view, and/or update their preferences as often as they choose. There is no requirement for a consumer to update their needs and preferences, nor is there a limit on the number of times that they can update these preferences. Health service staff will have access the consumer needs and preferences data as often as they are logged into the health services electronic health record and have the consumers individual electronic health record open. This feasibility study will run for a total period of 6 months, including two-six week testing periods across an acute medical and an inpatient rehabilitation unit. Procedures and personalisation: Consumers receiving healthcare will be informed of the intervention and invited to register for the intervention. Consumers will have the option to receive assistance with registration and populating the MyNeeds intervention from a support person, a member of the project team, or from a ward-based consumer volunteer. The medical decision maker or next of kin will be approached in cases where the consumer is too unwell to populate the MyNeeds intervention independently or with support. In such cases the medical decision maker or next of kin will populate the MyNeeds intervention as a proxy for the consumer. Consumers will be able to tailor the information that they enter, and the frequency that they update the information in the MyNeeds intervention.

Sponsors

Peninsula Health
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Consumer participants: All consumers admitted to the participating wards during the testing period who are: expected to be an inpatient on the test unit for >24 hours; inpatient admission on the test unit includes stay during Monday to Friday; able to communicate in simple English; and not participating in another unrelated trial. Staff participants: All clinical staff working on the participating wards during the study period and who have access to clinical systems as part of their usual role will be eligible to participate in this feasibility study. Clinical staff will include any medical, nursing, pharmacy, and allied health professional, and assistants (nursing, pharmacy, or allied health assistants) working on the test wards during the study period. Volunteer Participants: Volunteer participants will include all Peninsula Health volunteers who volunteer their time to assisting healthcare consumer participants with the MyNeeds intervention on the participating wards during the feasibility study.

Exclusion criteria

Consumer participants: Consumers will not be invited to participate if they: don't meet the inclusion criteria; are admitted and discharged to the ward on the weekend; expected to be admitted to the ward for <24 hours; currently participating in another unrelated trial; or are unable to communicate in simple English. Staff participants: Staff who do not have access to the electronic health record as part of their usual role working on the test ward. Volunteer Participants: Volunteers not affiliated with Peninsula Health will not be eligible for inclusion.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026