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Optimising support for Chinese carers of people with dementia by embedding iSupport in routine care services

Optimising support for Chinese carers of people with dementia by embedding iSupport in routine care services

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12623000323628
Enrollment
260
Registered
2023-03-27
Start date
2023-05-22
Completion date
2025-01-30
Last updated
2025-09-22

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

Conditions

None listed

Brief summary

The research project aims to (1) to determine the effectiveness of the ‘Tailored iSupport’ intervention for carers and people with dementia; and (2) to evaluate the effectiveness of the implementation strategies applied to embed the ‘Usual support’ and the ‘Tailored iSupport’ into the routine services of aged care organisations in real-world settings. The study will also explore the experiences of carers, frontline staff and facilitators in the project. The hypotheses tested in the study are described in the following: 1. Carers receiving the ‘Tailored iSupport’ will report 1) a higher level of QoL; 2) a higher level of Self-Efficacy; 3) a significantly higher level of QoL for the person they care for via a proxy rating; 4) fewer unplanned hospital admissions, less emergency department use and a lower level of permanent admission into residential aged care by the person they care for; 5) better quality care experiences of persons with dementia via proxy ratings, compared to those in the ‘Usual iSupport group’.

Interventions

This is a type 2 hybrid effectiveness-implementation randomised controlled trial to (1) determine the effectiveness of the ‘Tailored iSupport’ intervention for carers and people with dementia and (2) to evaluate the effectiveness of the implementation strategies applied to embed the ‘Tailored iSupport’ into the routine services of aged care organisations in real-world settings. The study will also explore the experiences of carers, frontline staff and facilitators in the project. The interventio

This is a type 2 hybrid effectiveness-implementation randomised controlled trial to (1) determine the effectiveness of the ‘Tailored iSupport’ intervention for carers and people with dementia and (2) to evaluate the effectiveness of the implementation strategies applied to embed the ‘Tailored iSupport’ into the routine services of aged care organisations in real-world settings. The study will also explore the experiences of carers, frontline staff and facilitators in the project. The interventions in the study are outlined in the following: Carers in the ‘Tailored iSupport’ group will be assigned to a trained facilitator, who is a health professional or social care professional with expertise in dementia care. The facilitators will undergo 3 x 2 hours online workshops over a 2-week period and the training sessions will be provided 6 weeks prior to initiation of the intervention. The training sessions will be relative to delivering the intervention including: 1) Introduction to the project; 2) being an effective facilitator and 3) recruitment, data collection and outcome measures used in the project. The CIs in the project will provide the training sessions. Moreover, facilitators will participate in a 30-minute online debrief and coaching session every 2 weeks with the CIs in the project during the intervention period to ensure their facilitation alights with the intended project outcomes and to help them with problem-solving skill development. The facilitators will provide individualised support to carers by engaging them in: 1) relevant iSupport modules: The facilitator will assess carers’ individualised needs in the program in an individual meeting lasting 45-60 minutes 2 weeks prior to the intervention using the ‘Risk Appraisal Measure’ (Adapted from Czaja et al. 2009). The facilitator will recommend learning modules, for example ‘Module 5 Dealing with changed behaviours’ when the carer reports sudden/worrisome changes in care recipient’s memory and mood. 2) monthly peer support group meetings lasting about 30-45 minutes (online or face-to-face): The meeting will include up to 8 carers. 3) weekly text messages extracted from iSupport to target carers’ learning needs; 4) resources/services tailored to their needs: Carers are encouraged to make individual appointments with their facilitator to request assistance to access and utilise resources/services when their care recipients experience changes, for example in the case of sudden changes in behaviours, the facilitator will recommend GP visit to identify the causes or refer them to Dementia Support Australia (in Australia’s study sites only). Facilitators will maintain a portfolio to record all contact instances with carers throughout the intervention period. 5) The facilitators will provide monthly staff training on iSupport during the intervention period using the existing paid staff development time, provide practical support for frontline staff in the workplace regarding partnership with carers. The intervention will last 6 months.

Sponsors

Australian Nursing Home Foundation
Lead SponsorCommercial sector/Industry

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

This study will be undertaken in aged care organisations in Australia and Community Health Centres (CHCs; primary care managed by general practitioners and registered nurses) in China. In Australia, participants will be recruited in community aged care settings managed by three Chinese ethno-specific aged care organisations based in Adelaide (South Australia) and Sydney (New South Wales). In China, participants will be recruited in 6 CHCs in Xian’s Shanxi Province and in Zunyi, Guizhou Province respectively. There are three participant categories, namely Chinese carers of people with dementia (PWD), frontline staff and iSupport facilitators, in the study. Inclusion criteria for Chinese carers of people with dementia (PWD): aged 18 years or over; caring at least twice a week for an adult living with dementia. If a care recipient has no formal dementia diagnosis but meets cognitive impairment using the "AD8 Dementia Screening Interview" (Li et al. 2012). Exclusion criteria: carers have severe mental health conditions or terminal illness themselves; are involved in other studies or participated in the previous iSupport RCT trial. Inclusion criteria for frontline staff: frontline staff involved in the care of PWD and the carers to the study will be invited to participate. Inclusion criteria for iSupport facilitators: The iSupport facilitators will be appointed by their organisations through an internal selection process. They will be health care professionals or social care professionals with at least 2 years experiences in the care of people with dementia.

Exclusion criteria

Exclusion criteria for Chinese carers of people with dementia (PWD): (1) carers have severe mental health conditions or a terminal illness; (2) carers involve in other studies. Exclusion criteria for Chinese carers of frontline staff: agency staff.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026