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A person-centred model of residential respite care transition support: The Transition Support-Person Centred Care (TS-PCC) Program for family caregivers and care recipients with dementia

A randomised control trial of the use of the Transition Support - Person Centred Program (TS-PCC) compared with usual care, for family caregivers and care recipients with dementia, to improve the experience of residential respite care.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614000043639
Acronym
TS-PCC
Enrollment
20
Registered
2014-01-17
Start date
2013-09-24
Completion date
2014-06-30
Last updated
2020-01-13

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 design to be employed is a cluster randomized controlled trial of a multi-component intervention designed to improve the experience of Residential Respite Care (RRC) for people with dementia and their carers. Clustering will occur at the facility level with randomisation by necessity occurring at this level in order to prevent contamination of results due to changed processes during RRC admission required by the intervention. Thus, two facilities will be allocated as the intervention facilities and two as control facilities. Random allocation will occur via a random number generator. The program will provide support and communication before, during and after residential respite admission in order to facilitate the transition to respite care. Participants with dementia (PWD) and their carers will be interviewed face – to –face and also complete self –report instruments 2 weeks prior to moving into RRC. Allocation of residents will occur to either intervention or control group and all will be assessed during RRC admission. PWD and their carers will be interviewed face to face and asked to complete self report measures when transiting back to home care. PWD and their carers will be interviewed via telephone and asked to complete self report measures three months following return to home care.

Interventions

The TC-PCC Intervention is a structured, person-centred approach aimed at facilitating a positive residential respite care experience for both people with dementia and their carers at each stage of the process of using residential respite care, from the preparation for respite care, through the respite experience and after the return home. Intervention will commence 1-2 weeks prior to admission and continues throughout the length of the respite admission (approximately 1-6 weeks) for a total d

The TC-PCC Intervention is a structured, person-centred approach aimed at facilitating a positive residential respite care experience for both people with dementia and their carers at each stage of the process of using residential respite care, from the preparation for respite care, through the respite experience and after the return home. Intervention will commence 1-2 weeks prior to admission and continues throughout the length of the respite admission (approximately 1-6 weeks) for a total duration ranging from 3-8 weeks depending on length of admission. A core feature of the Intervention is a liaison nurse, who will be the pivotal point of connection between the dyad and Residential Aged Care Facility (RACF) staff. The specific components of the Intervention include: A. Structured Person-Centred Communication (Respite Care Personal Profile; Pre-admission case conference between liaison nurse, care recipient and caregiver; up to daily call/email to care giver from liaison nurse to provide up to date feedback on care recipients status; exit interview from liaison nurse to give hand over to caregiver); and B. Person-Centred preparation for respite experience: prepare simple memory book to aid transition; familiar items bag; and carer comfort review to establish what support the caregiver needs.

Sponsors

Queensland University of Technology
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used) (Subject, Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

Group 1: Intervention group (n=10) - 65 years and older, with a diagnosis of dementia, with a confirmed booking for residential respite Group 2: Control group (n=10) - 65 years and older, with a diagnosis of dementia, with a confirmed booking for residential respite Group 3: Family caregiver intervention group (n=10): care giver of person with dementia, aged over 18 years, directly responsible for the care of participating person with dementia, have known person with dementia for more than 10 years, have 3 contacts per week with person with dementia Group 4: Family caregiver control group (n=10): care giver of person with dementia, aged over 18 years, directly responsible for the care of participating person with dementia, have known person with dementia for more than 10 years, have 3 contacts per week with person with dementia Group 5: Liaison Nurse (n=2): Registered, enrolled or endorsed enrolled nurses working at the intervention facilities, 21 years and older

Exclusion criteria

Carers under the age of 18 years, no diagnosis of dementia, no residential respite booking

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026