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Clinical Trials/ACTRN12624000218594
ACTRN12624000218594
Recruiting
未知

Assessing the impact of the Enhanced Advance care planning and life Review Longitudinal Intervention Community Outreach (EARLI-comm) program on advance care planning engagement

niversity of New South Wales0 sites120 target enrollmentMarch 5, 2024

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
niversity of New South Wales
Enrollment
120
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 5, 2024
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • The inclusion criteria for participants are:
  • 1\. Belonging to one of the three eligible study populations:
  • a) aged 45 years or older and diagnosed with a progressive (life\-limiting) neurological condition (dementia, Parkinson's disease, Huntington's disease, Motor Neurone disease or mitochondrial disease); or
  • b) aged 45 years or older and diagnosed with Human Immunodeficiency Virus (HIV); or
  • c) aged 65 years or older and scoring between 3 and 7 on the Rockwood Clinical Frailty Scale
  • d) to avoid ambiguity, a person with a cancer\-related diagnosis who also meets criteria 1a, 1b or 1c (and does not meet exclusion criteria 5\) will be eligible;
  • 2\. Living in a private residence in Western Australia or New South Wales (own or rented dwelling, including retirement village or other co\-operative housing, but NOT a residential aged care facility);
  • 3\. Able to communicate in English, Italian, or Chinese (Mandarin or Cantonese);
  • 4\. (if self\-referred) Able and agree to visit one of the approved study sites to undertake screening assessment, written informed consent and baseline data collection in person;
  • 5\. Capable of providing informed consent at initial recruitment and answering baseline questions (successfully completing at least 75% of baseline questions.

Exclusion Criteria

  • The exclusion criteria for participants are:
  • 1\. Unable to or refuse to nominate a general practitioner, treating medical specialist or care navigator for liaison with the study team;
  • 2\. The participant's nominated general practitioner, treating medical specialist or care navigator expresses significant concern about participant or research team safety (either for the participant or for the facilitator) which cannot be appropriately managed (e.g. via use of personal protective equipment and physical distancing, or use of video\-conferencing;
  • 3\. A baseline cognitive assessment indicates greater than moderate level of cognitive impairment (Telephone Montreal Cognitive Assessment Score \<8\);
  • 4\. (only for older adults experiencing frailty study population) A baseline assessment on the Clinical Frailty Scale (CFS) indicates a complete absence of frailty (CFS score \<3\) or greater than severe frailty (CFS score \>7\);
  • 5\. It becomes known that the person is expected to die within 'days or weeks' (based on information provided by a care provider, care navigator, treating medical specialist and/or participant's general practitioner during recruitment process \[i.e. between the time of referral and up until the completion of the informed consent process and follow up with care navigator/doctor].

Outcomes

Primary Outcomes

Not specified

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