None listed
Conditions
Interventions
Care coordination to improve management of elderly veterans. The intervention will be trialled for 12 months. The control group will receive usual care.
Sponsors
DVA
Study design
Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)
Eligibility
Sex/Gender
All
Age
65 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Prescribed at least five PBS-approved medications; chronic disease.
Exclusion criteria
Not end-stage palliative care.
Outcome results
None listed