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N/A N=83 Supportive Care

The Hospice Advanced Dementia Symptom Management and Quality of Life Trial

Dementia

Enrolled (actual)
83
Serious AEs
45.5%
Results posted
Jul 2020
Primary outcome: Primary: Percentage of Hospice IDT Members Who Complete Required Education and Training — 92 percentage of participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Dementia symptom management at home hospice edition (Behavioral); Education and Training (Behavioral)
Age
Adult, Older Adult · 50+ yrs
Sex
All
Sponsor
NYU Langone Health
Primary completion
Jun 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Hospice IDT Members Who Complete Required Education and Training
92

Summary

Alzheimer's Disease and Related Disorders (dementia) are a group of serious life limiting illness that cause significant challenges to our public health system, with significant illness burden for both the person with dementia and the caregiver. At the end of life, over 230,000 persons with dementia annually are cared for in hospice, yet hospice agencies are ill prepared to care for this population and often resort to inappropriate pharmacologic measures such as antipsychotics that reduce quality of life rather than improve it. This study will therefore through its two phases refine and then implement, using a pragmatic stepped wedge trial design, the Dementia Symptom Management at Home Program Hospice Edition, with the goal improving quality of care for the person with dementia and their caregiver, reducing antipsychotic use, and increasing bereaved caregiver satisfaction in the hospice setting.

Eligibility Criteria

Inclusion Criteria

  • Must have dementia as primary diagnosis for admission to hospice
  • Must be newly admitted to a participating hospice
  • Must be 50 years or older

Clinicians:

  • Must be a skilled clinician or home health aide who provides care through an eligible home health agency
  • Must be 18 years or older

Exclusion Criteria

Persons with Dementia:

  • None

Clinicians:

  • None
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03681119). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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