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Clinical Trials/NCT03864965
NCT03864965CompletedNot Applicable

Responses to a Standardized Approach to Advance Care Planning in Cognitive Disorders Clinic

University of Florida2 sites in 1 country38 target enrollmentStarted: July 1, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
38
Locations
2
Primary Endpoint
Change in rate of advance directive completion during or following the visit

Study Overview

Brief Summary

Advance care planning among patients with cognitive disorders poses unique challenges to clinicians. To improve planning in patients with Alzheimer's disease and other dementias, the researchers suggest a routine, standardized approach to these conversations. The main outcome measure is the rate of entry of Advance Directive completion in the patient's Electronic Health Record (EHR). A control group of similar patients from another provider specializing in cognitive disorders will be used to tease out confounding variable effects.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to 100 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients having mild cognitive impairment (MCI) or very mild to mild dementia (CDR 0.5-1).

Exclusion Criteria

  • •Patients with moderate to severe dementia (CDR 2-3).

Arms & Interventions

Intervention Group

Experimental

Patients diagnosed with mild cognitive impairment, very mild dementia, or mild dementia, will receive the guided advance care planning conversations with the PI

Intervention: Advance Care Planning (Other)

Control Patients

No Intervention

Patients diagnosed with mild cognitive impairment, very mild dementia, or mild dementia, will not receive the guided advance care planning conversations with the PI

Outcomes

Primary Outcomes

Change in rate of advance directive completion during or following the visit

Time Frame: Baseline; Month 6; Month 12; Month 18

Change in the rate of completed advance directives that are uploaded to the patient's electronic medical record

Time Frame: Baseline; Month 6; Month 12; Month 18

Secondary Outcomes

  • Change in Hospital Anxiety and Depression Scale (HADS)(Baseline; Month 2; Month 3)
  • Change in Beck Hopelessness Scale (BHS)(Baseline; Month 2; Month 3)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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