MedPath

Extension Connection Evaluation

Completed
Conditions
Dementia
Interventions
Behavioral: Educational activities to improve dementia care
Registration Number
NCT02455310
Lead Sponsor
Ryan M. Carnahan
Brief Summary

This study will perform a retrospective analysis to evaluate the effectiveness of a multicomponent educational intervention to improve medication use and management of behavioral and psychological symptoms of dementia, relative to a statewide intervention that has been ongoing. Medication use and symptom severity outcomes will be compared among intervention counties and demographically similar non-intervention counties.

Detailed Description

This study will perform a retrospective analysis to evaluate the effectiveness of a multicomponent educational intervention to improve medication use and management of behavioral and psychological symptoms of dementia, relative to a statewide intervention that has been ongoing. Medication use and symptom severity outcomes will be compared among 29 intervention counties and 10 demographically similar non-intervention counties. The long-term effectiveness of the statewide intervention will also be evaluated. Medicare and Minimum Data set data from 2011 to 2014 will be used to evaluate prescribing and other outcomes in 1) outpatients with dementia, and 2) nursing home residents, based on exposure to interventions among healthcare and nursing home providers. Measurable goals included increasing the appropriateness of antipsychotic prescribing and reducing anticholinergic use. Effect modification will be evaluated by level of participation in the intervention and other prescriber and nursing home facility characteristics.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
44524
Inclusion Criteria
  1. Current Medicare fee-for-service plan and Part D enrollment for at least 3 months prior to the month of interest and during the month of interest (allowing a gap of one month to be considered as continuous enrollment if the person is enrolled during the month of interest)
  2. Age greater than or equal to 66 years at the end of a year of interest
  3. Any dementia diagnosis prior to the month of interest, or current resident of a nursing home
  4. For the nursing home analysis, at least 14 days in the facility in the month being classified
Exclusion Criteria
  1. Greater than 15 days of the month of interest when prescription fills are unobservable from Medicare Part D claims due to hospital inpatient status, skilled nursing facility resident status, or hospice enrollment
  2. A diagnosis of schizophrenia, schizoaffective disorder, bipolar disorder, Huntington's disease, Down's syndrome, or mental retardation or developmental disability at any time during the study period. Diagnoses after entry into the study sample will be included because of the limited look-back period to define some conditions for some individuals, and because these are generally not conditions with late-life onset so they are assumed to have been present prior to the first occurrence of a diagnosis in the available data
  3. Currently comatose based on the most recent MDS assessment-if currently in a nursing home

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Outpatients with dementiaEducational activities to improve dementia careMedication use will be evaluated among outpatients with dementia in intervention and control counties, as well as statewide to evaluate the long-term effectiveness of the statewide intervention.
Nursing home residentsEducational activities to improve dementia careMedication use and behavioral outcomes will be evaluated among nursing home residents in intervention and control counties, as well as statewide to evaluate the long-term effectiveness of the statewide intervention.
Primary Outcome Measures
NameTimeMethod
Anticholinergic UseUp to 4 years

Anticholinergic use

Antipsychotic useUp to 4 years

Antipsychotic use

Secondary Outcome Measures
NameTimeMethod
Olanzapine use in patients with metabolic disordersUp to 4 years

Proportion of antipsychotic users with diabetes mellitus, hyperlipidemia, or hypertension (based on diagnosis indicators from claims) who receive olanzapine, the least appropriate antipsychotic when these conditions are present due to its metabolic effects.

Excessive antipsychotic doseUp to 4 years

Antipsychotic doses as defined as excessive by CMS standards for nursing home residents with dementia

Quetiapine or clozapine use only among antipsychotic users with Parkinson's disease or Lewy body dementiaUp to 4 years

Quetiapine or clozapine use only among antipsychotic users with Parkinson's disease or Lewy body dementia. These are the most appropriate antipsychotics in these conditions.

Antipsychotic use in people with dementiaUp to 4 years

Antipsychotic use in people with dementia. This is a subgroup analysis of the nursing home population.

Antipsychotic use in nursing home residents with a potentially appropriate indicationUp to 4 years

Proportion of antipsychotic users with evidence of a potentially appropriate indication, stratified by indication, as follows: verbal or physical aggression, delusions, hallucinations, delirium

Hypnotic useUp to 4 years

Hypnotic use as measured by MDS indicator

Benzodiazepine useUp to 2 years

Benzodiazepine use. Time frame differs because Medicare Part D did not pay for these drugs until 2013.

Antipsychotic use in nursing home residents without a potentially appropriate indication, and proportion with evidence of an inappropriate indicationUp to 4 years

Antipsychotic use in those without a potentially appropriate indication, and proportion of those users with evidence of an inappropriate indication

Antipsychotic use in nursing home residents with a recent history of fallsUp to 4 years

Antipsychotic use in those with a recent history of falls (fall indicator on any MDS assessment in the prior 6 months)

Antipsychotic use in nursing home residents with an unsteady gaitUp to 4 years

Antipsychotic use in nursing home residents with an unsteady gait, as evaluated by MDS records

Changes in behavioral and psychological symptom presenceUp to 4 years

Changes in behavioral symptom frequency (each of verbal aggression, physical aggression, delirium, hallucinations, delusions)

Trial Locations

Locations (1)

The University of Iowa College of Public Health

🇺🇸

Iowa City, Iowa, United States

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