STOP-FALLS-DDeprescribing to Reduce Injurious Falls Among Older Adults With Dementia
STOP Falls D Educational Intervention
Mental Disorders+3
+ Brain Diseases
+ Central Nervous System Diseases
Services Research Study
Summary
Study start date: February 22, 2023
Actual date on which the first participant was enrolled.The study design is a pragmatic, one-arm pilot trial to test the feasibility and acceptability of implementing a deprescribing intervention with older people with dementia and their care partners in primary care. The intervention consists of patient-facing educational brochures on CNS-active medications and decision support for the primary care provider. Ethnic/minority groups will be over-sampled to ensure a diverse study sample.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.123 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Services Research Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Older Adult Sample Inclusion Criteria: * Diagnosed dementia (dementia diagnosis code or prescription for dementia medication) * Receiving primary care at a Kaiser Permanente Washington integrated group practice outpatient clinic * Prescribed at least one CNS-active medication on a chronic (3 months or more) basis Exclusion Criteria: * Skilled nursing facility resident * Current cancer diagnosis * On hospice or palliative care Care Partner Sample Inclusion Criteria: * Aged 18 years or older * Self-identify as a care partner for the older adult with dementia
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Kaiser Permanente Health Research Institute
Seattle, United StatesOpen Kaiser Permanente Health Research Institute in Google Maps