Shed-MEDS Deprescribing for Dementia
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to reduce the use of unnecessary or potentially harmful medications in people with dementia living in assisted living facilities. The focus is on safely lowering doses or stopping certain medications, based on expert advice and patient or representative preferences. Researchers will monitor how many medications are reduced and whether quality of life improves over 90 days. Individuals with dementia who live in an assisted living facility and take five or more medications, or at least one potentially unsuitable medication, are well-suited for this trial. As an unphased trial, this study offers participants the chance to contribute to important research that could enhance medication management and quality of life for people with dementia.
Will I have to stop taking my current medications?
The trial aims to reduce or stop unnecessary or potentially harmful medications for participants with dementia. This means you might need to stop or reduce some of your current medications, based on clinical guidelines and your preferences.
What prior data suggests that this deprescribing intervention is safe for residents with dementia?
Research has shown that the Shed-MEDS deprescribing method is safe. In several studies, this approach helped people reduce their medication count without harm. These studies found that patients could safely stop or lower their medication doses. Importantly, no major negative effects were reported, making it a well-tolerated option for reducing unnecessary medications.12345
Why are researchers excited about this trial?
Researchers are excited about the Shed-MEDS Deprescribing Intervention because it offers a personalized approach to managing medications for individuals with dementia. Unlike traditional treatments that often focus on adding medications, this intervention emphasizes safely reducing or stopping medicines based on clinical criteria and patient preferences. This method could potentially minimize medication-related side effects and improve overall quality of life for patients, making it a promising alternative to the usual medication-heavy approach in dementia care.
What evidence suggests that the Shed-MEDS Deprescribing Intervention is effective for dementia?
Research has shown that the Shed-MEDS Deprescribing Intervention, which participants in this trial will receive, helps reduce unnecessary medications in older adults. One study found that this approach safely lowered the number of medications without harming patients. For people with dementia, reducing medications can improve quality of life by minimizing the risk of side effects from unnecessary drugs. The intervention involves reviewing a patient's medications and suggesting which ones can be reduced or stopped, based on medical advice and patient preferences. This method has shown promise in enhancing well-being by focusing on essential medications.12346
Are You a Good Fit for This Trial?
This trial is for English-speaking residents with dementia at Abe's Garden assisted living facility, who are on five or more medications or taking medication that may not be suitable (as defined by specific criteria). They must be able to consent themselves or have someone who can consent for them.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Intervention
Participants undergo a deprescribing intervention to reduce unnecessary or potentially harmful medications
Follow-up
Participants are monitored for safety and effectiveness after the intervention
What Are the Treatments Tested in This Trial?
Interventions
- Shed-MEDS Deprescribing Intervention
Shed-MEDS Deprescribing Intervention is already approved in United States for the following indications:
- Polypharmacy reduction in older adults transitioning from hospital to post-acute care facilities
- Deprescribing for dementia care in assisted living facilities
Find a Clinic Near You
Who Is Running the Clinical Trial?
Vanderbilt University
Lead Sponsor
National Institute on Aging (NIA)
Collaborator