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Dementia Home Care Intervention for Dementia
Richmond, VA
N/A
Waitlist Available
Led By Christine S Ritchie, MD, MSPH
Research Sponsored by Massachusetts General Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up post-intervention (6 months)
Awards & highlights
No Placebo-Only Group
Summary
This trial will develop an intervention to improve care for people living with dementia and their caregivers in home-based primary care practices.
Who is the study for?
This trial is for adult caregivers living in the U.S. who provide at least 4 hours of daily care to someone with Alzheimer's or related dementias and are experiencing stress. Participants must speak English and expect to continue caregiving for the next 6 months. Staff participants should be part of a home-based primary care program.
What is being tested?
The study aims to develop 'Dementia Care Quality at Home' for those with dementia and their caregivers, assessing its feasibility, acceptability, and fidelity within home-based primary care practices through an open-pilot trial involving trained clinicians.
What are the potential side effects?
Since this intervention focuses on caregiver support rather than medical treatment, traditional side effects are not applicable. However, there may be emotional or psychological impacts from participating in focus groups or implementing new care strategies.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ post-intervention (6 months)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~post-intervention (6 months)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Feasibility for the caregiver to access educational materials and community resources.
Feasibility for the caregiver to engage with and complete baseline assessments.
Feasibility for the practice of assessing eligible patient/caregiver dyads.
+2 moreOther study objectives
Acceptability of the intervention to caregivers and patient to participate in the intervention.
Caregiver well-being
Feasibility for the practice of clinicians to engage with the tele-video case conference.
+5 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Dementia Care Quality at HomeExperimental Treatment1 Intervention
Each HBPC practice will receive the Dementia Care Quality at Home intervention.
Find a Location
Closest Location:Virginia Commonwealth University· Richmond, VA
Who is running the clinical trial?
Massachusetts General HospitalLead Sponsor
3,061 Previous Clinical Trials
13,425,685 Total Patients Enrolled
26 Trials studying Dementia
202,627 Patients Enrolled for Dementia
Retirement Research FoundationOTHER
9 Previous Clinical Trials
1,706 Total Patients Enrolled
1 Trials studying Dementia
50 Patients Enrolled for Dementia
Christine S Ritchie, MD, MSPHPrincipal InvestigatorMassachusetts General Hospital
2 Previous Clinical Trials
524 Total Patients Enrolled
1 Trials studying Dementia
13 Patients Enrolled for Dementia
Bruce Leff, MDPrincipal InvestigatorJohns Hopkins University
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am under 18 years old.I provide at least 4 hours of daily care or supervision.I live with and care for someone with Alzheimer's or related dementia.I am 18 years old or older.I am an adult caregiver aged 18 or older.
Research Study Groups:
This trial has the following groups:- Group 1: Dementia Care Quality at Home
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.