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Caring for Caregivers and People Living With Dementia Under Home-Based Primary Care

Primary Purpose

Dementia, Quality of Life, Caregiver Stress

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Dementia Care Quality at Home
Sponsored by
Massachusetts General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Dementia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Caregiver participants will: be adults (18 years or older) have English fluency and literacy live in the United States live with and care for an individual with Alzheimer's Disease and Alzheimer's Disease Related Dementias (ADRD) anticipate providing care for the next 6 months provide an average 4 hours of supervision or direct assistance per day for the care recipient and have been identified by the practice as experiencing caregiver stress. Staff participants will: be 18 years or older have English fluency and literacy and live in the United States and be part of a HBPC primary care program or closely connected to the practice. Exclusion Criteria: Participants under the age 18. Participants who have no English fluency and literacy and do not live in the United States. For caregiver participants, not caring for and living with a patient that is part of a HBPC primary care program or closely connected to the practice.

Sites / Locations

  • Queens Medical CenterRecruiting
  • Virginia Commonwealth UniversityRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Dementia Care Quality at Home

Arm Description

Each HBPC practice will receive the Dementia Care Quality at Home intervention.

Outcomes

Primary Outcome Measures

Feasibility for the caregiver to engage with and complete baseline assessments.
The percentage of identified CGs who complete baseline assessments.
Feasibility for the caregiver to access educational materials and community resources.
Percent of CGs will report using 1 or more materials provided by the practice.
Feasibility for the practice of identifying potential patients/caregivers
Ability of practice to generate list of their patients living with dementia using a questionnaire to the practice
Feasibility for the practice of assessing eligible patient/caregiver dyads.
Ability of practice to identify eligible patient/caregiver dyads (e.g., CG experiencing burden or distress).
Feasibility for the practice to use patient and caregiver assessments.
Percent of practice personnel who conduct assessments that rate assessments as feasible to use and percent of audited assessments that are completed.

Secondary Outcome Measures

Full Information

First Posted
April 7, 2023
Last Updated
October 16, 2023
Sponsor
Massachusetts General Hospital
Collaborators
Retirement Research Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT05849259
Brief Title
Caring for Caregivers and People Living With Dementia Under Home-Based Primary Care
Official Title
Caring for Caregivers and People Living With Dementia Under Home-Based Primary Care
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 16, 2023 (Actual)
Primary Completion Date
July 2024 (Anticipated)
Study Completion Date
September 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital
Collaborators
Retirement Research Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this clinical trial is to develop a dementia care intervention for persons receiving home-based primary care (HBPC) and living with dementia (PLWD) and their caregivers, and test the feasibility of implementing the intervention in HBPC practices to ultimately improve outcomes of PLWD and their caregivers. The main aims are to: Develop and refine HBPC Dementia Care Quality at Home Establish feasibility (primary outcome), acceptability, and fidelity of HBPC Dementia Care Quality at Home through an open-pilot trial involving two HBPC practices. Trained clinicians and staff at two HBPC practices will implement the intervention Relevant stakeholders (caregivers of PLWD, and HBPC clinicians and staff) will participate in qualitative focus groups to provide feedback on the intervention.
Detailed Description
The overarching goal of this project is to develop a dementia care intervention for PLWD and their caregivers, Dementia Care Quality at Home, and test the feasibility of implementing the intervention in two HBPC practices to ultimately improve outcomes of PLWD and their caregivers. The investigators will evaluate the feasibility, acceptability, and fidelity in implementing HBPC Dementia Care Quality at Home in two practices for persons living with dementia and their caregivers through an open pilot. Hypothesis: HBPC Dementia Care Quality at Home will meet benchmarks of feasibility, acceptability, and fidelity by the HBPC practices implementing it and by caregivers of PLWD who experience the intervention. The investigators will assess feasibility of caregivers of PLWD to engage with the intervention, the acceptability of the intervention to caregivers, and the impact of the intervention on caregiver well-being by surveying caregivers at the conclusion of the pilot. In addition, the investigators will assess feasibility, acceptability, and fidelity of the intervention in the practices.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dementia, Quality of Life, Caregiver Stress

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
A live open-pilot trial will be conducted of the HBPC Dementia Care Quality at Home intervention in two HBPC practices.
Masking
None (Open Label)
Allocation
N/A
Enrollment
98 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Dementia Care Quality at Home
Arm Type
Experimental
Arm Description
Each HBPC practice will receive the Dementia Care Quality at Home intervention.
Intervention Type
Other
Intervention Name(s)
Dementia Care Quality at Home
Intervention Description
Each of the two HBPC practices will identify at least two trained Dementia Care Quality at Home Champions who will be trained in the intervention comprised of 1) a standardized assessment tool to assess PLWD and caregiver needs; 2) seven modules created to optimize the well-being of the PLWD and their caregiver; and 3) regular team-based review of persons participating in the program to address care challenges and a team-based case conference approach to solve these challenges.
Primary Outcome Measure Information:
Title
Feasibility for the caregiver to engage with and complete baseline assessments.
Description
The percentage of identified CGs who complete baseline assessments.
Time Frame
Baseline
Title
Feasibility for the caregiver to access educational materials and community resources.
Description
Percent of CGs will report using 1 or more materials provided by the practice.
Time Frame
Post-intervention (6 months)
Title
Feasibility for the practice of identifying potential patients/caregivers
Description
Ability of practice to generate list of their patients living with dementia using a questionnaire to the practice
Time Frame
Baseline
Title
Feasibility for the practice of assessing eligible patient/caregiver dyads.
Description
Ability of practice to identify eligible patient/caregiver dyads (e.g., CG experiencing burden or distress).
Time Frame
Baseline
Title
Feasibility for the practice to use patient and caregiver assessments.
Description
Percent of practice personnel who conduct assessments that rate assessments as feasible to use and percent of audited assessments that are completed.
Time Frame
Post-intervention (6 months)
Other Pre-specified Outcome Measures:
Title
Feasibility for the practice of recruiting patient/caregiver dyads
Description
Percentage of eligible dyads who enroll.
Time Frame
Post-intervention (6 months)
Title
Feasibility for the practice of percent of racial and ethnic minorities recruited.
Description
Percentage of eligible dyads who enroll who are racial and ethnic minorities.
Time Frame
Post-intervention (6 months)
Title
Feasibility for the practice to use care modules.
Description
The percentage that rates modules as feasible to use. The percentage of practice personnel who complete the modules that rate the modules as feasible to use and the percent of audited modules that are completed.
Time Frame
Post-intervention (6 months)
Title
Feasibility for the practice of clinicians to engage with the tele-video case conference.
Description
Percent of virtual meetings attended.
Time Frame
Post-intervention (6 months)
Title
Net promoter score
Description
The single question - "How likely are you to recommend X to a friend [or colleague]?" is rated from 0 - Not at all likely to 10 - Extremely likely.
Time Frame
Post-intervention (6 months)
Title
Acceptability of the intervention to caregivers and patient to participate in the intervention.
Description
Percent of CGs invited to participate who agree to participate in the intervention.
Time Frame
Post-intervention (6 months)
Title
Heard and understood
Description
A one-item measure of CGs who report that they felt heard and understood by the practice.
Time Frame
Pre and post intervention (prior to and 6 months after)
Title
Caregiver well-being
Description
Quality of Life in Alzheimer's Disease. The QoL-AD is comprised of 13 items (physical health, energy, mood, living situation, memory, family, marriage, friends, self as a whole, ability to do chores, ability to do things for fun, money and life as a whole). Response options include 1(poor), 2(fair), 3(good) and 4 (excellent), for a total score of 13-52, with higher scores indicating better QoL.
Time Frame
Post-intervention (6 months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Caregiver participants will: be adults (18 years or older) have English fluency and literacy live in the United States live with and care for an individual with Alzheimer's Disease and Alzheimer's Disease Related Dementias (ADRD) anticipate providing care for the next 6 months provide an average 4 hours of supervision or direct assistance per day for the care recipient and have been identified by the practice as experiencing caregiver stress. Staff participants will: be 18 years or older have English fluency and literacy and live in the United States and be part of a HBPC primary care program or closely connected to the practice. Exclusion Criteria: Participants under the age 18. Participants who have no English fluency and literacy and do not live in the United States. For caregiver participants, not caring for and living with a patient that is part of a HBPC primary care program or closely connected to the practice.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Maimouna Sy, BS
Phone
617-643-9070
Email
masy@mgh.harvard.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Michelle St. Paul, MA
Phone
781-771-5495
Email
mstpaul2@mgh.harvard.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christine S Ritchie, MD, MSPH
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Bruce Leff, MD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Queens Medical Center
City
Honolulu
State/Province
Hawaii
ZIP/Postal Code
96813
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jacob W Moore, NP
Email
jamoore@queens.org
Facility Name
Virginia Commonwealth University
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23219
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kathryn Rackson, MD
Email
kathryn.rackson@vcuhealth.org

12. IPD Sharing Statement

Plan to Share IPD
No
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Caring for Caregivers and People Living With Dementia Under Home-Based Primary Care

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