Dementia Caregiver Career Study
Primary Purpose
Stress, Carer Stress Syndrome, Dementia
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Resourcefulness Training
Biofeedback Training
Diversional Activites
Sponsored by
About this trial
This is an interventional treatment trial for Stress focused on measuring Caregiver, Biofeedback, Resourcefulness, Self-Management
Eligibility Criteria
Inclusion Criteria:
- At least 18 years old
- Have a living family member or a recently deceased family member diagnosed with Alzheimer's disease or another dementia
- Identify self as a primary caregiver
- In-home Caregivers: must be currently providing a minimum of 4 hours per day of supervision/direct care, and have entered that role within the past twelve months; Care Partners whose family member moved into a nursing or assisted living facility within the past twelve months, and must report visiting their care recipient at least once per week; Caretakers (i.e. bereaved) whose family member is deceased within the past twelve months, and are persons with direct oversight of the deceased person's belongings, estate, finances, etc.
- Be capable of performing informed consent and participating in study procedures
Exclusion Criteria:
- Does not have a family member with Alzheimer's disease or another dementia
- Has not cared for a living family member with dementia within the last 12 months, or the family member has been deceased for more than 12 months
- Has knowledge of another family member in the same household enrolled in the study
- Currently pregnant
- Has a pacemaker
- Lives outside of the study area
Sites / Locations
- CWRU School of NursingRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Self-Management
Attention Control Condition
Arm Description
Outcomes
Primary Outcome Measures
Change in Caregiver's Global Health
Change in self-assessment of general physical and mental health, as measured by the Patient-Reported Outcomes Measurement Information System 10-Question Short Form (PROMIS-10 Global Health). Ten items are rated on a five-point scale, scores range from 10-50, and a higher score indicates better health and health-related quality of life.
Change in Caregiver's Health Risk Behavior Scale
9 items; 3-point scale, Scores range 9-27; higher score indicates greater risk
Secondary Outcome Measures
Change in Caregiver's Heart Rate Variability
Changes in the heart rate variability (HRV), as measured through non-invasive heart rate monitoring and scored in standard deviations of milliseconds of fluctuation from average heart rate. While range norms are specific to age and cardiovascular function, higher scores indicate lower levels of stress, and greater adaptability and resilience of the autonomic nervous system in response to stress.
Change in Caregiver's Resourcefulness Scale
28 items; 6-point scale; Scores range 0-140; higher score indicates more resourcefulness
Change in Caregiver's Perceived Stress Scale
14 items; 3-point scale; Scores range 9-27; higher score indicates greater perceived stress
Change in Caregiver's Depressive Cognitions Scales
8 items; 6-point scale; Scores range 0-40; higher score indicates higher depressive cognition
Change in Caregiver's Negative Emotions Checklist
10 items; dichotomous list; Scores range 0-10; higher score indicates more negative emotions.
Full Information
NCT ID
NCT04603482
First Posted
October 21, 2020
Last Updated
December 13, 2022
Sponsor
Case Western Reserve University
1. Study Identification
Unique Protocol Identification Number
NCT04603482
Brief Title
Dementia Caregiver Career Study
Official Title
Self-Management Interventions: Considering Needs & Preferences of Dementia Caregivers
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 8, 2021 (Actual)
Primary Completion Date
January 31, 2024 (Anticipated)
Study Completion Date
January 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Case Western Reserve University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
How do varying levels of participation in selecting self-management interventions (ranging from no input into the selection to selection based on need or preference) affect health risks and physical and mental health over time in family caregivers of persons with Alzheimer's and other dementia disorders? Caregivers will be randomized to 1) information on diversional activities (attention control); 2) self-management intervention based on need (SM-need); or 3) self-management intervention of their preference (SM-preference).
Detailed Description
The study has two aims: The primary aim (A1) is to examine differences across the three groups (attention control, SM-need, and SM-preference) on caregiver health (health risks and mental and physical health) over time. The investigators hypothesize that the caregivers who receive a self-management intervention based on need (SM-need) or preference (SM-preference) will have better health outcomes than those in the attention control.
Secondary aims are to: A2) explore whether caregiver baseline need or preference for intervention (i.e. choice) is associated with: a) care recipient's symptoms; b) caregiver reactions; and c) caregiving involvement, and A3) build caregiver profiles from demographic/ contextual factors that are associated with their needs and preferences for the self-management interventions.
All caregivers will complete assessment measures and measures of health risks, and physical and mental health at baseline (T1), about 6 months (T2), and about 12 months (T3). Caregivers will be randomly assigned to one of three groups. The attention control group will receive information on diversional activities. The SM-need group will receive a self-management intervention for biofeedback training or resourcefulness training, as determined by baseline cut scores. Caregivers in the SM-preference group will choose one of the two self-management interventions according to their personal preference.
Both self-management interventions (biofeedback training, resourcefulness training) and the diversional activities, are delivered over four weeks (between T1 and T2). Caregivers may use the intervention whenever and as often as they wish (i.e. self-tailoring) for the remainder of the study period. These resourcefulness training includes teaching self-help (stress-management, problem-solving) and help-seeking skills, respectively. Biofeedback training consists of the use of a hand-held device that shows the participant their changes in heart rate based on changes in their breathing pattern (as they relax); caregivers who need or prefer the biofeedback will be given a device to use for 28 days. All study participants receiving the intervention will also be asked to keep a journal to record their experience with the intervention.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stress, Carer Stress Syndrome, Dementia, Alzheimer's Disease, Bereavement
Keywords
Caregiver, Biofeedback, Resourcefulness, Self-Management
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
300 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Self-Management
Arm Type
Experimental
Arm Title
Attention Control Condition
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
Resourcefulness Training
Intervention Description
A cognitive-behavioral intervention presented within an audiovisual format that consists of teaching and reinforcing personal (self-help) and social (help-seeking) resourcefulness skills.
Intervention Type
Behavioral
Intervention Name(s)
Biofeedback Training
Intervention Description
Use of a heart-rate variability (HRV) tracking device to enable one to learn to alter physiology to improve health. Devices are used to measure physiological activity, e.g., breathing and heart function, and provide rapid, accurate "feedback" to the user, thereby enabling desired physiological changes that can endure over time without continued use of the device and to continue to influence behavior.
Intervention Type
Behavioral
Intervention Name(s)
Diversional Activites
Intervention Description
An audiovisual format presenting 12 activities for adults including but not limited; crossword puzzles, reading, gardening, exercise, cooking/baking, board games, learning a new language, social activities, online games, etc.
Primary Outcome Measure Information:
Title
Change in Caregiver's Global Health
Description
Change in self-assessment of general physical and mental health, as measured by the Patient-Reported Outcomes Measurement Information System 10-Question Short Form (PROMIS-10 Global Health). Ten items are rated on a five-point scale, scores range from 10-50, and a higher score indicates better health and health-related quality of life.
Time Frame
From T1 (baseline) to T2 (6 months) through T3 (one year)
Title
Change in Caregiver's Health Risk Behavior Scale
Description
9 items; 3-point scale, Scores range 9-27; higher score indicates greater risk
Time Frame
From T1 (baseline) to T2 (6 months) through T3 (one year)
Secondary Outcome Measure Information:
Title
Change in Caregiver's Heart Rate Variability
Description
Changes in the heart rate variability (HRV), as measured through non-invasive heart rate monitoring and scored in standard deviations of milliseconds of fluctuation from average heart rate. While range norms are specific to age and cardiovascular function, higher scores indicate lower levels of stress, and greater adaptability and resilience of the autonomic nervous system in response to stress.
Time Frame
From T1 (baseline) to T2 (6 months) through T3 (one year)
Title
Change in Caregiver's Resourcefulness Scale
Description
28 items; 6-point scale; Scores range 0-140; higher score indicates more resourcefulness
Time Frame
From T1 (baseline) to T2 (6 months) through T3 (one year)
Title
Change in Caregiver's Perceived Stress Scale
Description
14 items; 3-point scale; Scores range 9-27; higher score indicates greater perceived stress
Time Frame
From T1 (baseline) to T2 (6 months) through T3 (one year)
Title
Change in Caregiver's Depressive Cognitions Scales
Description
8 items; 6-point scale; Scores range 0-40; higher score indicates higher depressive cognition
Time Frame
From T1 (baseline) to T2 (6 months) through T3 (one year)
Title
Change in Caregiver's Negative Emotions Checklist
Description
10 items; dichotomous list; Scores range 0-10; higher score indicates more negative emotions.
Time Frame
From T1 (baseline) to T2 (6 months) through T3 (one year)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
At least 18 years old
Have a living family member or a recently deceased family member diagnosed with Alzheimer's disease or another dementia
Identify self as a primary caregiver
In-home Caregivers: must be currently providing a minimum of 4 hours per day of supervision/direct care, and have entered that role within the past twelve months; Care Partners whose family member moved into a nursing or assisted living facility within the past twelve months, and must report visiting their care recipient at least once per week; Caretakers (i.e. bereaved) whose family member is deceased within the past twelve months, and are persons with direct oversight of the deceased person's belongings, estate, finances, etc.
Be capable of performing informed consent and participating in study procedures
Exclusion Criteria:
Does not have a family member with Alzheimer's disease or another dementia
Has not cared for a living family member with dementia within the last 12 months, or the family member has been deceased for more than 12 months
Has knowledge of another family member in the same household enrolled in the study
Currently pregnant
Has a pacemaker
Lives outside of the study area
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jaclene A Zauszniewski, PhD
Phone
216-368-3612
Email
jaz@case.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Evelina DiFranco, MPH
Email
exd138@case.edu
Facility Information:
Facility Name
CWRU School of Nursing
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Evelina DiFranco, MPH
12. IPD Sharing Statement
Learn more about this trial
Dementia Caregiver Career Study
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