In the US, the over 11 million Americans currently providing unpaid care to a family member, relative, or friend with Alzheimer's disease or a related dementia (ADRD) are over 6 times more likely than the general population to suffer from depression (33.9% vs. 5%), and nearly 60% rate their emotional distress as high or very high. The purpose of this Phase II research is to continue the successful work of the pilot development and testing by conducting a rigorous scientific study of the effects of Compass for Care, a digital program that customizes behavior change guidance for using five self-care behaviors critical to ADRD caregiver well-being: 1) taking time to recharge; 2) finding information about your loved one's diagnosis and needs; 3) discovering your strengths and limits; 4) exploring outside help; and 5) seeking emotional support.
The efficacy of the Compass for Care intervention is being tested in a randomized trial involving up to 305 caregivers caring for a family member or friend with Alzheimer's disease or a related dementia (ADRD). Caregivers who meet study inclusion criteria (e.g., being an ADRD caregiver caring for a family member or friend for 8+ hours/week, residing in the US, agreeing to receive daily text or email messages for three months, not indicating suicidal ideation, and experiencing a level of caregiver burden) as assessed in on online screening survey, are invited to participate in the study. Caregivers are randomly assigned to either the treatment or attention control condition. The treatment group is provided access to the 12-week Compass for Care mobile first program and attention control group is provided access to a 12-week mobile optimized intervention focused on safety behaviors. Both interventions are delivered in weekly modules and include daily messages delivered by email or text message. Follow-up assessments are conducted online at 3, 6, and 9 months. Outcomes include caregiver burden, depression, perceived stress, emotional and physical health, life satisfaction, resilience, and well-being. Study protocols include best practices for maximizing retention at follow-up in research.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
305
Participants receive 12 weekly modules containing interactive activities and static content and tailored messages delivered via text message or email. The intervention focuses on five self-care behaviors critical to ADRD caregiver well-being: 1) taking time to recharge; 2) finding information about your loved one's diagnosis and needs; 3) discovering your strengths and limits; 4) exploring outside help; and 5) seeking emotional support.
Participants receive 12 weekly modules and tailored messages delivered via text message or email. The intervention focuses on safety behaviors (e.g., weather safety, first aid, home safety, etc.)
Pro-Change Behavior Systems
Narragansett, Rhode Island, United States
Zarit Burden Interview (ZBI)
Developed from the 29 and 22-item versions, this shortened 12-item Zarit Burden Interview measure assesses subjective burden among caregivers of individuals with dementia. Caregivers are asked to rate items (e.g., Do you feel… that your health has suffered because of your involvement with your relative?) on a 5-point scale with 0 = never to 4 = nearly always. Cronbach's alpha is .88.
Time frame: Baseline, 3, 6, and 9 months' follow-up
Patient Health Questionaire (PHQ-9)
Depression is being assessed using the PHQ-9, which asks the number of days in the past two weeks the respondent had experienced each of the Diagnostic and Statistical Manual (DSM) symptoms of depression, minus suicidality. Response options are 0 = Not at all, 1 = Several days, 2 = More than half the days, and 3 = Nearly every day. Scores are summed to produce a total score, and a PHQ-9 cutpoint ≥ 10 is used to define moderate to severe depression. Both depression symptoms (i.e., total score) and prevalence of current depression (score \> 10) will be examined in this study.
Time frame: Baseline, 3, 6, and 9 months' follow-up
Resilience Evaluation Measure (REM-3)
Developed by ProChange, this 3-item survey assesses three key drivers of resilience: mindset, meaning, and social connections. Items are rated on a 5-point scale with 1 = never, 2 = rarely, 3 = sometimes, 4 = often, and 5 = almost always. Cronbach's alpha is .81.
Time frame: Baseline, 3, 6, and 9 months' follow-up
World Health Organization Well-Being Index (WHO-5)
The WHO-5 is a widely used measure that assesses well-being. Respondents are asked to rate five items (e.g., I have felt calm and relaxed) in relation to how they've felt over the last two weeks. Responses range on a 6-point scale from 0=At no time to 5=All of the time.
Time frame: Baseline, 3, 6, and 9 months' follow-up
Cohen's Perceived Stress
Originally developed in 1983, the Perceived Stress Scale (PSS) includes 10 items (e.g., In the last month, how often have you felt that you were unable to control the important things in your life) focused on varied situations. Respondents rate the items on a 5-point scale ranging from 0 = never to 4 = very often.
Time frame: Baseline, 3, 6, and 9 months' follow-up
Perceived Change Index
This measure of well-being assesses factors associated with increased risk for adverse emotional and physical outcomes among caregivers. Caregivers are asked to rate 13 items (e.g., ability to manage day to day) on a 5- point scale with 1 = became much worse to 5 = improved a lot over the past month. Negatively worded items are reversed scored and an overall measure mean is computed. Cronbach's alpha is .88.
Time frame: Baseline, 3, 6, and 9 months' follow-up
Cantril/Gallup Life Evaluation Index
In its World Poll administered in 150 countries, Gallup, Inc. uses the 2-item Cantril Self-Anchoring Scale and a simple scoring algorithm to assess subjective well-being. Respondents are asked to rate their current life-and then to rate their future life, "say about five years from now"-on a ladder where 0 represents the worst possible life and 10 best possible life. Individuals who rate their current life a "7" or higher AND their future life an "8" or higher are classified as "thriving." Individuals who rate their current and future lives a "4" or lower are classified as "suffering." All others are "struggling." Previous research has shown that those classified as thriving experience less depressive symptoms, higher physical and emotional health and have fewer health risk behaviors than those in struggling and suffering.
Time frame: Baseline, 3, 6, and 9 months' follow-up
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