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Clinical Trials/NCT05619263
NCT05619263
Recruiting
Not Applicable

Emergency Preparedness and Support for Caregivers of Persons With Dementia: Disaster PrepWise

Sato Ashida1 site in 1 country250 target enrollmentJuly 12, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Caregiver Resilience and Stress
Sponsor
Sato Ashida
Enrollment
250
Locations
1
Primary Endpoint
Resilience
Status
Recruiting
Last Updated
7 months ago

Overview

Brief Summary

Individuals with dementia and their families are especially vulnerable during a disaster as it limits caregivers' ability to continue with care due to disaster related stress and reduced access to resources and support. The COVID-19 pandemic showed the extreme vulnerability of persons with dementia (PWD) and their caregivers as they struggled to access support and resources due to the threat of COVID-19 infection; such impact was exacerbated in rural areas where caregivers are geographically isolated and disaster management resources are scarce. With the number of federally declared disasters increasing dramatically over the past 50 years, active public health efforts are needed to support caregivers in developing emergency caregiving plans usable in disasters such as pandemics and extreme weather emergencies. The long-term goal of this project is to enhance emergency preparedness and support networks of caregivers of PWD to increase their resilience and minimize distress by implementing an intervention program, Disaster PrepWise (DPW). In the DPW program, a trained Medical Reserve Corp (MRC) volunteer will provide step-by-step guidance to caregivers to jointly develop emergency preparedness plans and personal support networks. The objectives of this proposed study are to 1) test the impact of DPW on caregiver outcomes (i.e., resilience, stress) and perceptions that may mediate the association between DPW and outcomes (caregiver self-efficacy, preparedness, social support); and 2) evaluate implementation strategies in a real-world setting to optimize future dissemination. We will conduct a randomized control trial of 250 caregivers of persons with dementia involving two arms: DPW intervention group and an information-only control group (print information on disaster preparedness). Assessments will occur before randomization (baseline), and 3 and 6 months after the baseline. This study is innovative in its use of a highly personalized disaster preparedness program with built-in assistance to support caregivers; the support will be provided through an existing national-level public health infrastructure (MRC) that has a great potential to reach older adults and caregivers in rural areas. The knowledge and data obtained through this study will lay the foundation for a future larger-scale multi-state pragmatic trial to assess dissemination potentials.

Registry
clinicaltrials.gov
Start Date
July 12, 2023
End Date
June 30, 2027
Last Updated
7 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Sato Ashida
Responsible Party
Sponsor Investigator
Principal Investigator

Sato Ashida

Professor

University of Iowa

Eligibility Criteria

Inclusion Criteria

  • English speaking adults (18 years and older)
  • Family members (e.g., biological and non-biological relatives, friends) of individuals diagnosed with ADRD regardless of whether they live with the individual or not. Individuals will not be excluded based on race/ethnicity, gender, or sexual orientation.

Exclusion Criteria

  • Families of those diagnosed as predementia or mild cognitive impairment are excluded from the parent study due to differing care needs.
  • DPW addresses the needs of community-dwelling individuals, thus, caregivers of those living in nursing homes facilities will be excluded.
  • Caregivers with physical or cognitive conditions that prevent them from consenting or providing responses to questions will be excluded following evaluation ("Evaluation to Sign an Informed Consent Document for Research," UI IRB).

Outcomes

Primary Outcomes

Resilience

Time Frame: Change between baseline and 6-month follow-up

Connor-Davidson Resilience Scale (CD-RISC: 25 items). The range is 0 to 100. Higher scores indicate higher resilience.

Caregiver stress

Time Frame: Change between baseline and 6-month follow-up

Cohen Perceived Stress Scale (PSS: 14 items). The range is 0 to 40. Higher scores indicate higher perceived stress.

Secondary Outcomes

  • Self-Efficacy(Change between baseline and 6-month follow-up)
  • Caregiver Preparedness(Change between baseline and 6-month follow-up)
  • Social Networks(Change between baseline and 6-month follow-up)

Study Sites (1)

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