Emergency preparedness program for caregivers of dementia patients
Emergency Preparedness and Support for Caregivers of Persons With Dementia: Disaster PrepWise
This study tests a program to help caregivers of dementia patients prepare for emergencies like disasters, so they can manage stress and access resources more easily.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 250 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Iowa Academic / other |
| Locations | 1 site (Iowa City, Iowa) |
| Trial ID | NCT05619263 on ClinicalTrials.gov |
What this trial studies
This program aims to enhance the emergency preparedness of caregivers for individuals with dementia, particularly in the face of disasters such as pandemics and extreme weather events. It focuses on developing actionable caregiving plans to help caregivers manage stress and maintain access to resources during crises. The initiative recognizes the unique vulnerabilities faced by caregivers, especially in rural areas where support may be limited. By implementing the Disaster PrepWise-Caregiver intervention, the program seeks to bolster caregiver resilience and reduce distress.
Who should consider this trial
Good fit: Ideal candidates for this program are English-speaking adults who are family members or friends of individuals diagnosed with Alzheimer's disease or related dementias.
Not a fit: Patients who are in the early stages of cognitive impairment or reside in nursing homes may not benefit from this program.
Why it matters
Potential benefit: If successful, this program could significantly improve the ability of caregivers to manage emergencies, thereby enhancing the well-being of both caregivers and individuals with dementia.
How similar studies have performed: While there is limited data on similar programs specifically targeting dementia caregivers, the increasing focus on emergency preparedness in healthcare suggests a growing recognition of its importance.
Eligibility criteria
Show full inclusion / exclusion 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).
Where this trial is running
Iowa City, Iowa
- University of Iowa — Iowa City, Iowa, United States (Recruiting)
Study contacts
- Principal investigator: Sato Ashida, PhD — University of Iowa
- Study coordinator: Sato Ashida, PhD
- Email: sato-ashida@uiowa.edu
- Phone: 319-384-1477
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.