Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05619263 · ClinicalTrials.gov registry record · NA

Emergency Preparedness for Caregivers of Persons With Dementia: Disaster PrepWise

A NA study of Caregiver Resilience and Stress, sponsored by Sato Ashida.

Recruiting
Registry status
NA
Development phase
250
Enrollment target
1
Study location

NCT05619263: Recruiting NA study of Caregiver Resilience and Stress, sponsored by Sato Ashida.

NCT05619263 is a NA study of Caregiver Resilience and Stress that is actively recruiting participants, run by Sato Ashida. The registered enrollment target is 250 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (82% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05619263, a NA study of Caregiver Resilience and Stress, is actively recruiting participants, sponsored by Sato Ashida.

RECRUITING
Registry status
NA
Development phase
250 participants
Enrollment target
1
Study location

Study 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 wi

Primary Outcome

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

Interventions

  • BEHAVIORAL Disaster PrepWise-Caregiver

Study Locations (1)

Iowa

  • University of Iowa - Iowa City

Trial Details

FieldValue
Enrollment Target 250 participants
Start Date 2023-07-12
Est. Completion 2027-06-30
Phase NA
Sato Ashida

2 total trials

What NCT05619263 shows while recruiting

NCT05619263 is an interventional study that assigns participants to a tested intervention. The registered 250 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (82% lower).

The record links to 1 condition, with Caregiver Resilience and Stress appearing as the primary indexed condition, and to 1 intervention - of which Disaster PrepWise-Caregiver is the first listed.

NCT05619263 reports a single indexed study location in Iowa.

Frequently Asked Questions

What is clinical trial NCT05619263 about?

NCT05619263 is a clinical study titled "Emergency Preparedness for Caregivers of Persons With Dementia: Disaster PrepWise". 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 ...

What is the current status of trial NCT05619263?

This trial is currently recruiting. It is a NA study. The enrollment target is 250 participants. The study started on 2023-07-12. Estimated completion is 2027-06-30.

What conditions does trial NCT05619263 study?

This clinical trial studies the following conditions: Caregiver Resilience and Stress.

What interventions are being tested in trial NCT05619263?

The interventions under investigation include: Disaster PrepWise-Caregiver (BEHAVIORAL).

Who is sponsoring clinical trial NCT05619263?

This trial is sponsored by Sato Ashida, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05619263 being conducted?

This trial has 1 study location across Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT05619263's enrollment target sits among peer trials

250 410th of 2000 higher than 1,567 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00483249 · 250 participants · NA

    Endovascular Exclusion of Thoracoabdominal and/or Paravisceral Abdominal Aortic Aneurysm

  • NCT00777712 · 250 participants

    Mechanisms Underlying Impaired Diabetic Wound Healing

  • NCT01451502 · 250 participants · NA

    Infusion of Cell Populations From Unlicensed Umbilical Cord Blood Units

  • NCT01771718 · 250 participants

    Pilot Study on In-vivo Non-invasive Skin Imaging Using Multiphoton Microscopy

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05619263, the US trial registry maintained by the National Library of Medicine. NCT05619263 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.