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NCT07563270Not yet recruiting

GAPcareAD: A Brief Emergency Department Intervention to Address Post-Fall Care Needs of Persons Living With Dementia and Care Partners

Source: ClinicalTrials.gov · Last updated 15 May 2026

Brief summary (registry, in English)

Persons living with dementia (PLWD) are at significantly increased risk for falls, which are the leading cause of emergency department (ED) visits in this population and contribute to serious injuries, functional decline, and caregiver burden. GAPcareAD is an ED-initiated, caregiver-inclusive intervention designed to address fall risk at the point of care. This multi-site trial will compare GAPcareAD (intervention) to usual care for 350 PLWD and caregivers after a fall.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
700 (estimated)
First submitted
10 Apr 2026
Start date
30 Sept 2026
Primary completion date
30 Mar 2029
Lead sponsor
University of Colorado, Denver
NCT number
NCT07563270

What you commit to

  • Study type: Interventional
  • Planned participants: 700
  • From 30 Sept 2026 to the primary completion date, 30 Mar 2029
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients who have advanced cancer and/or are in hospice

Other

  • Living in a nursing home
  • Patients are admitted to the hospital
  • Patients have presence of injuries that prevent mobilization (i.e. pelvic or lower extremity fractures)

Who the study is looking for

  • Community-dwelling adult (living at home or assisted living) 65 years-old or older presenting to ED after a fall within the last seven days
  • Fall not due to syncope or external force (i.e., struck by car,assault, intoxication)
  • Fall not due to serious illness (i.e., stroke, acute myocardial infarction)
  • Patients have an identified caregiver
  • Patient must have known ADRD or score ≥2 on the AD8 Dementia Interview.
  • Anticipated to be discharged to home/assisted living/rehabilitation at the time of consent (i.e. not admitted)
  • The patient and/or caregiver have a reliable phone number where they can be reached throughout the intervention

Age in the registry: 65 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.