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Not yet recruitingNCT07163715FALL-ADLUpdated Sep 9, 2025

Incidence and Factors of Functional Decline After Emergency Department Discharge in Older Adults With Falls

An observational study in Fall, Daily Activities and Functional Decline, sponsored by Ege University. Not yet recruiting. Open to participants aged 65 Years and older. Per ClinicalTrials.gov, last updated 2025-09-09.

Sponsored by Ege University · Observational

From the registry’s dates

  • Primary completion was expected by Nov 2025, 11 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
280
Ages
65 Years and older
Sex
All
01

Study summary

The goal of this observational study is to learn about changes in activities of daily living (ADL) in older adults after being discharged from the emergency department (ED) following a fall.

The main questions this study aims to answer are:

How often do older adults experience a decline in their ability to perform daily activities after being discharged from the ED for a fall? What health or lifestyle factors (such as frailty, medications, physical activity, or fear of falling) are related to this decline? Participants will be 65 years or older, admitted to the ED for a simple fall, and discharged without hospitalization. At the time of their ED visit, participants will be asked questions about their health, medications, activity level, and daily functioning. They will then be contacted online or by phone at 7 days and 30 days after discharge to answer follow-up questions.

This study will help identify how common functional decline is after falls in older adults discharged from the ED, and which factors may predict higher risk. These findings could help improve follow-up care and prevention strategies for older patients.

Read the detailed description

Falls are one of the leading causes of morbidity and functional decline in older adults. Even in cases without major injury requiring hospitalization, falls can lead to decreased independence and reduced quality of life. Functional decline, often measured as deterioration in activities of daily living (ADL), is associated with frailty, multimorbidity, polypharmacy, fear of falling, and reduced physical activity. Early identification of older patients at risk for functional decline after an emergency department (ED) visit is critical for designing timely interventions and improving patient outcomes.

This prospective cohort study will enroll 280 patients aged 65 years and older who present to the ED with a simple fall and are discharged without hospitalization. Baseline data will be collected at the time of ED visit, including demographic characteristics, comorbidities, medication use, frailty status (Clinical Frailty Scale), physical activity level (Physical Activity Scale for the Elderly, PASE), fall risk (MEFRAT), and fear of falling (Falls Efficacy Scale-International, FES-I). ADL status will be assessed at baseline and re-assessed at 7 and 30 days after discharge through online or telephone interviews.

The primary outcome is the incidence of decline in ADL within 30 days after ED discharge. Secondary analyses will examine associations between demographic, clinical, functional, and psychosocial factors and the risk of ADL decline, using logistic regression models.

The study is expected to provide valuable insights into the frequency and determinants of functional decline among older adults after ED discharge for falls. Identifying these risk factors will inform strategies for early recognition, follow-up care, and targeted interventions aimed at preventing functional decline and maintaining independence in older patients.

02

Conditions studied

  • Fall
  • Daily Activities
  • Functional Decline
  • Older Adults (65 Years and Older)

Keywords

  • Falls
  • Decline fictional status
  • Decline daily activities
  • Emergency medicine
03

In context

Lead sponsor

Ege University is the lead sponsor of 365 studies on the registry; 46 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
65 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

The study population will consist of community-dwelling older adults aged 65 years and older who present to the emergency department (ED) with a simple fall and are discharged without hospitalization. Participants must be cognitively able to complete baseline and follow-up assessments.

This population represents a group at risk of functional decline despite not requiring inpatient admission. By focusing on older adults discharged from the ED, the study aims to capture real-world outcomes in a population that is often underrepresented in research but commonly experiences falls and subsequent declines in independence.

Inclusion criteria

  • Age ≥ 65 years
  • Presentation to the emergency department with a simple (non-injurious) fall
  • Discharged from the ED without hospitalization
  • Cognitively able to answer online or telephone follow-up interviews

Exclusion criteria

Exclusion Criteria:

  • Falls due to traumatic events other than simple falls
  • Hospital admission required after the fall
  • Presence of acute confusion, dementia, or other severe cognitive impairment
  • Inability to access online or telephone follow-up during the 30-day study period
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
280 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Decline in Activities of Daily Living

    Change in Activities of Daily Living (ADL) score from baseline to follow-up. Decline is defined as an increase in dependency in at least one ADL item compared with baseline.

    Time frame: Baseline (ED discharge), 7 days, and 30 days after discharge

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 9, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07163715
Lead sponsor
Ege University
Responsible party
Ozge Can. MD (MD, Ege University) — Principal investigator
First posted
Sep 9, 2025
Start date
Sep 5, 2025 (estimated)
Primary completion
Nov 5, 2025 (estimated)
Completion
Dec 5, 2025 (estimated)
Last update
Sep 9, 2025

Study contacts

Özge Can
Contact
ozgece83@gmail.com
+905054499887 ext. 5057521845
Şadiye Mıdık
Contact
sadiyeayhan@hotmail.com

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2025. You cannot join it, but the record below documents what was studied.

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