- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03076593
GAPcare Fall Prevention Pilot Survey
September 20, 2021 updated by: Rhode Island Hospital
GAPcare: The Geriatric Acute and Post-acute Care Coordination Program - Pilot Survey
GAPcare (Geriatric Acute & Post-acute Care Coordination Program for Fall Prevention) is an early stage investigation that surveys older adults who present to the Emergency Department for any illness to determine the feasibility of an Emergency Department (ED)-based multidisciplinary intervention for preventing recurrent falls in older adults.
In this observational study, older adults will be approached during routine clinical care in the ED and asked about prior falls, prior experiences having falls treated in the inpatient and outpatient setting, and the investigators will solicit feedback on potential improvement to care in the ED setting for falls.
Study Overview
Study Type
Observational
Enrollment (Actual)
82
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Rhode Island
-
Providence, Rhode Island, United States, 02903
- Rhode Island Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
65 years and older (Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Older adults presenting to the Emergency Department at Rhode Island Hospital for any indication
Description
Study inclusion criteria for GAPcare
- Adult 65 years-old or older
- Able to communicate in English
- No cognitive impairment (≥4 on SIS)
Exclusion criteria
• Unable to give informed consent due to intoxication or altered mental status
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Feasibility of enrollment
Time Frame: at study enrollment
|
The investigators will assess the number of patients who were screened and enrolled at the study site
|
at study enrollment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Type of preventative services offered after a prior fall
Time Frame: at study enrollment
|
Participant will be asked what services they were provided after prior falls.
|
at study enrollment
|
Satisfaction with prior Emergency Department evaluations after a fall using a likert scale
Time Frame: at study enrollment
|
Participant will be asked about their satisfaction with prior fall assessments in the ED.
|
at study enrollment
|
Feedback on prior fall evaluations
Time Frame: at study enrollment
|
Participants will give free-text feedback on their perception of the quality of prior outpatient and inpatient fall care
|
at study enrollment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Elizabeth M Goldberg, MD, Rhode Island Hospital, Brown University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 14, 2017
Primary Completion (Actual)
May 30, 2017
Study Completion (Actual)
April 1, 2018
Study Registration Dates
First Submitted
March 2, 2017
First Submitted That Met QC Criteria
March 6, 2017
First Posted (Actual)
March 10, 2017
Study Record Updates
Last Update Posted (Actual)
September 27, 2021
Last Update Submitted That Met QC Criteria
September 20, 2021
Last Verified
September 1, 2021
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- UEMF0010
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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