- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07350408
Mapping Post-falls Organisational Processes in Care Homes (Post-falls)
April 24, 2026 updated by: Nottingham University Hospitals NHS Trust
Mapping Post-falls Management Organisational Processes for Older People Who Fall in Care Homes in England
The aim of this study is to map post-falls management organisational processes for older people in care homes.
The main question to answer is 'What post-falls management organisational processes are used for older people in care homes?' Participants (care home and healthcare staff) will complete a one off online national survey about policies and processes relating to falls management in their organisation.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
234
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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Nottinghamshire
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Nottingham, Nottinghamshire, United Kingdom, NG7 2UH
- Nottingham University Hospital NHS Trust
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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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Care home staff in any role or healthcare staff in any role working in a primary, community, emergency and acute settings in England, with experience of supporting older people immediately after a fall in a care home as part of their role
Description
Inclusion Criteria:
- Care home staff in any role or healthcare staff in any role working in a primary, community, emergency and acute settings
- Work in a care home or healthcare setting in England
- Has any previous experience in supporting older people immediately after a fall in a care home as part of their role
- Aged 16 years or over
Exclusion Criteria:
- Care home and healthcare staff working outside of England
- Staff working outside of stated settings
- No experience in supporting older people immediately after a fall in a care home as part of their role
- Under 16 years of age
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
post-falls practices for older people in care homes
Time Frame: Baseline only
|
The survey collects information about current policies and procedures being used to manage falls in care homes.
This is a one off cross-sectional survey to collect this information at a single time point.
|
Baseline only
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
November 12, 2025
Primary Completion (Actual)
February 28, 2026
Study Completion (Actual)
February 28, 2026
Study Registration Dates
First Submitted
December 11, 2025
First Submitted That Met QC Criteria
January 9, 2026
First Posted (Actual)
January 20, 2026
Study Record Updates
Last Update Posted (Actual)
April 30, 2026
Last Update Submitted That Met QC Criteria
April 24, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- 25HC001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
The anonymised Excel file containing survey responses will be made available upon request, for supporting further research and ensuring transparency, by contacting the CI after the results have been published.
Sharing the file will require sponsor approval.
The file will not contain identifiable information.
The spreadsheet will be sent securely from an NHS.net email address.
There will be no geographical restrictions.
Sharing research data will be in line with the NIHR's commitment to open access of research outputs
IPD Sharing Time Frame
After publication
IPD Sharing Access Criteria
For research purposes Sponsor approval required No geographical restrictions
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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