- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06645080
Vision Screening in Hospitals for Older Adults Following a Fall
Vision Screening in Hospitals for Older Adults Following a Fall: an Intervention Development Study
Aims
This study aims to improve the way vision is checked and sight loss treated in older adults (65 years or older), who attend hospital following a fall.
Background
Falling is common in older adults. As the number of older people grows, the number of falls is expected to increase as well. Falling can affect a person's life in several ways: it can lead to pain, injuries, difficulty doing normal daily activities, weaker muscles, feeling isolated, losing independence and confidence, living in fear of falling, depression, difficulty in recovering from illnesses, developing other health problems more easily and a higher risk of death. Falls are a major health problem for the public and the United Kingdom (UK) spends more than £2 billion per year on caring for older adults who fall.
Problems with eyesight are also more common in older age and can have a similar effect on a person's independence, happiness and almost doubles their chances of falling. Sight loss in older age that is linked to falling is often treatable.
UK guidelines have been made to help prevent falls. These guidelines recommend checking for and treating sight loss in all older adults who attend hospital following a fall. However, this is only being done in a small number of hospitals. The reasons for this need to be investigated, in order to encourage and make it easier for health professionals to follow these guidelines.
Research has also shown that older adults, may be less likely to get their eyes tested regularly and attend hospital eye appointments. There are many reasons for this and vision screening whilst the patient is already receiving care in hospital, may be a good opportunity to address these issues. The views of the public are important for developing screening services that they understand and meets their needs. This study will gather the views of older people and their carers on hospital vision screening after a fall and the importance of looking after their eyes.
This study aims to improve the way vision is checked in older adults who attend hospital following a fall. This will help to identify and treat sight loss that may contribute to repeated falling. The study will combine the views of older adults and health professionals, to ensure that changes made meet patients' needs and are sustainable.
Design and methods
This study will have three parts:
- Focus groups asking health professionals about checking vision in patients who have fallen.
- Focus groups asking patients who have fallen and their carers about looking after their eyes.
- Development of a way of checking vision and treating sight loss in older adults who attend hospital following a fall.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
England
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Nottingham, England, United Kingdom, NG7 2UH
- Nottingham University Hospitals Nhs Trust
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Part one- Focus group study (with healthcare professionals):
Members of the acute multidisciplinary team who care for falls patients at Nottingham University Hospitals NHS Trust (NUHT) will be recruited.
Part two- Focus group study (with service users/ carers):
Current patients of NUHT or others recruited from the public, aged 65 or over who have had a fall. Carers of people aged 65 or over who have had a fall.
Part three- Intervention development using Delphi study:
Professionals with relevant knowledge and experience of falls assessments and management in hospitals for older people or the assessment and management of impaired vision in older people.
Description
Inclusion Criteria:
Part one- Focus group study (with healthcare professionals):
- Aged 18 years or above
- Health professionals at NUHT
- Must be involved in falls assessments/ management/ care of older falls patients as part of current/ previous role at NUHT.
Part two- Focus group study (with service users/ carers):
- Adults ≥65 years
- Had at least 1 fall requiring attendance at an emergency department
- Carers of adults ≥65 who have had at least 1 fall requiring attendance at an emergency department
Part three- Intervention development using Delphi study:
- Aged 18 years or above
- Knowledge and experience of falls assessments and management in hospitals for older people
- Experience of the assessment and management of impaired vision in older people
Exclusion Criteria:
- Those who are unable to give voluntary informed consent.
- Those who have not sought secondary care following a fall.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Focus Group participants (health professionals)
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90 minute focus group or 60 minute interview participation
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Focus group participants (service users/ carers)
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90 minute focus group or 60 minute interview participation
|
|
Delphi study participants
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Participation in a modified two-round Delphi technique.
Optional third round in the event of insufficient agreement in the second round.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage agreement on Delphi survey components
Time Frame: Within 2 weeks of all Delphi round responses collected.
|
After each complete Delphi round, the percentage agreement of responses for each survey component will be calculated to help decide upon the subsequent Delphi survey items to be included.
Or, if in the case of the final survey round, to help decide if a further round is required in the event of disagreement.
|
Within 2 weeks of all Delphi round responses collected.
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 24056
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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