Quality-Assured Follow-up of Quiescent Neovascular Age -Related maculaR dEgeneration by Non-medical Practitioners (FENETRE)
Primary Purpose
AMD
Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
OCT
Visual Acuity
Sponsored by
About this trial
This is an interventional other trial for AMD focused on measuring AMD, nAMD
Eligibility Criteria
Inclusion Criteria:
- Participants receiving treatment in nAMD injection clinics, who have reached the agreed definition of disease quiescence
- Informed consent
- Aged > 55 years
- Ability to perform study specific procedures
Exclusion Criteria:
- Significant media opacities (cataract, vitreous opacities) that would not allow good quality fundus imaging.
- Diabetic retinopathy of severity worse than mild non-proliferative stage and with any degree of diabetic maculopathy
- History of other causes of Choroidal Neovascularisation (myopic, angioid streaks, inflammatory, retinal dystrophies, secondary to Central Serous Chorioretinopathy, idiopathic).
Sites / Locations
- Moorfields Eye Hospital NHS Foundation Trust, 162 City RoadRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
Control Arm
Study Arm
Arm Description
All investigations are the same in both arms, but patients within this arm will be seen in the hospital as per standard practice.
All investigations are the same in both arms, but patients within this arm will be seen in a community optometrist practice.
Outcomes
Primary Outcome Measures
The proportion of Participants who reactivate within 12 months of randomisation but are not identified as having re-activated (false negatives).
The proportion of Participants who reactivate within 12 months of randomisation but are not identified as having re-activated (false negatives).
Primary economic outcome: Incremental cost per quality adjusted life year (QALY) gained over the estimated patient lifetime estimated from an economic model informed by trial data.
Primary economic outcome: Incremental cost per quality adjusted life year (QALY) gained over the estimated patient lifetime estimated from an economic model informed by trial data.
Secondary Outcome Measures
Diagnostic accuracy of the intervention (community optometry follow up of QnAMD) against the reference standard (rate of false negatives and false positives)
Diagnostic accuracy of the intervention (community optometry follow up of QnAMD) against the reference standard (rate of false negatives and false positives)
Rate of over-referral (i.e. Reference Standard is quiescent but classification is 'reactivated' or 'suspicious')
Rate of over-referral (i.e. Reference Standard is quiescent but classification is 'reactivated' or 'suspicious')
Mean change in visual acuity (measured with habitual correction and pinhole) for in the Participants intervention and control groups
Mean change in visual acuity (measured with habitual correction and pinhole) for in the Participants intervention and control groups
Rate of 'suspicious' lesion classification in community care
Rate of 'suspicious' lesion classification in community care
Rate of patient non-attendance and loss to follow up in secondary and primary care
Rate of patient non-attendance and loss to follow up in secondary and primary care
Use of health services and patient costs collected via eCRF and participant completed questionnaires
Use of health services and patient costs collected via eCRF and participant completed questionnaires
Costs of interventions and subsequent care to the NHS modelled over the estimated lifetime
Costs of interventions and subsequent care to the NHS modelled over the estimated lifetime
Modelled estimates of visual impairment and QALYs based on responses to the EQ-5D-5L.
Modelled estimates of visual impairment and QALYs based on responses to the EQ-5D-5L
Full Information
NCT ID
NCT03893474
First Posted
March 26, 2019
Last Updated
September 16, 2021
Sponsor
Moorfields Eye Hospital NHS Foundation Trust
Collaborators
National Institute for Health Research, United Kingdom, Newcastle University, Cardiff University, City, University of London, King's College London, Manchester University NHS Foundation Trust, University Hospitals Bristol and Weston NHS Foundation Trust, York Teaching Hospitals NHS Foundation Trust, Leeds Teaching Hospital NHS Foundation Trust, Bradford Teaching Hospitals NHS Foundation Trust, University College, London
1. Study Identification
Unique Protocol Identification Number
NCT03893474
Brief Title
Quality-Assured Follow-up of Quiescent Neovascular Age -Related maculaR dEgeneration by Non-medical Practitioners
Acronym
FENETRE
Official Title
Quality-Assured Follow-up of Quiescent Neovascular Age -Related maculaR dEgeneration by Non-medical Practitioners: a Randomised Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
September 2021
Overall Recruitment Status
Unknown status
Study Start Date
September 30, 2019 (Actual)
Primary Completion Date
May 2022 (Anticipated)
Study Completion Date
November 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Moorfields Eye Hospital NHS Foundation Trust
Collaborators
National Institute for Health Research, United Kingdom, Newcastle University, Cardiff University, City, University of London, King's College London, Manchester University NHS Foundation Trust, University Hospitals Bristol and Weston NHS Foundation Trust, York Teaching Hospitals NHS Foundation Trust, Leeds Teaching Hospital NHS Foundation Trust, Bradford Teaching Hospitals NHS Foundation Trust, University College, London
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is a prospective, randomised, multi-site clinical trial testing the non-inferiority of community optometry follow-up of participants with QnAMD over 12 months
Detailed Description
Neovascular Age-Related Macular Degeneration (nAMD) is a common vision threatening condition affecting mainly patients over the age of 65. At some point during follow-up the disease becomes inactive in many cases and does not need more injections. The risk of a flare-up is high, however, and patients need to continue to be seen every month for a significant period of time.
Hospital-based eye clinics are struggling to cope with current and expected workload for assessing and treating patients with nAMD. Transferring care of these patients to the community closer to home would ease the workload for hospital based clinics and offer a better experience of care to patients.
This study will recruit 742 patients with nAMD who have reached this inactive phase of the disease. Half of the patients that want to take part will continue to have their follow-up appointments in the hospital eye clinics as usual. The other half, chosen by chance, will have follow-up visits every month in a community optometrist practice by trained optometrists. The research team will provide the training for community optometrists.
The study will seek to show that the community based care is no less safe than hospital-based care.
The study will also check what is the impact of this different way of offering care on the NHS budget and how the patients and practitioners perceive this. The study will involve several hospital eye clinics across the country and several community optometrist practices. Meetings will also be held with patients to discuss their priorities and needs when looking at how to set up the community based eye clinics.
During meetings with patients in preparation for this research, they felt positively about the possibility to receive care closer to home.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
AMD
Keywords
AMD, nAMD
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
742 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Control Arm
Arm Type
Other
Arm Description
All investigations are the same in both arms, but patients within this arm will be seen in the hospital as per standard practice.
Arm Title
Study Arm
Arm Type
Other
Arm Description
All investigations are the same in both arms, but patients within this arm will be seen in a community optometrist practice.
Intervention Type
Diagnostic Test
Intervention Name(s)
OCT
Intervention Description
Optical Coherence Tomography of study eye.
Intervention Type
Diagnostic Test
Intervention Name(s)
Visual Acuity
Intervention Description
Visual acuity measured by ETDRS
Primary Outcome Measure Information:
Title
The proportion of Participants who reactivate within 12 months of randomisation but are not identified as having re-activated (false negatives).
Description
The proportion of Participants who reactivate within 12 months of randomisation but are not identified as having re-activated (false negatives).
Time Frame
12 months
Title
Primary economic outcome: Incremental cost per quality adjusted life year (QALY) gained over the estimated patient lifetime estimated from an economic model informed by trial data.
Description
Primary economic outcome: Incremental cost per quality adjusted life year (QALY) gained over the estimated patient lifetime estimated from an economic model informed by trial data.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Diagnostic accuracy of the intervention (community optometry follow up of QnAMD) against the reference standard (rate of false negatives and false positives)
Description
Diagnostic accuracy of the intervention (community optometry follow up of QnAMD) against the reference standard (rate of false negatives and false positives)
Time Frame
12 months
Title
Rate of over-referral (i.e. Reference Standard is quiescent but classification is 'reactivated' or 'suspicious')
Description
Rate of over-referral (i.e. Reference Standard is quiescent but classification is 'reactivated' or 'suspicious')
Time Frame
12 months
Title
Mean change in visual acuity (measured with habitual correction and pinhole) for in the Participants intervention and control groups
Description
Mean change in visual acuity (measured with habitual correction and pinhole) for in the Participants intervention and control groups
Time Frame
12 months
Title
Rate of 'suspicious' lesion classification in community care
Description
Rate of 'suspicious' lesion classification in community care
Time Frame
12 months
Title
Rate of patient non-attendance and loss to follow up in secondary and primary care
Description
Rate of patient non-attendance and loss to follow up in secondary and primary care
Time Frame
12 months
Title
Use of health services and patient costs collected via eCRF and participant completed questionnaires
Description
Use of health services and patient costs collected via eCRF and participant completed questionnaires
Time Frame
12 months
Title
Costs of interventions and subsequent care to the NHS modelled over the estimated lifetime
Description
Costs of interventions and subsequent care to the NHS modelled over the estimated lifetime
Time Frame
12 months
Title
Modelled estimates of visual impairment and QALYs based on responses to the EQ-5D-5L.
Description
Modelled estimates of visual impairment and QALYs based on responses to the EQ-5D-5L
Time Frame
12 months
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Participants receiving treatment in nAMD injection clinics, who have reached the agreed definition of disease quiescence
Informed consent
Aged > 55 years
Ability to perform study specific procedures
Exclusion Criteria:
Significant media opacities (cataract, vitreous opacities) that would not allow good quality fundus imaging.
Diabetic retinopathy of severity worse than mild non-proliferative stage and with any degree of diabetic maculopathy
History of other causes of Choroidal Neovascularisation (myopic, angioid streaks, inflammatory, retinal dystrophies, secondary to Central Serous Chorioretinopathy, idiopathic).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Konstantinos Balaskas
Organizational Affiliation
Moorfields Eye Hospital NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Moorfields Eye Hospital NHS Foundation Trust, 162 City Road
City
London
ZIP/Postal Code
EC1V 2PD
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lauren Leitch-Devlin
Phone
020 7253 3411
Email
moorfields.resadmin@nhs.net
First Name & Middle Initial & Last Name & Degree
Konstantinos Balaskas
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
IPD will not be shared.
Citations:
PubMed Identifier
33980536
Citation
Learoyd AE, Tufail A, Bunce C, Keane PA, Kernohan A, Robinson E, Jaber A, Sadiq S, Harper R, Lawrenson J, Vale L, Waterman H, Douiri A, Balaskas K; FENETRE study group. FENETRE study: quality-assured follow-up of quiescent neovascular age-related macular degeneration by non-medical practitioners: study protocol and statistical analysis plan for a randomised controlled trial. BMJ Open. 2021 May 11;11(5):e049411. doi: 10.1136/bmjopen-2021-049411.
Results Reference
derived
Learn more about this trial
Quality-Assured Follow-up of Quiescent Neovascular Age -Related maculaR dEgeneration by Non-medical Practitioners
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