Quality-Assured Follow-up of Quiescent Neovascular Age -Related maculaR dEgeneration by Non-medical Practitioners

NCT ID: NCT03893474

Last Updated: 2021-09-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

742 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-09-30

Study Completion Date

2022-11-30

Brief Summary

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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

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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.

Conditions

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AMD

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Control Arm

All investigations are the same in both arms, but patients within this arm will be seen in the hospital as per standard practice.

Group Type OTHER

OCT

Intervention Type DIAGNOSTIC_TEST

Optical Coherence Tomography of study eye.

Visual Acuity

Intervention Type DIAGNOSTIC_TEST

Visual acuity measured by ETDRS

Study Arm

All investigations are the same in both arms, but patients within this arm will be seen in a community optometrist practice.

Group Type OTHER

OCT

Intervention Type DIAGNOSTIC_TEST

Optical Coherence Tomography of study eye.

Visual Acuity

Intervention Type DIAGNOSTIC_TEST

Visual acuity measured by ETDRS

Interventions

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OCT

Optical Coherence Tomography of study eye.

Intervention Type DIAGNOSTIC_TEST

Visual Acuity

Visual acuity measured by ETDRS

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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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).
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute for Health Research, United Kingdom

OTHER_GOV

Sponsor Role collaborator

Newcastle University

OTHER

Sponsor Role collaborator

Cardiff University

OTHER

Sponsor Role collaborator

City, University of London

OTHER

Sponsor Role collaborator

King's College London

OTHER

Sponsor Role collaborator

Manchester University NHS Foundation Trust

OTHER_GOV

Sponsor Role collaborator

University Hospitals Bristol and Weston NHS Foundation Trust

OTHER

Sponsor Role collaborator

York Teaching Hospitals NHS Foundation Trust

OTHER

Sponsor Role collaborator

Leeds Teaching Hospital NHS Foundation Trust

UNKNOWN

Sponsor Role collaborator

Bradford Teaching Hospitals NHS Foundation Trust

OTHER_GOV

Sponsor Role collaborator

University College, London

OTHER

Sponsor Role collaborator

Moorfields Eye Hospital NHS Foundation Trust

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Konstantinos Balaskas

Role: PRINCIPAL_INVESTIGATOR

Moorfields Eye Hospital NHS Foundation Trust

Locations

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Moorfields Eye Hospital NHS Foundation Trust, 162 City Road

London, , United Kingdom

Site Status RECRUITING

Countries

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United Kingdom

Facility Contacts

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Lauren Leitch-Devlin

Role: primary

020 7253 3411

References

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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.

Reference Type DERIVED
PMID: 33980536 (View on PubMed)

Other Identifiers

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BALK1005

Identifier Type: -

Identifier Source: org_study_id

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