Actively Recruiting

Age: 4Years +
All Genders
Healthy Volunteers
NCT05941182

Co-designing and Evaluating a Real-world Implementation Model for Remote Consultation with Vision Self-testing.

Led by Cambridge University Hospitals NHS Foundation Trust · Updated on 2025-02-12

200

Participants Needed

2

Research Sites

126 weeks

Total Duration

On this page

Sponsors

C

Cambridge University Hospitals NHS Foundation Trust

Lead Sponsor

M

Manchester University NHS Foundation Trust

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study aims to involve the public, patients and National Health Service (NHS) staff in co-designing a scalable, inclusive and sustainable implementation model for ophthalmic remote consultation with vision self-testing (the intervention). The main study questions are: What are the barriers to uptake of the intervention and how can these be mitigated by the design of the implementation model. How do implementation outcome measures compare before and after real world application of the model.

CONDITIONS

Official Title

Co-designing and Evaluating a Real-world Implementation Model for Remote Consultation with Vision Self-testing.

Who Can Participate

Age: 4Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 4 years and older scheduled by their clinician for a follow up remote eye clinic consultation following an initial face-to face consultation.
Not Eligible

You will not qualify if you...

  • Patients refusing remote consultation or converted to a face-to-face appointment following scheduling.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Cambridge University Hospital NHS Trust

Cambridge, Cambridgeshire, United Kingdom, CB22 4XU

Actively Recruiting

2

Manchester University Hospitals NHS Trust

Manchester, United Kingdom

Actively Recruiting

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Research Team

L

Louise Allen

CONTACT

M

Mahmoud Hassan

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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