Optometric Follow-up After Cataract Surgery

Queen's University Belfast

Status: Withdrawn

Conditions: Cataract; Age-related Cataract

Treatments: Procedure: Usual Care consultant follow up; Procedure: Intervention Group cataract follow up

Study type: Interventional

Funder types: Other

Identifiers

NCT04163926

B17/29

Details and patient eligibility

About

This study will investigate the effectiveness of an optometric follow up of cataract surgery versus an ophthalmic surgeon follow up. It will investigate patient satisfaction,safety and cost.

Full description

The study will be a mixed-methods study, including a randomized controlled trial in which participants are randomized after cataract surgery to follow up to be consultant led follow up or conducted by a trained optometrist 4-6 weeks following surgery. All participants will then return 6 months after surgery for an additional follow-up visit with an ophthalmologist other than the operating surgeon with patient healthcare satisfaction (main outcome), cost-effectiveness and safety outcomes being measured. A subset of patients and local clinicians will also take part in a one-time, individual, semi-structured interview.

This research will test an alternative model of aftercare for cataract surgeries, which may reduce patient waiting time and inconvenience. In turn, this could help improve patient satisfaction and reduce costs for both patients and the National Health Service (NHS).

Participants will be recruited by operating surgeons. The research will take place in the hospital/clinic/optometrists' offices.

Sex: All

Ages: 50+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients undergoing cataract surgery in 1st or 2nd eye for age-related cataract, in the Belfast Trust and Southern Trust
• Willing to participate and give informed consent.

Exclusion criteria

• Patients judged by operative surgeon to be of high risk of loss of visual acuity in the operative eye (e.g. end stage glaucoma etc.). Note that patients with ocular comorbidity and previous surgery will not be routinely excluded, nor will monocular patients.
• Patients that were not referred by an optometrist.

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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0 participants in 2 patient groups

Intervention group - Post op follow up by trained optometrist

Experimental group

Description:

Intervention group will have cataract follow up conducted by a trained optometrist 4-6 weeks after surgery in community clinic

Treatment:

Procedure: Intervention Group cataract follow up

Usual care group - Consultant led post op follow up

Active Comparator group

Description:

Follow-up at 4-6 weeks after surgery led by consultant ophthalmologist

Treatment:

Procedure: Usual Care consultant follow up