With or Without Compliance Aids: A Patient-Reported Outcomes Study

  • Research type

    Research Study

  • Full title

    With or Without Compliance Aids: A Patient-Reported Outcomes Study

  • IRAS ID

    357794

  • Contact name

    Rana Khalil

  • Contact email

    rana.khalil@nhs.scot

  • Sponsor organisation

    NHS Greater Glasgow & Clyde

  • Duration of Study in the UK

    0 years, 5 months, 31 days

  • Research summary

    Ophthalmic drugs are most commonly delivered in the form of eye drops. Despite
    advances in drug development, poor drop technique and medication
    non-adherence are usually the causes of treatment failure. Contributing factors include educational, social and physical barriers. Perfect drop administration is defined as the ability to instil a single drop on the first attempt, without touching the eye or lids. Recent studies suggest significant variability in good technique, even between individuals who are properly educated on drop use.

    It is well recognised that patients with any form of visual impairment struggle with drop application, due to difficulty centring the bottle over the eye, accidentally touching the eye, too much blinking, and reluctance to admit difficulties to medical professionals. Physical barriers include difficulty holding or squeezing the bottle.

    To date, only one study has directly compared the safety and efficacy of compliance aids (Autodrop® and Opticare®) to regular bottle use. In Scotland, some of these devices are available free of charge on prescription, although options are limited, and they do not fit all bottles. A more versatile recent product, EziDrops® (EziDrops Ltd, Watford, United Kingdom), fits all standard bottles with a nozzle and prevents involuntary blinking during drop delivery. Although it is not available on prescription, it is the cheapest aid to purchase privately (RRP £7.99) and has the potential to address the aforementioned problems. If successful, this may improve patient experience of drop delivery, and promote treatment adherence. We propose the first prospective patient-reported outcomes study comparing the user friendliness of the EziDrops® device with traditional eye drop bottles. The primary outcome measures will include subjective evaluation of drop technique, patient-reported confidence level and satisfaction with administration with and without the aid, and personal preference to either method using Likert scales.

  • REC name

    West of Scotland REC 5

  • REC reference

    25/WS/0110

  • Date of REC Opinion

    18 Jul 2025

  • REC opinion

    Favourable Opinion