ISRCTN75888393Completed未知
Feasibility and Acceptability of a New Clinical Pathway for the Identification of Non-responders to Glaucoma Eye Drops: The TRIAGE Study
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Cardiff University
- Enrollment
- 53
Study Overview
Brief Summary
2020 results in https://pubmed.ncbi.nlm.nih.gov/32139500/ (added 26/10/2020)
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •RQ1: CLINICAL OBSERVATIONS, SITUATED INTERVIEWS AND SURVEY
- •Observations and Situated Interviews:
- •1. Aged 18 years or over
- •2. Attending an outpatient glaucoma clinic
- •3. Diagnosed with either glaucoma, ocular hypertension, normal tension glaucoma or pseudo-exfoliative glaucoma
- •4. Cognitively able to participate in the study
- •5. Able to speak English or have access to an interpreter.
- •6. Healthcare professionals will be eligible for inclusion if they are providing care to patients fitting the inclusion criteria within either of the primary research sites.
- •1. Glaucoma specialist lead or nominated individual in a Welsh health board aside from Cwm Taf University Health Board and Cardiff and Vale University Health Board.
- •RQ2: SOP DEVELOPMENT AND FOCUS GROUPS ON STANDARD OPERATING PROCEDURE
- •SOP Development:
- •1. From one of the following stakeholder groups: nurses, doctors, optometrists, orthoptists, pharmacists, and glaucoma patients.
- •2. Aged 18 years or over
- •3. Must be cognitively able to participate
- •4. Able to speak English.
- •Focus Groups:
- •1. From one of the following stakeholder groups: glaucoma patient, lay carer of a glaucoma patient, doctor providing glaucoma care, pharmacist, optometrist, orthoptist, nurse providing glaucoma care, policy maker or NHS manager.
- •2. Aged 18 years or over
- •3. Must be cognitively able to participate
- •4. Able to speak English.
- •RQ3: COHORT FEASIBILITY STUDY
- •CMGC Cohort Feasibility Study:
- •1. Aged 18 years or over
- •2. Diagnosed with either primary open angle glaucoma, ocular hypertension, pseudo-exfoliative glaucoma, IOP equal to or greater than 21 mmHg, or normal tension glaucoma
- •3. Be on the point of being prescribed glaucoma eye drops.
- •4. Must be cognitively able to participate
- •5. Able to speak English or have access to an interpreter.
- •CMGC Staff Training:
- •1. Healthcare professionals are required to be working in one of the two ophthalmic research sites as either a doctor, nurse, orthoptist or optometrist.
- •RQ4: PATIENT / HEALTHCARE PROFESSIONAL INTERVIEWS AND OBSERVATION
- •Patient Interviews:
- •1. Adult patients aged 18 years or over
- •2. Diagnosed with either glaucoma, ocular hypertension, normal tension glaucoma or pseudo-exfoliative glaucoma
- •3. Cognitively able to participate in the study
- •4. Have either i) never participated in CMGC and whom are eye drop naïve, or ii) never participated in CMGC and who are established eye drop users, or iii) participated in CMGC and are up to 4 months post-CMGC.
- •Healthcare Professional Interviews:
- •1. Healthcare professional or member of the management team involved in the operation of the CMGC study.
- •Observation:
- •1. Glaucoma patient receiving the CMGC intervention (aged 18 years or over) OR
- •2. Healthcare professional or member of the clinical team involved in the operation of the CMGC study
Exclusion Criteria
- •RQ3: COHORT FEASIBILITY STUDY
- •CMGC Cohort Feasibility Study:
- •1. Ocular surgery in the last three months
- •2. Having a form of acute glaucoma
- •3. Already being prescribed and taking eye drops
- •4. Any other condition that may affect drop efficacy
Investigators
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