SynthesisThe Cochrane database of systematic reviews2025
Multifaceted behavioral interventions to improve topical glaucoma therapy adherence in adults.
Synthesis in The Cochrane database of systematic reviews, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
3 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Multifaceted behavioral interventions to improve topical glaucoma therapy adherence in adults.The Cochrane database of systematic reviews · 2025Pooled it
- Development and Pilot Testing of a Mobile App Psychosocial Intervention for Psychological Distress in Individuals with Glaucoma.medRxiv : the preprint server for health sciences · 2026Article
- A Qualitative Study of Factors Affecting Medication Adherence in Patients with Open-Angle Glaucoma.Clinical ophthalmology (Auckland, N.Z.) · 2026Article
Corrections and comments
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
rationaleGlaucoma is a leading cause of vision loss and blindness, characterized by optic nerve damage and commonly by increased intraocular pressure (IOP). Topical medical therapy is the most common first-line treatment option, yet adherence to these medications is notably low. Improving medication adherence is critical for managing glaucoma effectively.
objectivesTo assess the impact of two or more behavioral interventions (i.e. multifaceted interventions) on topical glaucoma therapy adherence in people utilizing IOP-lowering therapy for at least three months for treating ocular hypertension or glaucoma. SEARCH
methodsWe searched four electronic databases (CENTRAL, MEDLINE, Embase, LILACS), two clinical trial registries, and checked references. The latest search date was 31 May 2024. ELIGIBILITY CRITERIA: We included randomized controlled trials (RCTs) evaluating multifaceted behavioral interventions (≥ 3 months) for topical glaucoma therapy adherence compared with standard care in adults with glaucoma or ocular hypertension. OUTCOMES: Outcomes were change in adherence to topical IOP-lowering medications, change in IOP, optical coherence tomography (OCT) stability, visual field (VF) stability, proportion of participants with disease stability, change in quality of life scores, and adverse events. The time point for these measurements was three months or longer follow-up. We extracted any information related to equity and social determinants of health, and their potential influence on the administration of or outcomes from the interventions. RISK OF BIAS: We assessed the risk of bias for all outcomes reported in the summary of findings tables using the Cochrane risk of bias 2 (RoB 2) tool, except for outcomes where no data were available. SYNTHESIS
methodsWhere possible, we synthesized results for outcomes using random-effects meta-analysis of risk ratios (RRs) for dichotomous outcomes, and mean difference (MD) or standardized mean difference (SMD) for continuous outcomes. Where meta-analysis was not possible due to the available data, we synthesized the results qualitatively following Cochrane-recommended approaches; including summarizing effect estimates and vote counting, accompanied by forest plots to show estimates without meta-analyses and harvest plots. We used the GRADE approach to assess the certainty of the evidence for prespecified outcomes. INCLUDED STUDIES: We included 17 RCTs that enrolled 4536 participants, ranging from 64 to 1800 per study. The mean age of participants ranged from 42 to 76 years. Studies were conducted across North America, Europe, and Asia, with most in the USA (47%). Among 12 studies reporting race and ethnicity, most participants were White (62%), followed by Black (26%), Asian (7%), Hispanic (1%), and others (3%). Follow-up periods ranged from 3 to 24 months. All but one study received financial support from multiple sources. We assessed the risk of bias in 25 outcome measures across 17 studies. We judged one study to be at low risk of bias for both adherence to topical IOP-lowering medications and IOP measures. Four studies reported both outcomes and overall were judged to have some bias concerns, and we judged three studies to have some bias concerns for only adherence. Two studies reported both outcomes with high risk of bias, and another study had a high overall risk of bias for adherence and some concerns for IOP. The remaining nine studies reported adherence only, and we judged these as having some concerns (three studies) or high risk (six studies) of overall bias. SYNTHESIS OF
resultsIn general, evidence on the effect of multifaceted interventions in improving glaucoma-related outcomes was inconsistent. We conducted an overall meta-analysis of adherent participants that included all comparisons and related subgroups, suggesting any multifaceted intervention may increase the proportion of adherent participants over any control, but the evidence is very uncertain (RR 1.18, 95% confidence interval (CI) 1.01 to 1.38; 8 studies, 2184 participants; I AUTHORS'
conclusionsBased on very low- and low-certainty evidence identified in this review, it is unclear if multifaceted behavioral interventions have a beneficial effect on patient adherence to topical IOP-lowering medications and IOP in people with ocular hypertension or glaucoma. In most cases, we were unable to conduct meta-analysis due to the diversity of interventions, varying outcome definitions, and inconsistent reporting across studies. Future research would benefit from the adoption of standardized measurements and reporting methods for adherence to medication and clinical outcomes on disease stability, while taking social determinants into account.
fundingCochrane Eyes and Vision US Project is supported by grant UG1EY020522, National Eye Institute, National Institutes of Health. REGISTRATION: Protocol available via doi.org/10.1002/14651858.CD015788.
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