Lanzamiento Enero 2027

Ensayo controlado aleatorizado2026Vínculos de autores con la industriaAcceso abierto

Repeated low-level red-light therapy for improving asthenopic symptoms and accommodation in presbyopia

Song F, Zhao Z, Zhang J, Li J, Wu Y, Liu Y, Li P, Wang Y, Lai M, He M, Chen Y

Annals of medicine · 0 citas

Etiquetas de revisión

Vínculos de autores con la industria

Datos neutrales que nuestra revisión registró sobre cómo se hizo este estudio. Describen el método, nunca si nos gusta el resultado.

Cómo se estudió

Diseño
Ensayo controlado aleatorizado (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Marcadores de salud y funcionamiento

Quién lo pagó

Financiación
Financiación independiente
Universidad u hospital
Hong Kong Polytechnic University
Autores
Al menos un autor declara un vínculo económico con la industria
Subvenciones
Hong Kong Polytechnic University (P0046113)

Según 1 financiador declarado y la declaración de financiación del texto completo.

Publicación

Publicado
2026-04-28 · Ann Med · vol. 58 · número 1 · pág. 2663105
Editorial
Informa
Citado
0 citas · más que el 35% de estudios similares · 0.0× el promedio de su campo
Referencias
41 trabajos
Acceso
Acceso abierto (revista) · CC-BY
Áreas de investigación
Ophthalmology and Visual Impairment Studies · Spatial Neglect and Hemispheric Dysfunction · Ergonomics and Musculoskeletal Disorders
Palabras clave
Presbyopia, Blinding, Randomization, Accommodation, Randomized controlled trial, Adverse effect, Near vision, Refractive error
MeSH
humans, asthenopia, presbyopia, treatment outcome, double-blind method, visual acuity, accommodation, ocular, adult, middle aged, female, male, surveys and questionnaires, low-level light therapy, red light

11 autores

  • Fan Song🇭🇰Hong Kong Polytechnic University
  • Ziwei Zhao🇭🇰Hong Kong Polytechnic University
  • J Q Zhang🇨🇳Sun Yat-sen University
  • Jijing Li🇦🇺Vision Eye Institute
  • Yue Wu🇭🇰Hong Kong Polytechnic University
  • Ying Liu🇭🇰Hong Kong Polytechnic University
  • Pengju Li🇭🇰Hong Kong Polytechnic University
  • Yueye Wang🇭🇰Hong Kong Polytechnic University
  • Mengying Lai🇭🇰Hong Kong Polytechnic University
  • Mingguang He🇭🇰🇦🇺 · autor de correspondenciaHong Kong Polytechnic University; Vision Eye Institute
  • Yanxian Chen🇭🇰 · autor de correspondenciaHong Kong Polytechnic University

Resumen

El texto original del estudio, en el idioma en que se publicó.

Background

To assess the short-term effectiveness of repeated low-level red light (RLRL) therapy in relieving asthenopia and enhancing accommodation in presbyopia.

Methods

This randomized, parallel-group, double-masked clinical trial enrolled adults with presbyopia and self-reported asthenopia. Participants were allocated using computer-generated randomization and randomly assigned at a 1:1 ratio to RLRL or sham groups. Blinding included participants, examiners, assessors, and statisticians. The primary outcome was the change from baseline in the Computer Vision Syndrome Questionnaire (CVS-Q) score at day 31. Secondary outcomes were the change in accommodative amplitude (AA), Near Activity Visual Questionnaire (NAVQ) score, habitual near visual acuity, near-addition power, accommodative facility, positive and negative relative accommodation, binocular cross-cylinder response, and accommodative convergence-to-accommodation ratio. Continuous outcomes were analyzed using linear mixed-effects models.

Results

Sixty-four of 66 randomized participants (aged 41-62 years) completed the 1-month trial. At day 31, RLRL showed greater improvement than sham in CVS-Q score (adjusted mean difference, -1.75 points; 95% CI, -3.10 to -0.39), binocular AA (1.09 D; 95% CI, 0.37 to 1.82), and NAVQ score (-8.07 points; 95% CI, -14.17 to -1.97). The effect on AA was most pronounced in a subgroup of eyes with baseline amplitude >2.0 D (adjusted mean difference 1.33 D; 95% CI 0.32-2.34). Other measures did not differ between groups at each visit. No treatment-related adverse events were reported. Adherence was similar between groups (mean compliance: 98.2% vs 97.5%).

Conclusions

Short-term treatment with RLRL significantly reduced asthenopic symptoms and improved accommodative amplitude in individuals with presbyopia.Trial registration: NCT06745661 (registered December 8, 2024).

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial (CC BY).

Confianza de la comunidad

Cargando…

¿Cuánto confías en los hallazgos de este estudio?

0 · nada10 · totalmente

Comentarios

¿Algo está mal aquí?

Señala este estudio si su información, etiquetas o financiación parecen incorrectas. Un editor revisa cada señalamiento.

Información educativa sobre investigación publicada. No es consejo médico ni una recomendación para empezar o dejar nada.