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Search / Trial NCT03228199

PROductivity Study of Presbyopia Elimination in Rural-dwellers (PROSPER)

Launched by CONGDON NATHAN · Jul 19, 2017

Trial Information

Current as of May 21, 2025

Completed

Keywords

Randomised Control Trial Productivity Agricultural Workers India Vision Correction

ClinConnect Summary

Main research question being addressed: To establish, using a randomized, controlled design, the impact of near eyesight correction on the productivity of presbyopic agricultural workers in India, as measured by weight of tea picked.

Primary outcomes to be measured: Change in mean daily weight of tea picked per worker during a 12 weeks period after randomisation compared to a 4 weeks baseline period prior to randomisation. (See details below under Main Outcome.)

I. Background: Importance of research topic, Particular Features of setting Uncorrected presbyopia is an expensive problem for t...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Employee of APPL for 1 year
  • Aged \>= 40 years
  • Habitual near visual acuity of \>= 0.8M (\<=6/12) at 40cm in both eyes, correctable to \<=0.5M (\>=6/7.5) in both eyes with near glasses
  • Uncorrected distance vision \>= 6/7.5 in the better-seeing eye
  • The participant worked and has data available on weight of tea picked for \>=10 days in the previous 4 weeks (This will largely exclude men in this setting).
  • Ability to give informed consent
  • Exclusion Criteria:
  • Eye disease detected on baseline eye exam
  • Current ownership of near correction capable of improving near visual acuity to \<= 0.8M (\>= 6/12) in either eye
  • Unlikely to complete follow-up due to unsatisfactory work performance, plans to move out of the area, etc.
  • Need for distance correction to achieve distance vision of \>= 6/7.5 in the better-seeing eye.
  • Inability to achieve best-corrected visual acuity with spherical power glasses only (that is: need for astigmatic correction to achieve best-corrected near visual acuity)
  • Persons with eye problems detected on the examination will be referred for definitive care at local facilities, and distance refractive errors will be corrected with free bifocals for those with uncorrected VA \< 6/12 in the better-seeing eye.

About Congdon Nathan

Congdon Nathan is a leading clinical trial sponsor dedicated to advancing medical research through innovative study design and execution. With a focus on enhancing patient outcomes, the organization collaborates with healthcare professionals, researchers, and regulatory bodies to ensure the highest standards of safety and efficacy in clinical trials. By leveraging cutting-edge technology and data analytics, Congdon Nathan aims to streamline the clinical trial process, expedite drug development, and ultimately contribute to the creation of effective therapies in various therapeutic areas. Their commitment to ethical practices and patient-centered research underscores their role as a trusted partner in the pharmaceutical and biotechnology industries.

Locations

Tezpur, Assam, India

Patients applied

0 patients applied

Trial Officials

Nathan Congdon

Principal Investigator

Queen's University, Belfast

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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