PROSPERII: PROductivity Study of Presbyopia Elimination in Rural-dwellers II

Sponsor
Queen's University, Belfast (Other)
Overall Status
Recruiting
CT.gov ID
NCT04629820
Collaborator
VisionSpring (Other), University of Michigan (Other), Good Business Lab (Other), Zhongshan Ophthalmic Center, Sun Yat-sen University (Other), Clearly (Other)
500
1
2
24
20.8

Study Details

Study Description

Brief Summary

The investigators will conduct a randomized-controlled trial. The participants will be textile workers aged 30 years and above with uncorrected presbyopia who are employed by a single Indian garment manufacturer - employed by Shahi Exports Private Limited, Karnataka, India - at facilities equipped to measure individual productivity. PROSPER II will assess the impact of free reading glasses on productivity for workers in a textile factory.

Condition or Disease Intervention/Treatment Phase
  • Device: Spectacles
N/A

Detailed Description

Globally, 3 billion people do not have the eyeglasses they need to earn, learn, travel safely in traffic and participate in civic life. Among these, 1.1 billion people lack a simple pair of reading glasses to correct impaired near vision, called presbyopia. Presbyopia, the essentially universal decline in unaided near vision that occurs with aging, is the world's most common cause of vision impairment. Loss of accommodation (ability to change focus from distance to near) due to presbyopia can begin as early as age 30 years, commonly becomes functionally apparent by 40, and is essentially complete by 55, meaning that presbyopia is most common at the height of the working years.

Study Plan: This is a randomized trial designed to assess the impact of free spectacles on workplace productivity among Indian textile workers.

Research question: Will providing free glasses to presbyopic Indian textile workers increase work productivity?

Design: Investigator-masked, multi-center randomized controlled trial

Rationale: Although presbyopia is safely, effectively and inexpensively treated with glasses, rates of optical correction in LMICs are as low as 10%. The global productivity loss due to uncorrected presbyopia has been estimated to exceed US$25 billion, and presbyopia is shown to be associated with significant impairment in activities of daily living. Few trials have been published which address the question of whether healthcare interventions can improve work performance as well as workplace retention, especially among persons over the age of 40 in low and middle-income countries (LMICs). The largest reported effect sizes among such trials was the PROSPER trial, which showed that providing inexpensive near vision glasses increased the daily weight of tea picked among presbyopic, mostly-female Indian agricultural workers by more than 5 kg (21.6%) compared to those in the control group. Costs were low, over half of pickers aged >= 40 years met criteria to receive glasses, and wearing compliance reached nearly 90%. There is interest to understand if these results from the agricultural setting can be extended to other financially-important sectors.

Methods : The investigators will enrol 500 textile workers aged 30 years and above with uncorrected presbyopia who are employed by Shahi Exports Private Limited in Karnataka, India. Eligible participants will be randomly assigned to Intervention and Control Groups (1:1). Intervention group participants will receive free reading glasses within a week of undergoing a vision screening at the factory. Control group participants will receive reading glasses at the end of the assessment period (three months after vision screening).

The main outcome 3 month later will be work productivity; secondary outcomes are change in skill grade, change in monthly wage, participants' adherence with spectacle wear, self-assessed self-efficacy score and change of quality of life scores. The intervention cost-effectiveness will be studied.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
500 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
500 textile workers aged 30 years and above with uncorrected presbyopia will be randomized to receive free glasses within one week of undergoing vision assessment, or free glasses at the end of the study assessment (3 months after vision assessment).500 textile workers aged 30 years and above with uncorrected presbyopia will be randomized to receive free glasses within one week of undergoing vision assessment, or free glasses at the end of the study assessment (3 months after vision assessment).
Masking:
Double (Investigator, Outcomes Assessor)
Masking Description:
Study personnel assessing trial outcomes will be masked as to participants assignment, which will be simplified by the fact that there will be participants with and without glasses at both Intervention and Control. It is not ethical in this setting to provide Control participants with placebo treatment (glasses with zero power lenses), but participants will not be informed of either the overall design of the study or the explicit treatment intervention assignment.
Primary Purpose:
Treatment
Official Title:
Effects of Near Vision Spectacle Correction on Work Productivity Among Textile Factory Workers in India
Actual Study Start Date :
May 25, 2022
Anticipated Primary Completion Date :
May 24, 2024
Anticipated Study Completion Date :
May 24, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

Workers assigned to the intervention group will receive free spectacles of a design they select, based on the worker's measured refractive power and dispensed one week later at the factory by the study ophthalmic personnel.

Device: Spectacles
Intervention group workers receive free glasses within one week of undergoing vision assessment (September 2021). The assessment period will be three months
Other Names:
  • Near eyeglasses
  • Reading glasses
  • No Intervention: Control

    Workers assigned to the Control group will receive similar free glasses at the end of the study assessment (3 months).

    Outcome Measures

    Primary Outcome Measures

    1. Difference in change in mean efficiency between intervention and control group [Over the three month follow-up period from enrolment to study completion]

      Efficiency is calculated as the proportion of target production realized by a worker per unit time

    Secondary Outcome Measures

    1. Three-month change in skill grade [Between baseline and study end three months later]

      Skill grade ranges from A triple star (highest) to A double star, A star, A, B, and C + (lowest)

    2. Change in monthly wage [Between baseline and study end three months later]

      Monthly wage

    3. Adherence with spectacle wear [Between baseline and study end three months later]

      measured weekly by supervisor's unannounced direct observations of the presence of spectacles worn on the participant's face.

    4. Group difference in three-month change in self-assessed self-efficacy scores [Between baseline and conclusion of the study three months later]

      Self-assessed self-efficacy scores measured using the Cantril's Ladder, with the best possible score being a 10, and the worst being a 0

    5. Group difference in three-month change of quality of life scores [Between baseline and conclusion of the study three months later]

      Quality of life scores measured using the THRIVE Near Vision Quality of Life tool, a Likert Scale ranging from 1 (least affected) to 5 (worst affected).

    6. Cost effectiveness [Between baseline and study end three months later]

      Full programme costs per individual identified and corrected with presbyopia. Programme costs include costs incurred in screening test, glasses / replacement and direct/indirect costs for facilitating work-based site. Effectiveness will be measured using work productivity

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    30 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Aged 30 years and above

    • Distance visual acuity >= 6/12 in both eyes

    • Presence of presbyopia, defined as the inability, correctable with reading glasses, to read the N8 line using both eyes together, on a tumbling near vision chart at a distance of 40cm

    • Employed at the factory for >=3months in the sewing department

    Exclusion Criteria:
    • Current ownership of reading or distance glasses (regardless of accuracy)

    • Obvious evidence of ocular disease in either eye detected during the eye examination, or history of such disease based on self-report

    • Low likelihood of completing follow-up in the study due to current plans to move out of the area or leave employment at Shahi during the follow-up period

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Good Business Lab Bengaluru Karnataka India 560102

    Sponsors and Collaborators

    • Queen's University, Belfast
    • VisionSpring
    • University of Michigan
    • Good Business Lab
    • Zhongshan Ophthalmic Center, Sun Yat-sen University
    • Clearly

    Investigators

    • Principal Investigator: Nathan G Congdon, MD, MPH, Queen's University, Belfast

    Study Documents (Full-Text)

    More Information

    Publications

    None provided.
    Responsible Party:
    Nathan Congdon, Professor, Queen's University, Belfast
    ClinicalTrials.gov Identifier:
    NCT04629820
    Other Study ID Numbers:
    • MHLS 20_82
    First Posted:
    Nov 16, 2020
    Last Update Posted:
    May 26, 2022
    Last Verified:
    May 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Nathan Congdon, Professor, Queen's University, Belfast
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 26, 2022