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Seeing to Learn in Sierra Leone

Seeing to Learn in Sierra Leone: Impact of Spectacle Correction on Children's Academic Performance and Mental Health Wellbeing

Status
Terminated
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06065631
Acronym
SLII
Enrollment
1821
Registered
2023-10-04
Start date
2023-10-25
Completion date
2025-01-31
Last updated
2026-01-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Refractive Errors

Keywords

Myopia, Hyperopia, Spectacle correction, Educational outcomes

Brief summary

The main objective of the Sierra Leone Sees to Learn (SL2) trial is to assess the educational impact of providing free eyeglasses to students aged 9-20 years with uncorrected refractive error in Sierra Leone. The procedures include baseline questionnaires and educational assessments to collect data on students and schools, and then the provision of free eyeglasses to students who have uncorrected (or undercorrected) refractive error (URE). The questionnaires and student assessments will take 1-2 hours. The duration of the study timeframe is one school year. The end-line questionnaires and student assessments will be administered at the end of the school year.

Detailed description

Objective: The main objective of the Sierra Leone Sees to Learn (SL2) trial is to assess the educational impact of providing free eyeglasses to students aged 9-20 years with uncorrected refractive error in Sierra Leone. Sample frame: Approximately 2400 children with uncorrected (or undercorrected) refractive error (URE) at 300 randomly-selected schools in Freetown and Bo City. A similar number of children from the same schools but without vision problems will also be included, at baseline only, to compare their basic demographic characteristics and daily activities to those of the children with URE. The sample size may vary depending on the percentage of children with URE obtained from screening a total of 40,000 children. All children with URE as specified in the enrolment criteria below will be part of the study. Design: Cluster-randomized control trial (cluster RCT), with schools as clusters. Randomization, interventions and balancing: All eligible children will be randomized by school to receive at the start of the school year either: free ready-made or custom eyeglasses (Intervention), or an eyeglasses prescription and letter to parents, with free eyeglasses at end-line (Control). The clusters (schools) will be stratified into groups based on the prevalence of refractive error and on the score on the baseline mathematics and reading exams. The division of the sample into schools in the two cities (Bo and Freetown) will be in the same proportion as the proportion of the number of public schools in those two cities. Power calculations (reading and math exams): Setting power = 0.8, statistical precision = 0.05, intracluster correlation = 0.2 (from 2019 Sierra Leone grade 8 learning assessment), 80 treated schools, 80 control schools, 15 students/school with uncorrected error, yields the following minimal detectable effect (MDE) sizes as a function of correlation between baseline and end-line tests: MDE Correlation of baseline and end-line tests 0.101 0.7 0.127 0.6 0.148 0.5 A nested focus-group study will explore children's, parents' and teachers' attitudes towards vision, student learning, and wearing of eyeglasses, in order to design a locally-tailored intervention to promote wearing of eyeglasses. Regression Framework: The investigators will estimate the effect of the program using a single difference cross-sectional ordinary least squares regression (OLS), and a difference-in-difference (DID) OLS regression that includes observations at both end-line and baseline. The investigators will report two types of effects: the intent-to-treat (ITT) effects and local average treatment effects (LATE), using treatment assignment as an instrumental variable for participation. Analysis will use the observed baseline characteristics as control variables and account for school-level variation through a fixed effect.

Interventions

DEVICEEyeglasses

Children with uncorrected/under-corrected refractive error will be provided with either ready made or custom eyeglasses based on their magnitude and types of refractive errors.

OTHERPrescription slip

Children with uncorrected/under-corrected refractive error will be provided with an eyeglasses prescription and letter to parents, but all of them will get eyeglasses at the end of the trial

Sponsors

University of Minnesota
Lead SponsorOTHER
Innovations for Poverty Action
CollaboratorOTHER
Peek Vision
CollaboratorUNKNOWN
Vision Action
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

Participants will be given either glasses or a prescription. Hence, they could not be masked. The Care Provider, in our case, screening and examination team will be providing either glasses or prescriptions to the participants. Hence, they could not masked. Investigators and Outcome assessor will only analyse the data at the end of the trial and they will not be

Intervention model description

All eligible children will be randomized by school to receive at the start of the school year either: free ready-made or custom eyeglasses (Intervention), or an eyeglasses prescription and letter to parents, with free eyeglasses at endline (Control). The clusters (schools) will be stratified into groups based on the prevalence of refractive error and on the score on the baseline mathematics and reading exams. The division of the sample into schools in the two cities (Bo and Freetown) will be in the same proportion as the proportion of the number of public schools in those two cities.

Eligibility

Sex/Gender
ALL
Age
9 Years to 20 Years
Healthy volunteers
No

Inclusion criteria

1. Presenting (with or without glasses) distance visual acuity of 6/12 or worse in the better-seeing eye; 2. Refractive error of at least 0.75 diopters (D) of myopia, 2.00 D of hyperopia or 1.00 D of astigmatism; 3. Visual acuity is correctable to 6/7.5 or better with eyeglasses.

Exclusion criteria

1\. Other ocular problems preventing visual acuity \> 6/12 in both eyes.

Design outcomes

Primary

MeasureTime frameDescription
Foundational mathematic and literacy skillsMonth 1 and 9 months after glasses are providedItem Response Theory to estimate a student's ability on a continuous scale and subsequently standardize students' scores on a continuous scale with respect to the control-group distribution at baseline (mean zero, standard deviation of one). Lower scores will indicate lower performance, and higher scores will indicate higher performance. A -1 would indicate a student's performance is 1 standard deviation below the mean of the control-group performance distribution at baseline. A zero would mean the student performed like the mean student in the control group at baseline.
AnxietyMonth 1 and 9 months after glasses are providedMeasured using Generalized Anxiety Disorder 2-item (GAD-2) questionnaire, the highest score is 8 and the lowest score is 2. Higher scores indicated more severe anxiety disorders.
ProsocialMonth 1 and 9 months after glasses are providedMeasured using Strengths \& Difficulties Questionnaire with the prosocial score ranges from 0 to 10 and higher scores indicate more prosocial behaviour.
Social and emotional problemsMonth 1 and 9 months after glasses are providedMeasured using Strengths \& Difficulties Questionnaire with the score ranges from 0 to 40. Higher scores indicate more social and emotional problems.

Secondary

MeasureTime frameDescription
Teacher-observed wearing of eyeglasses of childrenMonth 1 to Month 9 after glasses are providedProportion of children observed wear across all children at daily assessments
Self-reported wearing of eyeglasses complianceMonth 9 after glasses are providedProportion of children who reported to be wearing their eyeglasses 1. Not at all 2. Sometimes 3. Most of the time 4. All the time
Enumerator-observed wearing of eyeglassesAt Months 3, 6 and 9 after glasses are providedActual presence of spectacles on the child's face (rather than having glasses at school) at the time of an unannounced examination
Cost-effectiveness 1Through study completion, an average of 9 monthsTotal eyeglasses distribution cost (excluding study cost) per child receiving, and wearing, eyeglasses at endline
Cost-effectiveness 2Through study completion, an average of 9 monthsTotal eyeglasses distribution cost (excluding study cost) per 0.1 standard deviation test score gain
School attendanceDaily from Month 1 to Month 9Attendance data will be collected from attendance registry at school. This will be expressed in percentage. Lowest attendance being 0%, highest being 100%.

Countries

Sierra Leone

Contacts

PRINCIPAL_INVESTIGATORNathan Congdon, MD

Queen's University, Belfast

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026