Effect of Presbyopia Correction on Livelihood and Repayment Among Solar Customers in Western Region, Kenya

Aim:

To identify the impact on SHS and mobile phone use, repayment behaviour and income, of providing near vision glasses (NVGs) to customers with near vision impairment (NVI).

Primary objective:

● To determine the effect of presbyopia correction via NVGs, on SHS and mobile phone repayment behaviour:

* The proportion of total payments made on time * Percentage of expected revenue collected within a six month time period

Secondary objectives:

* To determine the proportion of time SHS and mobile phones products are enabled among NVGs users * To assess the effect of NVGs on quality of life among Solar Home System users. * To measure the effect of NVGs on livelihood and income among Solar Home System users. * To determine the value that Solar Home System users attached to the solar lighting and daily/weekly time using it.

POPULATION Sun King SHS or mobile phone (purchased on credit) users, aged 40 years or above, with presbyopia, who purchased their product at least 3 months ago and have at least 6 months of repayments remaining.

INTERVENTION Provision of NVGs for presbyopia correction.

CONTROL Delayed provision of NVGs, presbyopia correction.

TIME FRAME 6 months

HYPOTHESIS Correcting presbyopia with NVGs improves the rate of SHS or mobile phone repayments made on time.

NULL HYPOTHESIS Correcting presbyopia with NVGs does not change the rate of repayments made or the proportion of time the participants have their system enabled.

STUDY DESIGN Randomised Control Trial.

STUDY AREA The study area includes rural, peri-urban and urban communities in Busia, Siaya, Vihiga and Kakamega in Western Kenya

SAMPLE SIZE DETERMINATION Mean solar product repayments to Sun King for the entry level category, products priced between KES 7,000 and 30,000, are KES 405 per month. To be able to identify a 10% difference in repayments between the groups, with a two-sided significance level of p=0.05 and power of 90%, a sample size of 461 per group is required. The investigators will screen 1,480 people, of which it is expected 1085 to meet the enrolment criteria. 543 will be randomly allocated to join the experimental group who will be provided their glasses at the start of the study and 543 will be randomly allocated to join the control group who will receive their glasses at the end of the study. The investigators expect the attrition rate to be similar across both groups, at \~15%. This will give us a final sample per group of at least 461.

SAMPLING PROCEDURES A software application will be used to randomly select whether participants go into the study or control group. The application will randomly select from the participants list, then randomly invite participants on one of two days per locality for the screening, provision of NVGs and baseline surveys. The day attended will determine participants' allocation to the glasses or control groups.

All participants on day two will receive glasses and all on day one do not (control). Neither group will be informed beforehand if they are receiving glasses or not; they will only be invited for a screening.

* Glasses will not be dispensed on the first day at each location and then will be dispensed on the second day. * When contacted, all participants will be invited for screening and told that they will receive eyeglasses at a date to be confirmed.

RECRUITMENT OF STUDY SUBJECTS

Sun King will call existing customers with the following criteria to invite them to participate in the study:

1. Aged over 40 years. 2. Purchased their product \>=3 months ago and have \>=6 months of repayments remaining on their PAYG contract. 3. The product is in the entry level category, priced between KES 7,000 and 30,000 (USD 46 and 196 at current exchange rates). 4. Reside in the counties of focus.

If they are willing to participate they will be asked if they have a pair of NVGs. If they do not have a pair, they will then be added to the initial participant list. If they have a pair, they will be excluded from selection. The selected study participants will be asked to complete and sign a consent form prior to the initial assessment and then randomly allocated to the experimental or control group.

Participants will receive compensation for travel expenses of 300 KSH

Data collection methodology

The data collection will be primarily quantitative. The data will be collected through:

1. Sun King's customer relationship management system, which records each client's product details, repayment schedule, payment details and the duration of the product's activation. This will be shared for analysis in a spreadsheet. 2. Individual surveys, using a semi-structured questionnaire. The surveys will be conducted in-person using Kobo Toolbox on mobile devices. 3. NVA test.

RESEARCH STAFF TRAINING

1. For the study the study team will be working with GMaurich Insights, a social research agency whose data scientists have over 20 years of combined experience. 2. GMaurich will provide Research Assistants (RAs) for the study. 3. DOT Glasses take the RAs through a 1-day training. The curriculum will cover:

1. Research ethics and informed consent. 2. Introduction to eye health and visual acuity. 3. How to screen using the NVA chart. 4. How to assess, at a basic level, if there may be more complicated eye conditions, and the referral process for other eye issues. It will be made clear to participants that this vision screening does not constitute a thorough ophthalmic examination, and that they should seek assessment for other visual/ocular symptoms elsewhere. 5. How to distribute the glasses. 6. Explaining to participants how to use the glasses and which tasks they should/should not be used for. 7. Going through the question set. 4. GMaurich RAs will then need to pass a DOT Glasses practical assessment to be able to distribute the glasses.

DATA COLLECTION

1\. A sample of 20 surveys will be completed to pilot the tool and stress-test the process.

2\. Participants will be invited to a convenient location for the data collection. Depending on the day, the participants will be assigned to either the study or control group.

3\. Data collection procedure in the field:

1. The RAs will explain the study purpose and process to the participant, and obtain written, informed consent before proceeding. 2. Conduct a DVA test with participants needing to achieve a minimum of 20/40. 3. Conduct a NVA test using Precision Vision Near Vision Chart:

i. Test presenting Near Visual Acuity. ii. Assess required near correction lens power (dioptres). iii. Retest corrected NVA. iv. Refer to a specialist if:

1. The participant has NVA worse than N6 at 40 centimetres and is not correctable by any of the available lenses. 2. The participant has other visible ocular pathology. d. Conduct the survey. e. For the study group: i. Provide the correct power and fit the glasses. ii. If no NVGs are required, offer sunglasses for their time and participation. f. For the control group: i. Assess the correct power, but delay glasses provision. ii. The eyeglasses will be provided at the end line.

4\. Follow up period:

a. Intervention group: i. At 3 months participants will have an over the phone follow up to ask whether or not they are using the glasses.

ii. At 6 months follow up questionnaire and eye screening in person. b. Control group: i. At 6 months followed up questionnaire, eye screening and distribution of glasses.

• Vision related quality of life [Time frame: Measured at baseline and end of the study (6 months)]
• Income [Time frame: Measured at baseline and end of the study (6 months)]
• Livelihood [Time frame: Measured at baseline and end of the study (6 months)]