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農村部の高校進学率を高めるために中学生の近視を矯正する (SWISH)

2026年11月3日 更新者:Nathan Congdon、Queen's University, Belfast

SWISH (See Well to Stay In ScHool): 農村部の高校への進学率を高めるため、近視のある中学生に眼鏡を配布するランダム化試験)

Chinese children are some of the most short-sighted in the world, but only one in five children in poor areas who needs glasses has them. Our team has already shown in other trials that giving children free glasses leads to better grades and that free glasses have a bigger impact on grades than factors like parents' education level and the amount of money a family has. The effect on grades from glasses is greater than from other health services in school, like giving vitamins. Only about one in three children in rural China goes on to a regular, non-vocational high school. The investigators would like to show the Chinese government strong evidence of what glasses can do to help children continue their education, in order to help convince the government to carry out national programs to provide free glasses for children who need them.

Study Plan: The investigators will choose 111 middle schools at random in Liaoning, northern China, and all children in Year 1 at each school will go at random into one of two groups: either a group getting free glasses, with support from teachers to push them to wear the glasses ("Intervention") or a group getting just glasses prescriptions ("Control.") The main study outcome will be the proportion of children going on to academic (as opposed to vocational) high school, and the study is powered to detect a 10% difference in this figure between groups.The study will also assess whether children wear their glasses at school and how often they use blackboards (which disadvantage short-sighted children) vs textbooks to learn from. These other outcomes will help us to better understand the causal pathway between vision and high school attendance. We will also study the total cost of providing glasses and the teacher support to wear them per additional student attending academic high school, as well as student mental health outcomes. We will also collect data on the progression of nearsightedness. The hypothesis of this study is that providing glasses will increase academic high school attendance.

調査の概要

状態

積極的、募集していない

条件

詳細な説明

Research question: Will providing free glasses to myopic rural Chinese students, with a teacher incentive to promote use, increase academic high school attendance?

Design: Cluster-randomised controlled trial

Rationale: Rural Chinese children have high myopia prevalence, but poor access to glasses. Our previous trials show giving free glasses significantly improves academic performance, with greater effect size than parental education or family income, equaling or exceeding other classroom-based medical interventions. Non-vocational (academic) high school attendance is only 30% in rural western China. Strong evidence of educational benefit from glasses is needed to spur adoption of national distribution programs.

Methods: Children in Year 1 at 111 randomly-selected middle schools in Liaoning, Northern China, will be randomized by school to receive free glasses and a trial-proven teacher-based incentive to promote wear (Intervention) or prescriptions only (Control). The main outcome 3 years later will be high school attendance (powered to detect 10% difference between study groups); secondary outcomes of compliance and use of near versus distance classroom learning aids will elucidate biological plausibility of a causal pathway between myopia correction and learning. Local knowledge and attitudes about myopia and spectacle use and intervention cost-effectiveness will be studied.

Statistical methods to be employed in the analysis and justification for the choice of sample size:

Adjusted- and unadjusted-comparison of the difference between study groups

Principal analyses for the main trial will include:

  • Of attendance at academic high school after Year 3 of middle school (as opposed to following a vocational pathway or leaving school).
  • of observed spectacle wear at un-announced examinations at school and for self-efficacy scores.
  • of mental health outcomes after Year 1 year of intervention

Sample size: Assuming 120 students per school undergoing vision screening, 50% of children failing vision screening, 30% of these needing glasses, α=0.05, intra-class correlation=0.10, explained variation by covariates=0.40, difference between the groups in the main study outcome=10%, high-school attendance rate in the Control group=50%, a sample size of 111 middle-schools (55 or 56 in each group) will provide power=80%.

Loss to follow-up in our previous school-based trials in China, SWLW I and II, was approximately 4% over the course of one school year, and so our calculations here assume a loss to follow-up of 10% over 2-3 years. However, we have not adjusted for non-compliance because we will use a strict intention-to-treat analytic approach where children in schools allocated to the Intervention group will be analysed as such irrespective of compliance and because our intention is to test the policy of making free glasses available to those students who need them, rather than the effect of those students actually wearing the glasses. Further, our expected effect size is based conservatively on previous trials with compliance rates of approximately 40%, which we feel can be improved on in the current trial with teacher incentives as above.

研究の種類

介入

入学 (推定)

10000

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Northern Ireland
      • Belfast、Northern Ireland、イギリス、BT12 6BJ
        • Centre for Public Health
    • Liaoning
      • Shenyang、Liaoning、中国、110163
        • He Eye Specialist Hospital
    • Xixia
      • Yinchuan、Xixia、中国、750021
        • Ningxia University

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳未満 (子、大人)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Year 1 classes (likely age 12-15 years) at the recruited schools
  • Those who will be in the second year of middle school when the intervention begins the next year
  • Have uncorrected (without glasses/presenting) visual acuity of ≤6/12 in both eyes
  • Refractive error meets cut-offs shown to be associated with significantly greater improvement in visual acuity when corrected (myopia ≤-0.75 diopters (D, or astigmatism (non-spherical refractive error) ≥1.00 D)
  • Visual acuity can be improved to >= 6/7.5 in at least one eye with glasses.

Exclusion Criteria:

  • Hyperopia ≥ 2.00 D
  • Presence of visually-significant ocular condition besides refractive error

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:ダブル

武器と介入

参加者グループ / アーム
介入・治療
実験的:Intervention

Children at Intervention schools will receive free spectacles of a design they select, based on the child's measured refractive power and dispensed at school by the study optometrist. Additionally, teachers (but not children) in eligible classes will be informed that if 80% spectacle compliance as measured across three separate unannounced inspections was achieved, they will be given an incentive of an conditional cash transfer. The cash transfer will be deposited into the teacher's bank accounts directly.

Intervention group children in middle school Year 1 will receive spectacles in December 2024. Assuming that the relevant effects of treatment (glasses wear) on the main study outcome are complete once examinations determining high school attendance are finished at the end of Middle School Year 3, Intervention participants will have undergone 32 months (December 2024 - July 2027) of treatment by the endpoint of the trial.

他の名前:
  • 眼鏡
介入なし:Control

Children at Control schools will receive a glasses prescription and letter to the parents informing them of the refractive status of their child, with free glasses provided only at the end of the trial. No teacher incentive will be offered. Service offered to the Control group exceeds standard care, in that no school-based programs of vision screening and refraction currently exist in the study area, or in most of rural China.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Academic high school attendance
時間枠:In July following completion of Year 3 of Middle School. This occurs after 32 months of participant followup.

Proportion of children who continue to academic high school as opposed to vocational high school or no additional schooling, assessed by systematically contacting parents, teachers and students to ascertain enrolment status

In July following completion of Year 3 of Middle School. This occurs after 32 months of participant followup.

二次結果の測定

結果測定
メジャーの説明
時間枠
Compliance with spectacle wear
時間枠:After 12 months of participant followup

Actual presence of spectacles on the child's face (rather than having glasses at school) at the time of an unannounced examination.

After 12 months of participant followup
Blackboard use
時間枠:After 12 months of participant followup

Frequency of blackboard versus textbook use on a questionnaire administered to class teachers, and answered as "all", "most", "about half", little" or "none" of teaching.

After 12 months of participant followup
Cost effectiveness of intervention.
時間枠:At study closeout, after 32 months of participant followup

Calculated as ratio of incremental cost to proportion of children who continue to academic high school as opposed to vocational high school or no schooling. Incremental cost is the difference of costs between implementation of intervention and control. Intervention costs will comprise the screening test, glasses (including replacements) and teacher incentives.

At study closeout, after 32 months of participant followup
Depression and Anxiety
時間枠:At baseline and 12 months post-treatment

Depression and anxiety score measured with Anxiety Stress Scale (DASS). The score range for depression, anxiety and stress are 0-42, with higher score indicates more severe mental health problems.

At baseline and 12 months post-treatment
Self Esteem
時間枠:At baseline and 12 months post-treatment

Self-esteem score measured with the Rosenberg Self-esteem Scale. The scores range from 0-30, with higher scores indicate higher self-esteem.

At baseline and 12 months post-treatment
Emotional and behavioral problems
時間枠:At baseline and 12 months post-treatment

Emotional and behavioral problems score using the Strengths and Difficulties Questionnaire (SDQ), with difficulties score ranges from 0 to 40, Prosocial scale ranges from 0-10, with higher score indicates severe mental health and behavioral problems.

At baseline and 12 months post-treatment
Progression of Shortsightedness
時間枠:At baseline and 12 months post-treatment

Progression of Shortsightedness will be measured using change in refraction over time

At baseline and 12 months post-treatment
Parents' and students' attitude towards spectacle wear
時間枠:After baseline

The primary data collection instruments are two tailored, semi-structured interview guides: one designed for the parents/guardians, and one developmentally adapted for the students. Rather than utilizing rigid survey questions, these qualitative instruments are comprised of open-ended prompts, scenarios.

The students interview guide has been specifically adapted for 7th-grade students (aged 12-13). It utilizes age-appropriate terminology and focuses heavily on adolescent-specific barriers, such as peer pressure, cosmetic concerns, and school dynamics.

After baseline

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2024年11月28日

一次修了 (推定)

2027年8月30日

研究の完了 (推定)

2027年8月30日

試験登録日

最初に提出

2019年8月7日

QC基準を満たした最初の提出物

2019年8月29日

最初の投稿 (実際)

2019年9月4日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月4日

QC基準を満たした最後の更新が送信されました

2026年11月3日

最終確認日

2026年11月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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