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临床试验/NCT02861599
NCT02861599Unknown不适用

Study of the Interest of Proprioceptive Therapy as a Complement to Speech Therapy in Children With Reading Difficulties

Centre Hospitalier Universitaire Dijon2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2015年9月最近更新:
适应症

试验速览

阶段
不适用
入组人数
150
试验地点
2
主要终点
Percentage of children who had stabilized their delay in reading acquisition at the Timé-3 test (identification of written words)

研究概览

简要总结

Before proposing this observational study protocol, a randomized study was attempted. This consisted in proposing to families of children with difficulties in learning to read, via the speech therapists who were treating them, to take part in a randomized trial that compared speech therapy alone with a combination of speech therapy and proprioceptive therapy. If parents agreed in principle with the study, the child underwent a complementary speech therapy examination and was referred to the nearest investigating doctor for inclusion. However, this study had to be abandoned because of insufficient recruitment (2 patients included in 1 year). Despite the motivation and training of participating speech therapists, proposing a study based on randomization to families often in distress proved to be extremely difficult, as their conviction of the interest of proprioceptive therapy was greater than the available scientific evidence suggested. Direct recruitment by investigating ophthalmologists was not possible because they were consulted directly by the families so as to obtain proprioceptive therapy. The principle of randomization would thus not have been accepted.

In light of the above, we decided to turn towards a non-randomized study comparing outcomes in two groups of children:

  • children who consulted an ophthalmologist who proposed proprioceptive therapy in Côte d'Or
  • children managed by one of the four speech therapists who do not propose proprioceptive therapy and who accepted the principle of the study.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
盲法
None

入排标准

年龄范围
7 Years 至 11 Years(Child)
性别
All
接受健康志愿者

入选标准

  • For both groups:
  • children at school and between the end of year 3 and the end of year 7
  • with speech therapy for reading difficulties
  • with a delay of 18 months or more compared with children in the same group at inclusion
  • who had never had proprioceptive therapy
  • in cases of two or more siblings with reading difficulties between year 3 and year 8, only one child will be included.
  • With one speech therapy session per week
  • Who have accepted to take part in the study in agreement with their parents
  • With national health insurance cover For the " speech therapy only" cohort: children followed by speech therapists who do not usually refer their patients to ophthalmologists that use proprioceptive therapy in cases of delayed reading acquisition and have not previously consulted an ophthalmologist proposing this type of therapy.
  • For the " speech therapy associated with proprioceptive therapy " cohort: children with reading difficulties followed by a speech therapist and consulting for the first time an ophthalmologist, study investigator, who uses proprioceptive therapy in the treatment of reading difficulties.

排除标准

  • Children who lack motivation and/or and those unlikely to be followed in optimal conditions
  • Neonatal distress: APGAR <7
  • Gestational age < 37 weeks of Amenorrhea (WA)
  • Genetic disease
  • Known abnormal or delay in psychomotor development
  • Psychiatric disorder
  • Sensory deficit or disorder known to limit the possibilities of proprioceptive therapy
  • Children undergoing treatment, notably psychotropic agents, Ritaline®, antiepileptic agents or rehabilitation, which may interfere with reading difficulties or the therapy proposed in the study
  • Children in special needs schools (SEGPA)
  • Children who cannot attend all of the consultations planned in the protocol for practical reasons.

结局指标

主要结局

Percentage of children who had stabilized their delay in reading acquisition at the Timé-3 test (identification of written words)

时间窗: At month12

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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