REEDVAC: Effectiveness of a Parent-administered Reading Therapy Program During Summer Break for Dyslexic Children

Sponsor
Assistance Publique - Hôpitaux de Paris (Other)
Overall Status
Completed
CT.gov ID
NCT04384952
Collaborator
(none)
22
1
2
4.3
5.1

Study Details

Study Description

Brief Summary

"After summer break, the reading performance of dyslexic children declines more than those of non-dyslexic children. Indeed, during the summer, dyslexic children are less inclined to read and their consultations with speech therapist are usually suspended.

Intensive speech therapy programs proved to be efficient during the summer, to maintain reading level of dyslexic children. However these programs are expensive and not easy to generalise. Some other studies tested reading therapy programs applied by parents at home. It proved to be effective and feasible.

Thus, the hypothesis of the present study is: a parent-administered reading therapy program during the summer break could stabilise the reading performance of dyslexic children after the summer. On the contrary the investigators assume the control group reading performance would decrease."

Condition or Disease Intervention/Treatment Phase
  • Other: Parent-administered reading therapy.
  • Other: Dyslexic's Holiday Workbook
N/A

Detailed Description

"Dyslexia is a specific learning disability characterised by reading difficulties, not caused by developmental, neurological or sensory (vision or hearing) disorders.

After summer break, the reading performance of dyslexic children declines more than those of non-dyslexic children. Indeed, during the summer, dyslexic children are less inclined to read and their consultations with speech therapist are usually suspended.

Intensive reading therapy programs proved to be efficient during the summer, to maintain reading level of dyslexic children. However these programs are expensive and not easy to generalise. Some other studies tested reading therapy programs applied by parents at home. It proved to be effective and feasible.

Thus, the hypothesis of the present study is: a parent-administered reading therapy program during the summer break could stabilise the reading performance of dyslexic children (grade 3 to 5) after the summer. On the contrary the investigators assume the control group reading performance would decrease.

With a controlled randomised trial, the investigators will compare the reading performance of two groups of dyslexic children with the same type of dyslexia (with visual information treatment deficit). All of them are diagnosed by the Reference Centre for learning disabilities (CRTLA), a Robert Debré Hospital's Unit, Paris (France).

Intensity and duration : 6 weeks during the summer break. 15 minutes/day, 5 times per week.

Intervention group : Parent-administered reading therapy program. Control group : Dyslexic's Holiday Workbook (Hatier Editor). This study's main objective consists in evaluating the effectiveness in reading performance of a parent-administered reading training program during the summer break for dyslexic children.

"

Study Design

Study Type:
Interventional
Actual Enrollment :
22 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
Single Blind
Primary Purpose:
Treatment
Official Title:
Randomized Controlled Trial Comparing the Effect of a Parent-guided Speech and Language Therapy Program During the Summer Holidays With an Adapted Holiday Book on the Reading Level of Children With Visual-attentional Dyslexia
Actual Study Start Date :
Jun 5, 2020
Actual Primary Completion Date :
Oct 15, 2020
Actual Study Completion Date :
Oct 15, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Parent-administered reading therapy.

Parent-administered reading therapy program: 15min each day, 5 days a week during 6 weeks during the summer break. Repeated reading with feedback from the parent and time control.

Other: Parent-administered reading therapy.
Parent-administered reading therapy program: 15min each day, 5 days a week during 6 weeks during the summer break. Repeted reading with feedback from the parent and time control.

Active Comparator: Dyslexic's Holliday Workbook.

Use of a special Dys holiday book, no parent-guided training.

Other: Dyslexic's Holiday Workbook
Use of a special Dyslexic's holiday book, no parent-guided training.

Outcome Measures

Primary Outcome Measures

  1. Measuring program effectiveness on reading performance (accuracy and speed of word reading) [4 weeks]

    Word Reading performance with French BALE Test. BALE (Batterie Analytique du Langage Ecrit). Measure of number of correct words read and speed of reading. Raw score for word reading performance (accuracy) : minimum 0 (worse outcomme, maximum 20 (better outcome)

Eligibility Criteria

Criteria

Ages Eligible for Study:
8 Years to 13 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Schooled in Grade 3, 4 or 5 (CE2, CM1 ou CM2) at inclusion

  • Diagnosis of developmental dyslexia with visual information treatment deficit, confirmed by the Reference Center for Learning Disabilities, Robert Debré Hospital

  • Speech therapy for dyslexia that has started for at least 6 months

  • No speech therapy during the 6-weeks intervention

  • Family interest and availibility for 6 weeks durant summer break

  • Informed consent signed by parents

  • Affiliation to a social security scheme

Exclusion Criteria:
  • Parents not fluent enough in French to read a text

  • Patient IQ (intelligence quotient) < 70 (WISC test- Wechsler Intelligence Scale for Children)

  • Other neurological pathology in the foreground

  • Presenting hearing disorders or visual disorders not treated,

  • Member of a sibling also eligible for the protocol (contamination bias)

  • Beneficiary of State medical aid (AME)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Robert Debre Hospital Paris France 75019

Sponsors and Collaborators

  • Assistance Publique - Hôpitaux de Paris

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT04384952
Other Study ID Numbers:
  • APHP200214
  • IDRCB 2019-A03260-57
First Posted:
May 12, 2020
Last Update Posted:
Oct 18, 2021
Last Verified:
Apr 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 18, 2021