Online Video Training for Teachers to Improve Reading Skills in Children Using Augmentative and Alternative Communication

February 16, 2025 updated by: Ostfold University College

The aim of this study is to investigate , via a randomized control trial (RCT), the effectiveness of an online video training platform designed for teachers to support the improvement of basic reading skills of children with intellectual disabilities (ID) who require augmentative and alternative communication (AAC). This intervention will include 14 schools and 70 students with ID who require AAC age 6-14 years old. The research question is:

1) What is the difference between online video training and in-person training on improving word-level readig skills and phonological awareness?

The students will work with a reading material, Reading for All, that follow the strategies of Accessible Literacy Learning, developed by Janice Light and David McNaughton. Reading for All is based on the research of Janice Light and David McNaughton. The reading material are adapted for AAC-users and the students can answer with pointing or their AAC-systems. Teachers will implement the instructions at the students familiar place at school for three to five days, each week, for a year.

The reading material consist of tasks in sound blending, letter-sound correspondence, phoneme segmentation, sight words, shared reading and decoding. The teachers will use evidence based, systematic and explicit instructions and immediate and corrective feedback

Study Overview

Status

Enrolling by invitation

Detailed Description

Children with disabilities who require AAC may experiance challenges in various areas development, including communication skills, speech, language, cognitive and conceptual development, literacy, social participation, access to education, and overall quality of lifte. Acquiring reading skills may lead to higher levels of communication. Students who require AAC may be more dependent on others to provide and teach symbols to represent their language. Acquireing reading skills, may incrace the possibility to independently express themselves, and increace their access to for example text based communication devices.

There is a laci of evidence-based reading material adapted for students with ID who require AAC.

Primary outcomes will be assessed six times every two months over one year. The reading test are based on the reading material, which will be validated before the beginning of the trial.

Secondary outcome: four-time points (baseline, fourth, eighth, and twelfth month).

Study Type

Interventional

Enrollment (Estimated)

70

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Halden, Norway, 1757
        • Østfold University College

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • ages 6-14 years,
  • diagnosed with intellectual disability, confirmed by multidisciplinary assessments carried out by the Child rehabilitation service,
  • not have a functional speech, i.e. require AAC to understand and make oneself understood,
  • must use AAC as their primary form of communication,
  • cannot follow ordinary curricula (LK20) but have their own education plan.

Exclusion Criteria:

  • having a severe visual impairment and not being able to decode single words (e.g., severe hearing impairment).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Video training for teachers
It is 14 schools and they will be randomized into two groups. The teachers at seven schools will receive video training on how to carry out the reading intervention.

Reading intervention over a year for students with intellectual disabilities who use AAC. This study included teachers from 14 different schools and 8 municipalities and their students. It is two arms in the intervention, with approximately 7 schools and their teachers in "video training for teachers" and "in person mentoring for teachers". The schools are randomized into these two groups, but in both groups, they will carry out the same intervention.

The students in both groups will work explicitly and systematically with the reading material "Reading for all", which is based on the research of, among others, Janice Light and David McNaughton, and their reading program "Accessible Literacy Learning (ALL)".

Experimental: In-person mentoring for teachers
It is 14 schools and they will be randomized into two groups. The teachers at seven schools will receive in-person training on how to carry out the reading intervention

Reading intervention over a year for students with intellectual disabilities who use AAC. This study included teachers from 14 different schools and 8 municipalities and their students. It is two arms in the intervention, with approximately 7 schools and their teachers in "video training for teachers" and "in person mentoring for teachers". The schools are randomized into these two groups, but in both groups, they will carry out the same intervention.

The students in both groups will work explicitly and systematically with the reading material "Reading for all", which is based on the research of, among others, Janice Light and David McNaughton, and their reading program "Accessible Literacy Learning (ALL)".

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Early reading skills outcome
Time Frame: From intervention start to the end of intervention at twelve months

Primary outcome will be assessed six times every two months over one year.

  • Sound blending [score ranging from 0 to 15] involves testing the student's ability to combine individual sounds into words.
  • Letter-sound correspondence [score ranging from 0 to 25] involves testing the students' ability to correspond between the sounds of speech (phonemes) and the written letters representing speech (graphemes).
  • Phoneme segmentation [score ranging from 0 to 20] tests students' ability to segment the first phoneme of the word (e.g., s for sun).
From intervention start to the end of intervention at twelve months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Reading outcome
Time Frame: From intervention start to the end of intervention at twelve months

The Secondary Outcome: four-time points (baseline, fourth, eighth, and twelfth month).

  • Recognition of sight words [score ranging from 0 to 20] measures the student's ability to recognize words learned by sight.
  • Decoding [score ranging from 0 to 20] evaluates students' ability to recognize the letters in the word, associate each letter with its corresponding sound, hold these sounds in sequence in working memory, blend the sounds to determine the word, retrieve the meaning of the word.
From intervention start to the end of intervention at twelve months
Vocabulary
Time Frame: From intervention start to the end of intervention at twelve months
The teachers will map the students communicative competance by using MacArthur-Bates Communicative Development Inventories (MCDI before and after the reading intervention to measure development of vocabulary. Score range for word and gestures have 391 words and word and sentences have 731 words.
From intervention start to the end of intervention at twelve months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Hugo Cogo Moreira, Professor, Ostfold University College

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 25, 2024

Primary Completion (Estimated)

March 17, 2025

Study Completion (Estimated)

March 18, 2026

Study Registration Dates

First Submitted

November 29, 2024

First Submitted That Met QC Criteria

January 3, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 16, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Following the FAIR Data Principles, the trial protocol, its registration, and models created to analyze the data during the project will be made available on platforms such as OSF and https://clinicaltrials.gov/. Project objectives and results will be communicated to the general public through newsletters, social media, mainstream media (regional newspaper), and presentations at showcase events. Lastly, we plan to launch a publicly accessible website of the project, describing the project, including its goals and the partners.

IPD Sharing Time Frame

Study protocol: January 2025- August 2027 Statistical analysis Plan: May 2026- August 2027 Analytic Code: June 2026- August 2027

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ANALYTIC_CODE

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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