The Influence of Immersive Virtual Field Trips on Academic Vocabulary

April 11, 2023 updated by: Salus University

The Influence of Immersive Virtual Field Trips on Academic Vocabulary for Early Elementary Students With Developmental Language Disorder

The purpose of this study is to investigate an immersive virtual field trip (iVFT) on topic specific academic vocabulary for students with developmental language disorder (DLD). DLD is the most common childhood learning disorder with a prevalence of 7.4%(1) and occurs in the absence of a known biomedical condition (e.g., hearing loss, autism, stroke, intellectual disability). DLD affects a person's academic and social function due to difficulty with using and understanding language.(2,3) Approximately half of students with DLD have a deficit in vocabulary that persists through highschool.(4) Once children fall behind in their language and vocabulary development, it is very difficult to catch up generally resulting in a wider gap as they progress through their school years. This deficit can have cascading social, mental health, occupational and financial consequences.(5) There is preliminary evidence that a virtual reality experience such as an immersive virtual field trip (iVFT) was beneficial for facilitating vocabulary and comprehension in general education(6-8) and within targeted populations of students including second language learners(9) and those with learning differences (e.g., autism,(10) attention deficit hyperactivity,(11,12) and dyslexia(13). The term "immersive" refers to a state of heightened sensation when viewing a simulated environment that is superimposed onto a screen with embedded multisensory input (e.g., visual, auditory, proprioceptive).(14) The viewer looks through 3D goggles to block out the present environment resulting in a feeling of presence. These simulated experiences or destinations (e.g., space) are a type of VR referred to as an immersive virtual field trip (iVFT).

To date, there is a lack of empirical evidence, explicitly targeting academic vocabulary growth for early grade school students with DLD. In addition, no study has reported on learning outcomes of students with DLD following a VR condition. Therefore, the primary study objective was to compare gains in academic vocabulary measures between a traditional book condition and an iVFT learning condition for young students with DLD.

Study Overview

Detailed Description

The purpose of this randomized control study is to investigate an immersive virtual field trip (iVFT) for learning academic vocabulary for students with developmental language disorder (DLD).

The primary objective is to compare gains in topic specific vocabulary measures between a traditional book condition and an iVFT learning condition. Also, this study will compare perceptions of the study experience between the control and experimental groups.

At study entry, 24 children between the ages of 6:0 to 8:12 years old with a developmental language disorder (DLD) will be randomized to equal groups of control book and experimental iVFT conditions.

If satisfy the inclusion and exclusion criteria, a three-phase pre-enrollment process will ensue. In the first phase, the Student Language Scale (SLS) and Shaywitz Dyslexia screeners will be administered to determine likelihood of presence of a language disorder and functional impact on academic and social growth. In the second phase, the CELF-5 diagnostic language assessment will determine the presence of a DLD if a standard score equal or less than 75 is obtained. In the third phase, the PPVT-5 vocabulary assessment will be administered to provide additional information about general receptive vocabulary knowledge. Lastly, four topic specific vocabulary measures will provide a measure of baseline topic vocabulary knowledge.

Consented and enrolled participants will be randomized into equal groups of control and experimental conditions. The control group will receive a pre-read book and the experimental group will be exposed to an immersive virtual field trip using 3D cardboard goggles and a smart phone. The content in the book and iVFT parallel one another. In both groups, audio and visual stimuli are presented. For all participants, a total of three 15-minute exposures will occur.

Following the condition, the four-topic specific vocabulary measures will be repeated to report on vocabulary growth. The measures include:

  1. Divergent Naming (expressive): "Tell me the names of as many [topic] as you can think of, as quickly as possible, in one minute."
  2. Word Naming (expressive confrontational naming): State name of target image presented in isolation.
  3. Picture Identification (receptive): Identify target picture in field of ten.
  4. Word meaning recognition: Match the word with the written meaning. Lastly, all participants will rate experience their experience using an Intrinsic Motivation Inventory (IMI) with a 5-point Smile Likert Scale.

The data analysis will include descriptive and inferential statistics to report within and between group gains in the four-topic specific vocabulary measures.

Study Type

Interventional

Enrollment (Actual)

30

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

    • Pennsylvania
      • Elkins Park, Pennsylvania, United States, 19027
        • Salus University

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

6 years to 8 years (Child)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Age 6.0- 8.12 years.
  • English language proficiency determined by examiner screening.
  • Spoken language is readily understandable by examiner.
  • Child speaks at least five-word sentences per examiner screening.
  • Child understands and can follow two-part directions per examiner screening.
  • Subject can complete all study protocol assessments.
  • Sees single image in binoculars and sees 3D images.
  • Diagnosis of developmental language disorder (DLD) (determined by ≤-1SD on the Clinical Evaluation of Language Fundamentals (CELF-5) completed within the past 12 months or examiner evaluation with the CELF-5.
  • Vocabulary deficit determined by scores equal to or less than 30% on two or more topic specific vocabulary measures.
  • Access to home Wi-Fi with sufficient connectivity to run the iVFT
  • VFT compatible smartphone to include operating systems iOS 8.0 (e.g., Apple iPhone 6 or later) or later or Android 4.1 (JellyBean) or later (e.g., Samsung Galaxy S5 or later).

(Note: If a participant would otherwise not be able to participate, a loaner device will be provided to the parent/guardian for study purposes.)

Exclusion Criteria:

  • History of the following medical conditions

    • Seizures/epilepsy
    • Moderate to severe motion sickness, cybersickness
    • Vision impairment defined as any child who has 504 plan requiring accommodations for visual impairment
    • Hearing impairment that prevents a child from hearing audio on a mobile device, a history of a failed hearing screening that has not been resolved, or a hearing impairment that results in an educational impact and requires specially designed instruction under IDEA (34 CFR § 300.8)."
  • Inability to use the smart phone application
  • Classified by school district as LEP (limited English proficient).
  • Children who are wards of the state or any other agency, institution, or entity will not be solicited for participation.
  • Intellectual disability (based on IEP/504 status).

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Book condition
Participants in the control condition will be receive a pre-recorded audio-visual book presentation. The purpose of pre-reading is to provide consistency in the examiner's affect and presentation, thereby controlling for potential examiner effects on study outcomes. Participants in the control group will receive three interventions each lasting 15-minutes. The number of sessions and intervention time is equal for both the control and experimental groups. The information provided in the control book and experimental iVFT parallel one another.
Experimental: Immersive virtual field trip (iVFT)
The study intervention is a multisensory immersive virtual reality trip to the moon. Participants will use 3D cardboard goggles and a smart phone. No additional interventions will occur. Participants in the iVFT experimental group will receive three interventions each lasting 15-minutes. The number of sessions and intervention time is equal for both the control and experimental groups. Participants will explore the moon through a virtual reality scene by moving their body and head, which creates a 360º view. When hovering over items, participants are presented with several key elements related to word learning (e.g., written and spoken words/narrative). Multiple items are given extra emphasis through hotspots that provide audiovisual content in the form of brief videos and spoken scripts. The information provided in the iVFT and control book parallel one another.

An immersive virtual fled trip (iVFT) is a form of virtual reality (VR). The term immersive refers to an experience where the senses become heightened through multisensory input (e.g., visual, auditory, proprioceptive). When adding peripherals such as a head-mounted device (HMD) (e.g., goggles with 3D-lenses), a mobile phone becomes a pseudo-theater providing a 360-degree view that mimics the real world. For example, one can experience a simulated rollercoaster or visit the moon that may otherwise be inaccessible in day-to-day life. Also, a VFT provides for context and aids in background knowledge that is a crucial aspect of learning.

Participants will receive three interventions sessions each last 15-minutes.

Other Names:
  • Virtual Reality (VR)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Compare vocabulary gains between the book and iVFT conditions
Time Frame: 1 week: pretest, three 15-minute intervention sessions, posttest

Change in target vocabulary words from pre to post intervention between the control book condition and the iVFT learning condition. Four-topic specific omnibus vocabulary measures include:

  1. Divergent Naming (expressive): "Tell me the names of as many [topic] as you can think of, as quickly as possible, in one minute." One point earned for each named word.
  2. Word Naming (expressive confrontational naming): State name of target image presented in isolation. One point earned for each correct response.
  3. Picture Identification (receptive): Identify target picture in field of ten. One point earned for each correct response.
  4. Word meaning recognition: Match the word with the written meaning. One point earned for each correct response.
1 week: pretest, three 15-minute intervention sessions, posttest

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Vocabulary growth following an iVFT condition
Time Frame: 1 week: pretest target vocabulary, three 15-minute intervention sessions, posttest target vocabulary

To determine if an iVFT is effective for improving topic-specific vocabulary four omnibus vocabulary measures will be conducted pre-treatment and re-administered post-treatment.

omnibus vocabulary measures include:

  1. Divergent Naming (expressive): "Tell me the names of as many [topic] as you can think of, as quickly as possible, in one minute." One point earned for each named word.
  2. Word Naming (expressive confrontational naming): State name of target image presented in isolation. One point earned for each correct response.
  3. Picture Identification (receptive): Identify target picture in field of ten. One point earned for each correct response.
  4. Word meaning recognition: Match the word with the written meaning. One point earned for each correct response.
1 week: pretest target vocabulary, three 15-minute intervention sessions, posttest target vocabulary
Compare group perceptions of the study experience.
Time Frame: 1 week: following three 15-minute intervention sessions
Following post vocabulary testing, participants will rate their experience by responding to a 15 question Intrinsic Motivation Inventory (IMI) with a 5-point Smile Likert Scale.
1 week: following three 15-minute intervention sessions

Collaborators and Investigators

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

Investigators

  • Study Chair: Mitchell Scheiman, PhD, DO, Dean of Research
  • Study Chair: Amy Lustig, PhD,SLP,MPH, Salus Univeristy
  • Principal Investigator: Yvonne D'Uva Howard, PhD, MS SLP, Salus University

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)

October 7, 2021

Primary Completion (Actual)

March 1, 2022

Study Completion (Actual)

June 6, 2022

Study Registration Dates

First Submitted

January 23, 2022

First Submitted That Met QC Criteria

February 6, 2022

First Posted (Actual)

February 16, 2022

Study Record Updates

Last Update Posted (Actual)

April 12, 2023

Last Update Submitted That Met QC Criteria

April 11, 2023

Last Verified

February 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

IPD will not be shared

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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