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DeafnessNCT05993832

Word Learning in Deaf Children Using Eye-tracking and Behavioral Measures

A study testing input cue in people with Deafness, run by Boston University Charles River Campus at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Mutual exclusivity is a word learning constraint in which the learner assumes that a given word refers to only one category of objects. In spoken languages, mutual exclusivity has been demonstrated in monolingual children as young as 17 months and cross-linguistically, while multilingual learners show an attenuated… Read more about this study

Who is it for?
Ages 18 to 60 months
Conditions the study is for
Deafness
What is being tested?
input cue
Could I receive a placebo?
No, everyone receives an active treatment
How many people
48 participants
Where
1 siteUnited States
Study dates
7 Aug 2023to 20 Jun 2025
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 months
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Deaf children ages 18-60 months
  • born severely to profoundly deaf
  • have either deaf or hearing parents
  • communicate using American Sign Language
  • have normal to corrected normal vision

Who cannot join

  • Deaf children who have not been exposed to American Sign Language

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Boston University

    Boston, Massachusetts, 02215

Other trials in United States

About this study

Mutual exclusivity is a word learning constraint in which the learner assumes that a given word refers to only one category of objects. In spoken languages, mutual exclusivity has been demonstrated in monolingual children as young as 17 months and cross-linguistically, while multilingual learners show an attenuated mutual exclusivity bias. Mutual exclusivity has not been robustly demonstrated in deaf children acquiring American Sign Language (ASL). Further, it is unclear if mutual exclusivity applies to those learning both a signed and a spoken language. Like unimodal bilinguals, bimodal bilingual (BiBi) children learn two words for an object, but these words are separated by modality. A BiBi child could therefore assume that all objects have two words (like unimodal bilinguals) or that all objects have one spoken word and one sign (within-modality mutual exclusivity). The goals of the current study are to demonstrate mutual exclusivity in monolingual deaf children acquiring ASL, and to determine if BiBi deaf children utilize mutual exclusivity within each modality.

Read the detailed description

The investigators will investigate how deaf children prioritize input cues to word meaning when linguistic cues (i.e. mutual exclusivity) and referential gaze are in conflict in a structured word learning task.

Participants: Deaf children (n=40) ages 18 to 60 months are eligible to participate. Investigators will recruit 60 children to allow for 33% attrition. While the inclusion criteria are the same as other studies, here investigators do use spoken language exposure as a grouping variable, as follows: based on responses to the language background questionnaire regarding exposure to spoken English, participants will be grouped according to language use as monolingual ASL or bimodal bilingual (spoken English/ASL). Participants will be identified as bimodal bilingual is 1) the primary caregiver reports spoken English to communicate with their child (either alone or in conjunction with ASL), and 2) the primary caregiver reports that their child's ability to understand spoken English is at least a 3 on a Likert-type scale ranging from 0-5. Parents in this group will complete the short-form English CDI in addition to the ASL language measures.

Procedure: Participants will sit across a table from an experimenter who will present pairs of objects--one familiar, one novel--with one pair in each of nine trials (three per condition). The experimenter will prompt the participant to give them one of the toys, signing "I WANT YOU-GIVE-ME WHAT?" Then the experimenter will provide a cue; the child's selection will be recorded. In the gaze condition, the cue will be a gaze shift to the familiar object. In the mutual exclusivity condition, the cue will be a novel sign. In the conflict condition, both a gaze shift to the familiar object and a novel sign will be used. The trial order and object pair will be pseudo-randomly assigned.

Planned analysis: Investigators will use an omnibus mixed effects binomial model to determine how well condition and language environment predict the likelihood to select the novel object, with item and child as random factors.

Conditions
Deafness
Being tested
input cue
Keywords
deafness, American Sign Language
Medical subject headings
Deafness

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • input cueOther

    The object is labelled with 1) gaze only; 2) novel label only; or 3) conflicting gaze and novel label

Study groups in NCT05993832
Study groupRoleWhat they receive
Word learning from referential cuesExperimentalAll participants are provided pairs of objects (one familiar, one novel) with an accompanying prompt. The prompt types are 1) gaze (3 trials); 2) mutual exclusivity (3 trials); or 3) conflict (3 trials)
Receives: Other: input cue

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Novel Object Selected

    In each trial two objects are presented to the child, one novel and one familiar, along with one of three prompt types. Children select one of the two objects on the table in front of them by picking it up and handing it to the experimenter. One each trial, the selected object is scored as novel or familiar based on which object is selected. Data is analyzed as proportion of trials on which the novel object was selected.

    Measured: Trial time frame: 10 seconds, beginning from the end of the experimenter's prompt, i.e. once the experimenter asked the child for an object, the child had 10 seconds to respond by selecting one of the two presented objects.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Aug 2023
  2. Study start7 Aug 2023
  3. Primary completion20 Jun 2025
  4. Study completion20 Jun 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
48 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05993832
Sponsor's protocol ID
4067E
Other IDs
R01DC015272
Status last verified
Aug 2026
First submitted
7 Aug 2023
Last updated
15 Sep 2026
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Fitch A, Lieberman AM. Deaf Children's Use of Mutual Exclusivity and Eye Gaze to Determine Word Meanings in American Sign Language. Dev Sci. 2026 Sep;29(5):e70202. doi: 10.1111/desc.70202.

    PubMed 42374996

Questions about this trial

What is this clinical trial studying?

A study testing input cue in people with Deafness, run by Boston University Charles River Campus at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 15 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 15 Sep 2026). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Novel Object Selected (time frame: Trial time frame: 10 seconds, beginning from the end of the experimenter's prompt, i.e. once the experimenter asked the child for an object, the child had 10 seconds to respond by selecting one of the two presented objects.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05993832, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Sep 2026.

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