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Developmental Language DisorderTime2LearnNCT05901493

Category Learning Retention in Adults With and Without Developmental Language Disorder

A study testing Perceptual category training in people with Developmental Language Disorder and Adults Without Language Disorder, run by University of Delaware at 2 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Approximately 7% of the population experiences developmental language disorder (DLD), a language disorder with unclear causes. DLD affects communication beyond adolescence and poses challenges for education and career advancement due to difficulties in learning and memory. Read more about this study

Who is it for?
Ages 18 to 55 yearsHealthy volunteers can take part
What is being tested?
Perceptual category training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
540 participants
Where
2 sitesUnited States
Study dates
23 Oct 2022to 31 Jul 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

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 55 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • native speakers of American English
  • Grew up in a household in which only American English was spoken
  • 18-55 years of age
  • Typical vision \& hearing
  • (Aim 2) access to headphones/devices capable of accessing experiment script via internet
  • Must meet criteria for Group membership as either TD or DLD

Who cannot join

  • History of neurological disorders
  • History of psychiatric disorders
  • History of socio-emotional disorders
  • On prescription medication(s) that alter sleep

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Frances Earle, PhD contact

6468128376

fsearle@udel.edu

United States2 sites, 2 recruiting
  • Northeastern University

    Boston, Massachusetts, 02115

    Zhenghan Qi, PhD, z.qi@northeastern.edu

    Recruiting
  • University of Delaware

    Newark, Delaware, 19713

    Frances S Earle, PhD, 302-831-3878, fsearle@udel.edu

    Recruiting

Other trials in United States

About this study

Official title: Improving the Retention of Speech-Perceptual Learning in Adults With and Without Language Disorder

Approximately 7% of the population experiences developmental language disorder (DLD), a language disorder with unclear causes. DLD affects communication beyond adolescence and poses challenges for education and career advancement due to difficulties in learning and memory. Recent research suggests that adults with DLD struggle with overnight memory consolidation, indicating a need for effective learning and memory support. This project aims to determine the optimal training schedule for perceptual memory retention in adults with and without DLD. The study involves recruiting 240 adults (120 with DLD, 120 without) for speech-perceptual training with different training schedules. The researchers predict that the manipulation of training schedules will interact with circadian preference and overnight consolidation, leading to the discovery of the best practice schedule for speech sound retention. Additionally, 300 more adults (150 with DLD, 150 without) will be recruited to investigate how optimal training schedules interact with reflexive and reflective learning strategies. The time course of learning and retention will be tracked during reflexive and reflective categorization training in six different training schedules.

Read the detailed description

Developmental language disorder (DLD) describes the idiopathic disorder(s) of language that occurs in approximately 7% of the population. Although DLD is understudied in adulthood, it is clear that the communication challenges in DLD extend beyond adolescence. The barriers to educational and vocational achievement for adults with DLD include persistent difficulties in learning and memory. Recent work suggests that these difficulties with learning and memory include deficits in overnight memory consolidation. Thus, an effective support for learning and memory function in adults with DLD must include strategies for both overcoming initial challenges in learning, as well as in mitigating a deficit in consolidation of learned information. In this project, the investigators combine insights from the neurobiology of learning and memory, chronobiology, and speech perception, to determine the optimal training schedule for perceptual memory retention in adults with and without DLD. The investigators have two Aims in this project: First, the investigators will recruit 240 adults (120 with/120 without DLD) to participate in a speech-perceptual training to take place in one of six different training schedules over 24 hours. The investigators predict that our manipulation of training schedules will interact with circadian preference and timing relative to overnight consolidation, to allow the discovery of the optimal practice schedule for speech sound retention for adult learners with \& without DLD. Under our second aim, the investigators will recruit an additional 300 adults (150 with/150 without DLD) in order to determine how optimal training schedules interact with reflexive and reflective learning strategies in adults with and without DLD. The investigators will achieve this aim by tracking the time course of learning and retention in adults participating in reflexive and reflective categorization training in one of six training schedules.

Being tested
Perceptual category training
Medical subject headings
Language Development Disorders

What participants receive

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

  • Perceptual category trainingBehavioural

    Participants complete a forced-choice categorization task with feedback, in order to learn difficult auditory and visual categories

Study groups in NCT05901493
Study groupRoleWhat they receive
Blocked Evening Only TrainingExperimentalOne hour training in the evening, followed by a one hour training 24 hours later
Receives: Behavioral: Perceptual category training
Distributed Evening TrainingExperimentalOne hour training in the evening, followed by a two 30 min trainings 12 and 24 hours later
Receives: Behavioral: Perceptual category training
Blocked Evening-Morning TrainingExperimentalOne hour training in the evening, followed by a one hour training 12 hours later
Receives: Behavioral: Perceptual category training
Blocked Morning Only TrainingExperimentalOne hour training in the morning, followed by a one hour training 24 hours later
Receives: Behavioral: Perceptual category training
Distributed Morning TrainingExperimentalOne hour training in the morning, followed by a two 30 min trainings 12 and 24 hours later
Receives: Behavioral: Perceptual category training
Blocked Morning-Evening TrainingExperimentalOne hour training in the morning, followed by a one hour training 12 hours later
Receives: Behavioral: Perceptual category training

What is being measured

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

  1. Speech discrimination - behavior

    Participants will be administered a short (approximately 4-minute) behavioral task. They will be exposed to two speech sounds, separated by a 1-second interval. Some sounds will begin with the dental stop consonant, and other sounds will begin with the retroflex stop consonant. Participants will be asked to decide if the two sounds they hear are the same or different. Accuracy will be converted to d-prime (a measure of signal detection). This d-prime score will be the primary behavioral outcome for speech discrimination.

    Measured: 1 week

  2. category identification - behavior

    Participants will be administered a short (approximately 2 minutes) for each modality (auditory and visual). Participants will either hear (auditory - pure tone) or see (visual - gabor patch) a stimulus, and will need to choose which category the stimulus belongs to out of a choice of two. The percentage of trials that are answered correctly will be the primary behavioral outcome for auditory and visual category identification.

    Measured: 48 hours

Secondary outcomes (1)
  1. Speech discrimination - Event-related potential of the electroencephalogram (ERP/EEG)

    The investigators will fit the participant's head with a pre-positioned electrode cap, with electrolytic gel applied between the electrodes and the scalp. The participants will watch a silent movie while dental and retroflex speech tokens are presented in an oddball paradigm. The investigators will record the participants' electroencephalogram (EEG) while the auditory stimuli are presented. The EEG data will be segmented to examine the fluctuations in voltage recorded at the scalp (in milivolts) for a duration of one second after the onset of each stimulus. The segmented data will be averaged across dental trials, and across the retroflex trials. The resultant waveforms will be subtracted from one another. The peak of the deflection in the difference waveform found approximately 250miliseconds following stimulus onset is the mismatch negativity (MMN) component. The magnitude of the MMN component will be our primary outcome measure.

    Measured: 1 event-related potential (ERP) session 1 week following training

Timeline

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

  1. First posted13 Jun 2023
  2. Study start23 Oct 2022
  3. Primary completion31 Dec 2026 (estimated)
  4. Study completion31 Jul 2027 (estimated)

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
Randomised
Intervention model
Parallel groups
Model description
Participants will be assigned to one of six training schedules to complete over 48 hours. All participants will complete the same amount of training. The investigators will examine retention of trained information at the end of the week.
Masking
None (open label)
Enrolment
540 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05901493
Sponsor's protocol ID
1938428
Acronym
Time2Learn
Status last verified
May 2026
First submitted
19 May 2023
Last updated
29 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: de-identified data will be uploaded to the Open Science Framework alongside publications to stem from data from this project

Questions about this trial

What is this clinical trial studying?

A study testing Perceptual category training in people with Developmental Language Disorder and Adults Without Language Disorder, run by University of Delaware at 2 sites 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 6 inclusion and 4 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: looking for participants now, as of the sponsor's last update on 29 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Frances Earle, PhD (6468128376, fsearle@udel.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Speech discrimination - behavior (time frame: 1 week). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 29 May 2026.

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