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Behavioral Intervention
DTTC with Caregiver Training for Childhood Apraxia of Speech (DTTC Trial)
N/A
Recruiting
Research Sponsored by New York University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
2;6-7;11 years of age at the start of treatment
Primary speech diagnosis of Childhood Apraxia of Speech (CAS) based on auditory-perceptual, expert diagnosis and/or Dynamic Evaluation of Motor Speech Skills (DEMSS) score classification of 'significant evidence of CAS' with score <323
Must not have
Hearing impairment
Primary diagnosis of dysarthria or other speech sound disorder (e.g., phonological impairment)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up pre- to post-treatment (16 treatment sessions over 8 weeks); 1-week and 4-week post-treatment follow-up
Awards & highlights
No Placebo-Only Group
Summary
This trial tests which type of caregiver training helps children with childhood apraxia of speech improve their speaking abilities more effectively. Children receive specialized speech therapy and practice at home with their caregivers. The study aims to see which method leads to better speech accuracy and communication skills.
Who is the study for?
This trial is for children aged between 2 years and 5 months to 7 years and 11 months with a primary diagnosis of Childhood Apraxia of Speech (CAS) who speak English as their main language. Kids with autism, global developmental delay, Down syndrome, or severe hearing or visual impairments can't join. Those already receiving speech treatment elsewhere are also excluded.
What is being tested?
The study tests the effects of caregiver training on DTTC therapy outcomes in kids with CAS. Forty children will receive standard DTTC treatments twice weekly at a clinic over eight weeks. They'll be split into two groups: one gets direct coaching for home practice; the other doesn't.
What are the potential side effects?
Since this trial involves speech therapy techniques rather than medication, there aren't typical drug side effects. However, it's possible that participants may experience frustration or fatigue from intensive practice sessions.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am between 2 and 11 years old.
Select...
I have been diagnosed with Childhood Apraxia of Speech.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have hearing loss.
Select...
I have been diagnosed with a speech disorder.
Select...
I have abnormalities in the structure of my mouth.
Select...
My child's cognitive score is below 70, indicating a significant delay.
Select...
I have vision problems that glasses or contacts can't fix.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ pre- to post-treatment (16 treatment sessions over 8 weeks); 1-week and 4-week post-treatment follow-up
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~pre- to post-treatment (16 treatment sessions over 8 weeks); 1-week and 4-week post-treatment follow-up
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Changes in word accuracy
Secondary study objectives
Changes in phoneme accuracy
Changes in speech intelligibility
Changes in the FOCUS-34 score
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Direct Training (DTTC + Coaching + Home Practice)Experimental Treatment1 Intervention
Children in the Direct Training Arm will receive DTTC treatment 2x/week for 8 weeks with half of each session administered only by the SLP. In the other half of the session, DTTC will be administered by the parent/caregiver with online coaching by the SLP. During the coaching portion of treatment sessions, the SLP will provide direct training to guide the parent/caregiver in the administration of DTTC to support home practice sessions. Parent/caregivers in this Arm will also complete an online, self-paced educational module on CAS prior to the start of treatment and review home practice guidelines with the clinician at the end of each therapy session. Parent/caregivers will engage their children in home practice during the treatment phase and follow-up phase. Home practice will consist of 30-minute practice sessions 3x/week during the 8-week treatment phase and 6x/week during the 4-week follow-up phase.
Group II: Indirect Training (DTTC + Home Practice)Active Control1 Intervention
Children in the Indirect Training Arm will receive DTTC treatment 2x/week administered by an SLP for 8 weeks. Parent/caregivers in this Arm will complete an online, self-paced educational module on CAS prior to the start of treatment, observe all treatment sessions, and review home practice guidelines with the clinician at the end of each therapy session. Parent/caregivers will engage their children in home practice during the treatment phase and follow-up phase. Home practice will consist of 30-minute practice sessions 3x/week during the 8-week treatment phase and 6x/week during the 4-week follow-up phase.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Dynamic Temporal and Tactile Cueing (DTTC) is a common treatment for Childhood Apraxia of Speech (CAS) that focuses on improving speech motor planning and execution. It involves structured, repetitive practice with temporal and tactile cues, breaking down speech into smaller units and gradually increasing complexity.
Temporal cues help in timing speech movements, while tactile cues provide physical feedback for correct articulation. This method is essential for CAS patients as it directly addresses their impaired motor planning and coordination, leading to more accurate and consistent speech production.
HABIT+tDCS: a study protocol of a randomised controlled trial (RCT) investigating the synergistic efficacy of hand-arm bimanual intensive therapy (HABIT) plus targeted non-invasive brain stimulation to improve upper extremity function in school-age children with unilateral cerebral palsy.Bimanual Skill Learning after Transcranial Direct Current Stimulation in Children with Unilateral Cerebral Palsy: A Brief Report.Transcranial Direct Current Stimulation (tDCS) in Unilateral Cerebral Palsy: A Pilot Study of Motor Effect.
HABIT+tDCS: a study protocol of a randomised controlled trial (RCT) investigating the synergistic efficacy of hand-arm bimanual intensive therapy (HABIT) plus targeted non-invasive brain stimulation to improve upper extremity function in school-age children with unilateral cerebral palsy.Bimanual Skill Learning after Transcranial Direct Current Stimulation in Children with Unilateral Cerebral Palsy: A Brief Report.Transcranial Direct Current Stimulation (tDCS) in Unilateral Cerebral Palsy: A Pilot Study of Motor Effect.
Find a Location
Who is running the clinical trial?
Hofstra UniversityOTHER
5 Previous Clinical Trials
278 Total Patients Enrolled
New York UniversityLead Sponsor
240 Previous Clinical Trials
220,239 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am between 2 and 11 years old.I am not receiving speech therapy from another provider during this study, but I may be getting language or AAC therapy.I have hearing loss.I have been diagnosed with a speech disorder.I have abnormalities in the structure of my mouth.My child's cognitive score is below 70, indicating a significant delay.Your language test scores are lower than 70 on tests like REEL-4, CELF-P3, or CELF-5.I have vision problems that glasses or contacts can't fix.I have a condition like autism, Down syndrome, or similar, but can focus in sessions with help.I have been diagnosed with Childhood Apraxia of Speech.
Research Study Groups:
This trial has the following groups:- Group 1: Direct Training (DTTC + Coaching + Home Practice)
- Group 2: Indirect Training (DTTC + Home Practice)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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