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NCT05916222: DTTC

The Effects of Caregiver Training on DTTC Treatment Outcomes in CAS

Recruiting now NA Last updated 20 January 2026
What this trial tests

NA trial testing Dynamic Temporal and Tactile Cueing (DTTC) in Childhood Apraxia of Speech in 40 participants. Currently enrolling.

Timeline
19 July 2023
Primary endpoint
30 May 2026
31 December 2026

Quick facts

Lead sponsorNew York University
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment40
Start date19 July 2023
Primary completion30 May 2026
Estimated completion31 December 2026
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

New York University

Who can join

Adults 24 Months to 95 Months, any sex, with Childhood Apraxia of Speech. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to investigate the impact of direct vs. indirect caregiver training on treatment outcomes following a period of Dynamic Temporal and Tactile Cueing (DTTC) intervention combined with home practice in childhood apraxia of speech (CAS). Forty children with CAS, between the ages of 2;5 and 7;11 years of age, will be recruited for this study. All children will receive DTTC treatment at the frequency of standard care (2x/week) in a university clinic over and 8-week period. Participants will be randomly assigned to one of two groups: the Direct Training Group; the Indirect Training Group. All caregivers will complete an educational module about CAS, will observe all sessions, and will engage in home practice with their children. Caregivers in the Direct Group will receive coaching in the use of DTTC with their child during a portion of each treatment session to support home practice, whereas those in the Indirect Group will not receive detailed guidance for home practice. Caregivers in both groups will practice at home with their children during the treatment phase (3x/week). Following the treatment phase, home practice will continue at a higher frequency (6x/week) during a 4-week follow-up phase. Treatment outcomes will be compared between groups.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Childhood Apraxia of Speech

Currently open trials in the same condition.

Other New York University trials

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Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing