A Study to Evaluate Intensive Dynamic Temporal and Tactile Cueing Treatment for Childhood Apraxia of Speech

Overview

About this study

The purpose of this study is to systematically examine components of the Dynamic Temporal and Tactile Cueing (DTTC) therapy when it is applied intensively (at high dosage).

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Documented diagnosis of childhood apraxia of speech.
  • Males and females; age 24 months – 12 years.
  • Intelligibility limitations impact communication success.
  • Informed assent and parental informed consent to participate in the study.
  • Parental willingness to comply with all study procedures and lifestyle considerations and availability for the duration of the study.
  • Ability to participate in two 30-minute therapy sessions 5 days per week.
  • Judged to display behavioral characteristics prerequisites for success with DTTC:
    • Ability and willingness to focus on the clinician’s face for at least two seconds;
    • Ability and willingness to attempt imitation of oral movements
    • Ability and willingness to follow simple directions;
    • Ability and willingness to perform 4 trials of the same speech target;
    • Receptive language within average range or mildly delayed as demonstrated by SS > 74 on a standardized test of language ability.

Exclusion Criteria:

For Experiment 1, an individual who meets any of the following criteria will be excluded from participation in this study:

  • Presence of cleft lip/palate.
  • Diagnosis of autism spectrum disorder.
  • Diagnosis of more than equivocal dysarthria.

For Experiment 2, these exclusion criteria do not apply.

Eligibility last updated 1/18/24 Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Heather Clark, Ph.D.

Closed-enrolling by invitation

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"Close"
Not open to everyone who meets the eligibility criteria, but only those invited to participate by the study team.

Contact information:

Iesha Abbajebel

(507) 422-9975

Abbajebel.Iesha@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20508313

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