Maximizing Language Development in Children With Hearing Loss
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|ClinicalTrials.gov Identifier: NCT01963468|
Recruitment Status : Completed
First Posted : October 16, 2013
Last Update Posted : March 29, 2018
|Condition or disease||Intervention/treatment||Phase|
|Hearing Loss||Behavioral: Early language intervention||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||20 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Pre-Implantation Communication Treatment for Children With Hearing Loss|
|Study Start Date :||October 2013|
|Actual Primary Completion Date :||December 2016|
|Actual Study Completion Date :||December 2016|
Experimental: Early language intervention
Children will receive 6 months of weekly parent-implemented intervention sessions.
Children will be assessed monthly via audio recordings and language checklists to monitor language development more closely.
Behavioral: Early language intervention
Parents will practice the specific set of strategies (visual, interactive, tactile, responsive) during sessions that occur weekly and last 1 hour for a total of 26 sessions, over 6 months. Each session will include four segments: (a) the therapist will review the intervention strategies taught in the workshop (10 min), (b) the therapist will model the intervention strategy with the child (10 min), (c) the parent will practice the strategy with her child with coaching from the therapist across four different routines and activities of the parent's choice (30 min), and (d) the therapist will provide feedback to the parent, summarize the session, and answer the parent's questions (10 min).
No Intervention: Monthly language check-ups
Children will be assessed monthly via home observations and parents will complete a language checklist to monitor language development more closely.
- MacArthur Communicative Development Inventories [ Time Frame: one month ]
- Preschool Language Scale [ Time Frame: 6 months ]
- Communication and Symbolic Behavior Scales [ Time Frame: 6 months ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01963468
|United States, Illinois|
|Evanston, Illinois, United States, 60202|
|Principal Investigator:||Megan Y Roberts, PhD, CCC-SLP||Northwestern University|