Literature DB >> 29635427

Caregiver-Reported Indicators of Communication and Social Functioning for Young Children Who Are Deaf or Hard of Hearing.

Donald L Patrick1, Todd C Edwards1, Poorna Kushalnagar2, Tari Topolski1, Brenda Schick3, Ann Skalicky4, Kathleen Sie5.   

Abstract

We elicited caregiver-reported observations of children aged 5-10 who were deaf or hard of hearing (DHH) that resulted in two age-specific instruments: Caregiver Report of Behaviors and Events (CROBE-DHH 5-7 and 8-10). These new instruments record observations on communication and social behaviors/events. In Study 1, 36 caregivers provided qualitative data on important content on what they were able to observe for instrument development and in Study 2, 271 provided data for studying cross-sectional measurement properties. Two modules resulted in 11 items for children age 5-7 and 15 items for children 8-10 years. Items showing good 7-day reproducibility (ICC over .70) and fair 4-week reproducibility (ICC over .50) were retained. Children with milder hearing loss received higher (better) scores. Items did not distinguish between those with or without cochlear implants. Analyses suggest that the instruments are best used as individual indicator items. In both age groups, caregivers reported youths missed out on family conversations and spent little time on their own. These content-validated indicators apply to all children with DHH. Further work will evaluate the usefulness of these indicators in evaluating change in communication and social behaviors, and the implications of results for intervention.

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Mesh:

Year:  2018        PMID: 29635427      PMCID: PMC5995206          DOI: 10.1093/deafed/eny006

Source DB:  PubMed          Journal:  J Deaf Stud Deaf Educ        ISSN: 1081-4159


  18 in total

1.  Adolescent quality of life, part I: conceptual and measurement model.

Authors:  Todd C Edwards; Colleen E Huebner; Frederick A Connell; Donald L Patrick
Journal:  J Adolesc       Date:  2002-06

Review 2.  Characteristics of health-related self-report measures for children aged three to eight years: a review of the literature.

Authors:  Joanne Cremeens; Christine Eiser; Mark Blades
Journal:  Qual Life Res       Date:  2006-05       Impact factor: 4.147

3.  Quality of life in youth with severe to profound sensorineural hearing loss.

Authors:  Abby Meyer; Kathleen Sie; Anne Skalicky; Todd C Edwards; Brenda Schick; John Niparko; Donald L Patrick
Journal:  JAMA Otolaryngol Head Neck Surg       Date:  2013-03       Impact factor: 6.223

Review 4.  Mental health of deaf people.

Authors:  Johannes Fellinger; Daniel Holzinger; Robert Pollard
Journal:  Lancet       Date:  2012-03-17       Impact factor: 79.321

5.  Quality of life in children and adolescents with cochlear implants and additional needs.

Authors:  Lindsey Edwards; Tina Hill; Merle Mahon
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2012-03-22       Impact factor: 1.675

6.  School placement and perceived quality of life in youth who are deaf or hard of hearing.

Authors:  Brenda Schick; Anne Skalicky; Todd Edwards; Poorna Kushalnagar; Tari Topolski; Donald Patrick
Journal:  J Deaf Stud Deaf Educ       Date:  2012-11-26

7.  Identifying infants with hearing loss - United States, 1999-2007.

Authors: 
Journal:  MMWR Morb Mortal Wkly Rep       Date:  2010-03-05       Impact factor: 17.586

8.  Resilience factors associated with adaptation in families with deaf and hard of hearing children.

Authors:  Ingrid A Ahlert; Abraham P Greeff
Journal:  Am Ann Deaf       Date:  2012

Review 9.  Assessment of health-related quality of life in children: a review of conceptual, methodological, and regulatory issues.

Authors:  Louis S Matza; Andrine R Swensen; Emuella M Flood; Kristina Secnik; Nancy Kline Leidy
Journal:  Value Health       Date:  2004 Jan-Feb       Impact factor: 5.725

Review 10.  The epidemiology of hearing impairment in the United States: newborns, children, and adolescents.

Authors:  Saral Mehra; Roland D Eavey; Donald G Keamy
Journal:  Otolaryngol Head Neck Surg       Date:  2009-04       Impact factor: 3.497

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  1 in total

1.  Exploration of Caregiver Interrater Agreement and Test-Retest Reliability on the Infant Cleft Observer Outcomes (iCOO).

Authors:  Salene M W Jones; Todd C Edwards; Brian G Leroux; Kathleen A Kapp-Simon; Donald L Patrick; Laura P Stueckle; Janine M Rosenberg; Meredith Albert; Claudia Crilly Bellucci; Cassandra L Aspinall; Katherine Vick; Carrie L Heike
Journal:  Cleft Palate Craniofac J       Date:  2022-03-28
  1 in total

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