- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02099773
Support Staff-client Interactions With Augmentative and Alternative Communication
December 7, 2017 updated by: Universitaire Ziekenhuizen KU Leuven
Support Staff's Interactions With Adults With Intellectual Disability Who Use Augmentative and Alternative Communication
This exploratory and observational study focuses on adults with an intellectual disability (ID) and their support workers.
Two groups of clients are observed: clients using Key Word Signing, and clients using aided Augmentative and Alternative Communication (AAC).
Approximately half of adults with ID is estimated to experience communication difficulties.
AAC supports them in their daily communication aiming at optimal participation in society.
Current communication models, such as Participation Model (Beukelman & Mirenda, 2005) and International Classification of Functioning, Disability and Health (WHO, 2001), regard both client-related and environmental factors as important elements of communication.
A substantial part of the environmental factors is made up of the communication partners' characteristics.
In daycare and residential services for adults with ID the support worker is an important communication partner .
Study Overview
Status
Completed
Conditions
Detailed Description
This study aims to:
with regard to teaching Key Word Signing (KWS), a specific form of AAC, to support workers:
Analyse the relation between training method, support workers' attitude, and short and long term sign knowledge.
with regard to the use of manual signs in everyday communication between support workers and adults with ID:
- Identity the support workers' characteristics that may influence the quality/quantity of the communication between adults with ID who use manual signs and their support worker.
- Analyse the nature of this influence as well as any possible interaction effects with the clients' characteristics.
- Assess whether an existing instrument, designed for measuring interactions between parents and children with cerebral palsy using AAC, may be used with adults client and support workers.
Study Type
Observational
Enrollment (Actual)
40
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Flanders
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Leuven, Flanders, Belgium
- KULeuven
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Vlaams-Brabant
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Leuven, Vlaams-Brabant, Belgium, 3000
- Katholieke Universiteit Leuven
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Leuven, Vlaams-Brabant, Belgium, 3000
- KULeuven
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Support workers who work in residential facilities or day-centres for adults with intellectual disability, in Flanders.
Description
Inclusion Criteria:
- uses AAC with client
- client has congenital intellectual disability
- supports client for at least 6 months
Exclusion Criteria:
- client has dementia symptoms
- client has severe, non-corrected visual impairment
- client has diagnosed autism
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
support workers & AAC users
Support workers who use KeyWordSigning in the communication with their client who has an intellectual disability
|
support workers & KWS users
Support workers who use aided AAC in the communication with their client who has an intellectual disability
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Signing rate of support workers and individuals with intellectual disabilities
Time Frame: Three observation sessions over period of 2 weeks per participant, 2 years for all participants
|
Proportion: number of signed utterances divided by total number (spoken + exclusively spoken) of utterances
|
Three observation sessions over period of 2 weeks per participant, 2 years for all participants
|
Sign imitation rate support workers and individuals with intellectual disabilities
Time Frame: Three observation sessions over period of 2 weeks per participant, 2 years for all participants
|
Proportion: number of manual sign imitations divided by total number manual signs produced
|
Three observation sessions over period of 2 weeks per participant, 2 years for all participants
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Explicit Attitude of direct care staff towards manual signs
Time Frame: One testing per participant, over period of 6 months for all participants
|
Self-developed survey with subscales (Likert response): scaled score
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One testing per participant, over period of 6 months for all participants
|
Implicit Attitude of direct care staff working in towards manual signs
Time Frame: One testing per participant, over period of 6 months for all participants
|
Single-Category Implicit Association Test scores
|
One testing per participant, over period of 6 months for all participants
|
Communicative functions of individuals with intellectual disabilities
Time Frame: Three observation sessions over period of 2 weeks per participant, 2 years for all participants
|
Proportion of responses/acknowledgement versus all communicative functions (responses/acknowledgements as well as initiations)
|
Three observation sessions over period of 2 weeks per participant, 2 years for all participants
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Ellen Rombouts, PhD cand., KU Leuven
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 1, 2014
Primary Completion (Actual)
December 1, 2016
Study Completion (Actual)
May 1, 2017
Study Registration Dates
First Submitted
March 24, 2014
First Submitted That Met QC Criteria
March 26, 2014
First Posted (Estimate)
March 31, 2014
Study Record Updates
Last Update Posted (Actual)
December 11, 2017
Last Update Submitted That Met QC Criteria
December 7, 2017
Last Verified
November 1, 2017
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- S56517
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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