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

Detailed Description

This study aims to:

  1. 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.

  2. 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.
  3. 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

    • Flanders
      • Leuven, Flanders, Belgium
        • KULeuven
    • Vlaams-Brabant
      • Leuven, Vlaams-Brabant, Belgium, 3000
        • Katholieke Universiteit Leuven
      • Leuven, Vlaams-Brabant, Belgium, 3000
        • KULeuven

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
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

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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