CClinicalTrials.gg
CompletedNCT02545894Updated Jan 29, 2020

An Evaluation of a New Nonverbal Treatment for Global Aphasia

An interventional study of Cognitive therapy in Stroke, sponsored by University College, London. Completed at 1 site in United Kingdom. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-01-29.

Sponsored by University College, London · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Dec 2014, registered Jun 2015).
Phase
Not applicable
Study type
Interventional
Enrollment
6
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

People with global aphasia (PwGA) post stroke have little to no meaningful communication abilities (ie limited comprehension, spoken language, reading and writing abilities).A proportion of PwGA will also have limited abilities to use any alternative means of communication e.g. gesture, pictures or computer devices. There is a suggestion in the literature that this is because of co-occurring cognitive deficits. The consequence is that these clients are unable to reliably communicate even their basic needs.This is commonly known as having no functional communication abilities. Such PwGA tend not to respond to standard speech and language therapy interventions.

This research will investigate the effect of a new cognitive intervention designed to improve basic functional communication abilities. The treatment will be nonverbal and involve computer and paperbased tasks ordered hierarchically from basic to more complex tasks. Six to eight participants will take part. All their sessions will take place in their own home. For some this may be a care home. They will first complete a diagnostic communication assessment in order for baseline abilities to be established. Further formal language and cognitive assessments will be conducted over a period of 6 weeks. A relative/friend will complete a questionnaires about mood/communication. The PwGA will also be videoed interacting with the research student e.g. looking at a magazine, completing a jigsaw, answering questions and making choices non-verbally.

The participants then receive the new intervention 3 times a week for 6 consecutive weeks. All intervention sessions will be videoed. Then participants will be reassessed over 2 weeks using the same assessments as prior to the intervention. The questionnaire with their relative/friend and videoed activity session will also be repeated. After a twelve week break the participant will be videoed interacting with the research student complete some of the assessments again and their relative will re-complete the questionnaires.

02

Conditions studied

  • Stroke

Browse trials for

03

In context

Aphasia

365 studies on the registry are indexed under Aphasia; 89 are open to participants now.

This study's enrollment of 6 is below the median of 30 across 316 interventional studies indexed under Aphasia.

Browse Aphasia studies →

Lead sponsor

University College, London is the lead sponsor of 632 studies on the registry; 145 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 2 (33%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • have global aphasia as diagnosed by an SLT
  • have little or no verbal output
  • inconsistent single word comprehension
  • little or no ability to read or write
  • little or no ability to use alternative modes of communication
  • Little or no ability to make choices in function
  • no diagnosis/history of a progressive neurological condition
  • no diagnosis of hearing loss
  • no diagnosis/history of a mental health condition
  • English as a first language

Exclusion criteria

Exclusion Criteria:

  • has another form of aphasia
  • is able to consistently express basic needs non-verbally or verbally.
  • is able to participate in communicative interaction with a familiar other
  • has a history of a progressive neurological condition
  • has hearing loss
  • has a diagnosis/history of a mental health condition
  • does not have English as a first language.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
6 participants (actual)

Study arms

  • No intervention
    BASELINE TESTING

    Language and cognitive assessments conducted

  • Experimental
    Treatment

    Intervention given: visual tracking pressing a button every time a picture is seen on the screen * playing dominoes and snap * pressing a button every time a specific picture is seen on the screen * Pressing a button every time a specific sound is heard * Matching objects to a picture * Matching gestures to objects * Matching two connected objects * Sorting objects by categories * Matching sounds to objects * "Complete the category" and "odd on out with objects" * Choosing target objects by pointing * Choosing objects to complete the category by pointing

    Behavioral: Cognitive therapy

  • No intervention
    Post intervention

    Repeated testing

Interventions

  • BehavioralCognitive therapy

    The tasks are: * visually tracking a picture as it moves across the computer screen * pressing a button every time a picture is seen on the screen * pressing a button every time a specific picture is seen on the screen * Pressing a button every time a specific sound is heard * Matching objects to a picture * Matching gestures to objects * Matching two connected objects * Sorting objects by categories * Matching sounds to objects * "Complete the category" and "odd on out with objects" * Choosing target objects by pointing * Choosing objects to complete the category by pointing

06

What researchers measure

Primary outcomes

  1. American Speech and Hearing Association -Functional Assessment of Communication

    Questionnaire completed by friend/relative

    Time frame: 27 weeks

  2. Constructed Interaction Task

    video recorded interaction

    Time frame: 27 weeks

Secondary outcomes

  1. Aphasia Screening Test

    Language assessment

    Time frame: 14 weeks

  2. Mood Screen

    depression screening tool

    Time frame: 27 weeks

  3. Pyramids and Palm Trees Test

    pictorial semantic assessment

    Time frame: 27 weeks

  4. Wisconsin Card Sorting Test

    cognitive assessment

    Time frame: 14 weeks

  5. Butt Non verbal reasoning test

    cognitive assessment

    Time frame: 27 weeks

  6. Western Aphasia Battery cognitive sub test

    cognitive assessment

    Time frame: 14 weeks

07

Study locations

1 site
  • University College London, Research Dept of Language and Cognition
    London, WC1N, United Kingdom
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 29, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02545894
Lead sponsor
University College, London
Responsible party
Sponsor
First posted
Sep 10, 2015
Start date
Dec 2014
Primary completion
Jun 2016
Completion
Dec 2016
Last update
Jan 29, 2020

Study contacts

Suzanne Beeke, PhD
principal investigator · UCL
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2020. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion