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AphasiaNCT07455162

Effects of Gesture Plus Verbal Treatment (GVT) in Cantonese Speakers With Aphasia

A study testing Verbal treatment and Gesture plus verbal treatment in people with Aphasia and Gestures, run by Hong Kong University at 1 site in Hong Kong.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This research aims to explore the relative efficacy of Verbal-only and GVT on naming difficulty in Cantonese-speaking people with aphasia (PWA). The primary research question in this study is: "For Cantonese-speaking people with aphasia, what are the relative effects of verbal treatment compared to gesture plus verbal… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Aphasia, Gestures
What is being tested?
Verbal treatment and Gesture plus verbal treatment
Could I receive a placebo?
No, everyone receives an active treatment
How many people
90 participants
Where
1 siteHong Kong
Study dates
1 Apr 2025to Sep 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Diagnosed with aphasia
  • Demonstrate Word finding Difficulty (WFD)
  • Able to repeat single words
  • Normal (or corrected) vision and hearing
  • Aphasia resulting from a unilateral left hemisphere stroke
  • Premorbidly fluent in spoken Cantonese
  • Without significant cognitive impairments
  • Chronic aphasia resulting from a unilateral left hemisphere stroke

Who cannot join

  • A history of other neurological disorders
  • With the above moderate to severe or severe motor speech impairment
  • With moderate to severe apraxia of speech
  • With very mild or very severe aphasia

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Hong Kong1 site, 1 recruiting
  • The University of Hong Kong

    Hong Kong

    Annie Zhiyao Hu, 852-6068-8312, annie920@connect.hku.hk

    Recruiting

Other trials in Hong Kong

About this study

Official title: Contrasting Effects of Verbal Treatment and Gesture Plus Verbal Treatment for Word Retrieval in Cantonese Speakers With Aphasia

This research aims to explore the relative efficacy of Verbal-only and GVT on naming difficulty in Cantonese-speaking people with aphasia (PWA).

The primary research question in this study is: "For Cantonese-speaking people with aphasia, what are the relative effects of verbal treatment compared to gesture plus verbal treatment (GVT) on verbal and gesture naming at different levels?"

People with aphasia will be engaged in a repeated measures experimental design. Participants will be engaged in two phases of training. In the first phase, participants will be assigned to receive verbal-only treatment. To minimize and prevent the carry-over effects caused by the first intervention, a one-month washout period will be implemented before the start of the second phase. After a washout period, participants will switch to GVT in the second phase.

Conditions
Aphasia, Gestures
Being tested
Verbal treatment, Gesture plus verbal treatment
Keywords
Aphasia, Gesture, Rehabilitation
Medical subject headings
Aphasia, Gestures

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Verbal treatmentBehavioural

    This study will involve the following naming interventions: 1) Semantic Features Analysis, 2) Modified Ortho-phonological cueing therapy and Phonological Component Analysis, and 3) Repetition with Cueing Hierarchy.

  • Gesture plus verbal treatmentBehavioural

    This study will involve the following interventions:

    1. Combined Semantic and Gesture treatment, 2) Combined Phonological and Gesture treatment, and 3) Combined Repetition and Gesture treatment.
Study groups in NCT07455162
Study groupRoleWhat they receive
Verbal-onlyActive comparatorThis is a within-subject comparison study where each participant receives both interventions sequentially. During the first phase, participants receive verbal-only therapy (VT). In the subsequent phase, they receive Gesture verbal treatment (GVT). The order of interventions is fixed, and each participant acts as their own control to compare the effects of the two interventions.
Receives: Behavioral: Verbal treatment
Gesture plus VerbalActive comparatorThis is a within-subject comparison study where each participant receives both interventions sequentially. During the first phase, participants receive verbal-only therapy (VT). In the subsequent phase, they receive Gesture verbal treatment (GVT). The order of interventions is fixed, and each participant acts as their own control to compare the effects of the two interventions.
Receives: Behavioral: Gesture plus verbal treatment

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Changes in the scores of the Naming Probes

    The treatment effects on naming will be assessed through verbal naming and gesture production using the black and white drawing naming task. Responses will be counted as correct if they can be identified by the rater as the target word in verbal naming and convey the depicted concept through gesture production, even if the articulation or hand and arm movements are slightly distorted.

    Measured: From enrollment to the end of treatment at 4 weeks

Secondary outcomes (5)
  1. Changes in the scores of the Cantonese Aphasia Battery

    The Cantonese Aphasia Battery was conducted to evaluate improvements in various linguistic measures (e.g., question comprehension, step commands, repetition, etc.). The minimum and maximum values are 0 and 100, respectively, with higher scores indicating a better outcome.

    Measured: From enrollment to the end of treatment at 4 weeks

  2. Changes in the scores of the Comprehensive Aphasia Test

    The Comprehensive Aphasia Test will be conducted to evaluate improvements in various cognitive and linguistic measures (e.g., semantic memory, word fluency, auditory comprehension, etc.). There are different subtests in the assessment, with a minimum value of 0, and maximum values ranging from 70 to 130, with higher scores indicating a better outcome.

    Measured: From enrollment to the end of treatment at 4 weeks

  3. Changes in the scores of the Cantonese Boston Naming Test

    The Cantonese Boston Naming Test will be conducted to evaluate the generalization effects on naming ability. The minimum and maximum values are 0 and 30, respectively, with higher scores indicating a better outcome.

    Measured: From enrollment to the end of treatment at 4 weeks

  4. Changes in the number of main concepts and gestures in discourse production tasks

    Discourse samples were collected from participants through various monologues. The discourse elicitation tasks included Main concept analysis, procedural (Ham and Egg Sandwich), narrative (Telling of the story "Tortoise and Hare"), and personal narrative (Sharing of an important event). This will help in assessing their word retrieval abilities at both the sentence and discourse levels, and their verbal and non-verbal communication skills in realistic contexts. Regarding discourse assessment, all samples will be video recorded using a camera. After that, the samples will undergo discourse analysis based on Chinese Linguistics Communication Measures, where conversational speech will be transcribed, and the linguistic index will be calculated and compared. Finally, the number of various types of gestures will also be computed and compared.

    Measured: From enrollment to the end of treatment at 4 weeks

  5. Changes in the scores of the Functional Communication questionnaire

    Improvements in functional communication will be evaluated using the Functional Assessment of Communication Skills questionnaire. There are different subtests in the assessment, with minimum values of 0, and maximum values ranging from 35 to 147, with higher scores indicating a better outcome.

    Measured: From enrollment to the end of treatment at 4 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Mar 2026
  2. Study start1 Apr 2025
  3. Primary completionSep 2028 (estimated)
  4. Study completionSep 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Sequential
Model description
Participants will be engaged in two phases of training. In the first phase, participants will be assigned to receive verbal-only treatment. To minimize and prevent the carry-over effects caused by the first intervention, a one-month washout period will be implemented before the start of the second phase. After a washout period, participants will switch to GVT in the second phase.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
90 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07455162
Sponsor's protocol ID
EA240609
Status last verified
Feb 2026
First submitted
24 Feb 2026
Last updated
11 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: According to the consent form approved by HREC, any information obtained in this study will remain strictly confidential (except as required by relevant legal authorities), and will be used for research purposes and clinical education use only. Videos, verbatim transcripts, and data will be uploaded to TalkBank Consortium (talkbank.org), allowing authorized researchers and educators from other institutions to view, analyze, and compare the data.

Publications

  • Yiu, E. M-L. (1992). Linguistic assessment of Chinese-speaking aphasics: Development of a Cantonese aphasia battery. Journal of Neurolinguistics, 7(4), 379-424. https://doi.org/10.1016/0911-6044(92)90025-R

  • Lau, S. W. -H. (2001). The Cantonese FACS feasibility with aphasic patients in Hong Kong. Unpublished bachelor dissertation, The University of Hong Kong, Hong Kong.

  • Kong, A. P.-H., & Wang, C. (2016). Main concept analysis (MCA) for oral discourse production. In. Hong Kong: The Commercial Press H.K Ltd.

  • Kong, A. P.-H., & Ng, C. Y.-T. (2022). Psycholinguistic Considerations for Adapting the Cantonese Version of Comprehensive Aphasia Test (Cant-CAT): A Feasibility Study. Perspectives of the ASHA Special Interest Groups, 7(4), 1211-1222. https://doi.org/doi:10.1044/2022_PERSP-22-00044

  • Kong AP, Law SP. A linguistic communication measure for monitoring changes in Chinese aphasic narrative production. Clin Linguist Phon. 2009 Apr;23(4):255-69. doi: 10.1080/02699200802673234.

    PubMed 19382013
  • Cheung RW, Cheung MC, Chan AS. Confrontation naming in Chinese patients with left, right or bilateral brain damage. J Int Neuropsychol Soc. 2004 Jan;10(1):46-53. doi: 10.1017/S1355617704101069.

    PubMed 14751006
  • Kong, A. P.-H., Hu, A. Z., Wong, C. C.-T., & Wong, C. W.-Y. (2025). Effects of modified word and sentence level gesture plus verbal treatment (GVT) in Cantonese speakers with aphasia. Aphasiology, 1-32. https://doi.org/10.1080/02687038.2025.2540297

Questions about this trial

What is this clinical trial studying?

A study testing Verbal treatment and Gesture plus verbal treatment in people with Aphasia and Gestures, run by Hong Kong University at 1 site in Hong Kong.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 11 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Annie Zhiyao Hu (852-6068-8312, annie920@connect.hku.hk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Changes in the scores of the Naming Probes (time frame: From enrollment to the end of treatment at 4 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07455162, which also lists 7 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Mar 2026.

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