- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04161573
Irony Comprehension Ability of Chinese Speaking Patients With TBI
November 10, 2019 updated by: National Taiwan University Hospital
A Preliminary Study on Irony Comprehension Ability of Chinese Speaking Patients With Traumatic Brain Injury
This study aims at understanding irony comprehension ability of Chinese speaking patients with TBI through a series of self-made stories.
Each story contains two characters having a conversation, and one of them would give a figurative (which is, ironic) or literal statement at the end of the story.
The participants are asked to figure out its meaning.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
The investigator plans to recruit TBI patients and control group whose gender and age accord with them, 15 people in each group.
They would be asked to read the materials mentioned above displaying by a computer.
It may take 30 minutes per time, and every participants only do once.
Study Type
Observational
Enrollment (Anticipated)
120
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Hsin-Tzu Tseng
- Phone Number: +886 978108036
- Email: s0480052@gmail.com
Study Locations
-
-
-
Taipei, Taiwan, 802
- Recruiting
- National Taiwan University Hospital
-
Contact:
- Hsin-Tzu Tseng
- Phone Number: +886 978108036
- Email: s0480052@gmail.com
-
-
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
20 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
NTUH
Description
Inclusion Criteria:
- Above 20 years old
- Chinese speaking people
- Diagnosed as TBI patients for over 6 months
- Having no other neurological and mental related problems
- Able to read with or without assistive device like glasses
Exclusion Criteria:
- Addicted to alcohol or drug morbid and postmorbid
- Having any communication disorders
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 |
Intervention / Treatment |
---|---|
TBI group
15 people in this group.
Each should be post TBI for 6 months.
|
All the participants would be asked to watch a series of self-made stories which are figurative or literal.
They have to figure out what is the real meaning of the character's statement.
The whole procedure will be done with a computer.
|
Control group to TBI
15 people in this group.
Their gender and age accord with TBI group.
|
All the participants would be asked to watch a series of self-made stories which are figurative or literal.
They have to figure out what is the real meaning of the character's statement.
The whole procedure will be done with a computer.
|
Aging group 1- 20 to 39
Normal people whose age range from 20 to 39.
|
All the participants would be asked to watch a series of self-made stories which are figurative or literal.
They have to figure out what is the real meaning of the character's statement.
The whole procedure will be done with a computer.
|
Aging group 2- 40 to 59
Normal people whose age range from 40 to 59.
|
All the participants would be asked to watch a series of self-made stories which are figurative or literal.
They have to figure out what is the real meaning of the character's statement.
The whole procedure will be done with a computer.
|
Aging group 3- above 60
Normal people whose age are above 60.
|
All the participants would be asked to watch a series of self-made stories which are figurative or literal.
They have to figure out what is the real meaning of the character's statement.
The whole procedure will be done with a computer.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
TBI group gets lower scores
Time Frame: 2 months
|
We assume that TBI group can't comprehend ironic statement as well as their control group.
Therefore, they may get lower score than their normal- health control group.
|
2 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: Yu-Chun Chih, PhD, Chung Shan Medical University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Angeleri R, Bosco FM, Zettin M, Sacco K, Colle L, Bara BG. Communicative impairment in traumatic brain injury: a complete pragmatic assessment. Brain Lang. 2008 Dec;107(3):229-45. doi: 10.1016/j.bandl.2008.01.002. Epub 2008 Feb 11.
- Carlomagno S, Giannotti S, Vorano L, Marini A. Discourse information content in non-aphasic adults with brain injury: a pilot study. Brain Inj. 2011;25(10):1010-8. doi: 10.3109/02699052.2011.605097.
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)
October 10, 2019
Primary Completion (ANTICIPATED)
December 31, 2019
Study Completion (ANTICIPATED)
January 31, 2020
Study Registration Dates
First Submitted
November 10, 2019
First Submitted That Met QC Criteria
November 10, 2019
First Posted (ACTUAL)
November 13, 2019
Study Record Updates
Last Update Posted (ACTUAL)
November 13, 2019
Last Update Submitted That Met QC Criteria
November 10, 2019
Last Verified
October 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201908029RINA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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