- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05697549
Effects of Cognitive Behavior Language Therapy for Patients With Post Stroke Aphasia
This study is clinical trial based and the target population in this study is patients with post-stroke aphasia. Cognitive linguistic quick test (CLQT) and Speech Language unhelpful thoughts and belief scale (SLUTBS) will apply as an assessment. Inclusive criteria include diagnosed male and female post-stroke severe aphasia patients above 30 years of age. These participants must have high instance of unhelpful speech language thoughts and belief. Participants in inclusive criteria must not be participated in any other psychotherapy/ speech language intervention program. Participants must sign an informed consent form. Participants having a caregiver who is willing to be present during the period of intervention. Exclusive criteria include individuals below 30 years of age and patients with aphasia caused by non-stroke etiology.
The aim of the study is to check the effects of cognitive behavior language therapy on patients with post-stroke aphasia. So, it will help speech language pathologists to adopt the principles of CBLT intervention to treat aphasia that occurs as a result of aphasia.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Punjab
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Rahim yar khan, Punjab, Pakistan
- Sheikh Zaid
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Both male and female.
- Over 30 years of age.
- All types of diagnosed aphasia.
- Severe aphasia following stroke.
- High instance of unhelpful speech language thoughts and belief.
- Participants who are not participating in any other psychotherapy / speech language intervention program will be included.
- Participants who are willing to sign an informed consent form.
- Participants having a caregiver who is willing to be present during the period of intervention.
Exclusion Criteria:
- Below 30 years of age.
- Patients with aphasia caused by a non-stroke etiology.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: cognitive behavior language therapy
Cognitive behavior language therapy is an extensive form of CBT.
And it is focused on the treatment of speech-language related problems.
CBLT helped the individuals to change their unhelpful thoughts and beliefs that cause difficulty for them to communicate properly and effectively.
The main aim of CBLT is to use their remaining language abilities, to restore their language abilities and to learn the other ways of communication i.e. pointing, gesturing and AAC.
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Cognitive behavior language therapy is an extensive form of Cognitive behavior therapy.
and it is used in the management of speech-language related problems.
It helps the individuals to change their unhelpful thoughts and beliefs that cause difficulty for them to communicate properly and effectively.
and it also helps the individuals to use their remaining language abilities, to restore their language abilities and to learn the other ways of communication i.e. pointing, gesturing and Augmentative alternative communication.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cognitive linguistic quick test
Time Frame: 4 week
|
scoring 3.5 to 4 indicates attention, memory, executive functions, language, visuospatial skills are within the normal limit.
whereas scoring 1 to 1.4 indicates that individual has severely affected in these areas.
|
4 week
|
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Speech language and helpful thoughts and belief scale
Time Frame: 4 week
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the scoring of this scale according to 4. Likert scale.
In which ''4'' strongly agree indicates high communication gap while sharing thoughts with others and ''1'' strongly disagree indicates individuals haven't facing any difficulties while sharing thoughts.
|
4 week
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Aleena Irum, MSLP, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- aleena1irum
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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