- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04500340
Effectiveness of Cognitive Behavioral Therapy of Reduction of Test Anxiety (GroupCBT)
August 4, 2020 updated by: Khem Raj Bhatta, University Grants Commission
Test Anxiety: Pervasiveness, Link With Academic Achievement and Impact of Cognitive-behavioral Intervention in Its Reduction
This study will evaluate the role of Group Cognitive Behavioral Therapy in test anxiety.
The study participants will be psychology undergraduates with social work and psychology majors.
The students will be selected among those who score three or more in Westside Test Anxiety Scale will participate in the study.
Westside Test Anxiety will be used two weeks after completion of the group Cognitive Behavioral Therapy protocol (Flaxman, Bond & Keogh.
2004).
The result will be analyzed using the t-test and Cohen's d.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
80
Phase
- Not Applicable
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
-
-
Bagmati
-
Kathmandu, Bagmati, Nepal
- Nepal Mega College and K and K International College
-
-
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
Description
Inclusion Criteria:
- Those Studying Social work and Psychology as Major subjects, Those who have scored 3 and above in Westside Test Anxiety scale
Exclusion Criteria:
- Those scoring below 3 in Westside Test Anxiety Scale
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
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group Cognitive Behavioral Therapy (Group CBT)
Intervention Group will receive ten-session group CBT for test anxiety.
Two sessions will be carried out each week.
|
The cognitive-behavioral therapy protocol developed by Flaxman, Bond & Keogh (2004) will be used as the intervention protocol.
This protocol consists of 10 Sessions which are provided twice a week (each group will have 10 students).
|
|
No Intervention: Control Group
The Control group will be waiting for the control group who will receive intervention if they demand after final assessment for outcome measure.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Westside Test Anxiety Scale (WTAS)
Time Frame: Change from Baseline Test Anxiety Scores after completion of Group Cognitive Behavioral Therapy ( after one and half month)
|
The WTAS consists of 10 items, each using a Likert response scale where 1= "Never true" and 5= "always true.
Total score is divided by 10 to obtain final scores.
The total score ranges from one to five.
Score of 1-2.9 is considered normal test anxiety and score of 3-5 is labelled as high test anxiety.
|
Change from Baseline Test Anxiety Scores after completion of Group Cognitive Behavioral Therapy ( after one and half month)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Khem R. Bhatta, Master, Tribhuvan University
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)
February 20, 2019
Primary Completion (Actual)
July 1, 2019
Study Completion (Actual)
July 1, 2019
Study Registration Dates
First Submitted
July 18, 2020
First Submitted That Met QC Criteria
August 4, 2020
First Posted (Actual)
August 5, 2020
Study Record Updates
Last Update Posted (Actual)
August 5, 2020
Last Update Submitted That Met QC Criteria
August 4, 2020
Last Verified
August 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- UGrantsCommission
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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