- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06024083
Skills Video Intervention for Chinese/Chinese Americans
March 20, 2024 updated by: Shireen L. Rizvi, PhD, ABPP, Rutgers, The State University of New Jersey
Dialectical Behavior Therapy Skills Video Intervention for Chinese and Chinese American College Students
This is a study that aims to test a coping skills intervention delivered via brief animated videos for Chinese and Chinese American college students.
Study Overview
Status
Recruiting
Intervention / Treatment
Detailed Description
We are interested in seeing whether a brief video-based Dialectical Behavior Therapy skills training intervention that incorporates Western psychotherapy components and Eastern philosophies would be perceived as relevant and useful for this culturally unique yet diverse group.
During the study, participants will (1) complete a 20-min online baseline questionnaire; (2) complete a brief survey each day using a phone App for up to four weeks; and may (3) receive a video each day during the intervention.
Study Type
Interventional
Enrollment (Estimated)
150
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 Contact
- Name: Shireen Rizvi, Ph.D
- Phone Number: 848-445-3914
- Email: slrizvi@gsapp.rutgers.edu
Study Contact Backup
- Name: Qingqing Yin, M.S.
- Phone Number: 732-630-8690
- Email: qy93@rutgers.edu
Study Locations
-
-
New Jersey
-
Piscataway, New Jersey, United States, 08854
- Recruiting
- Rutgers University
-
Contact:
- Shireen Rizvi, PhD
- Email: slrizvi@rutgers.edu
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- age 18 or older
- identifying as Chinese or Chinese American
- interested in learning coping skills to regulate emotions
- having a smart-phone compatible with the research mobile phone app
- matriculated at the local University for the current semester
Exclusion Criteria:
- currently receiving routine mental health services
- not able to read or write English
- not able to provide informed consent
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 |
---|---|
No Intervention: Assessment only
Daily assessment of emotion regulation and self-efficacy variables.
|
|
Experimental: Acceptance-oriented skills followed by change-oriented skills
Administration of acceptance-oriented skills videos first followed by change-oriented skills videos.
|
A series of 14 animated videos (9 acceptance-oriented and 5 change-oriented skills videos) available in both English and Mandarin Chinese.
|
Experimental: Change-oriented skills followed by acceptance-oriented skills
Administration of change-oriented skills videos first followed by acceptance-oriented skills videos.
|
A series of 14 animated videos (9 acceptance-oriented and 5 change-oriented skills videos) available in both English and Mandarin Chinese.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Emotion regulation measured by a combination of questions
Time Frame: daily for up to 4 weeks
|
A combination of questions on emotional states, context for emotions, how intolerable and distressing emotions are, use of emotion regulation strategies, perceived effectiveness of emotion regulation, and Patient-Reported Outcomes Measurement Information System Self-efficacy of Managing Emotions Short-form 4a (a 4-item measure of the confidence to manage emotional states rated using a 5-point Likert scale)
|
daily for up to 4 weeks
|
General self efficacy measured by Patient-Reported Outcomes Measurement Information System General Self-Efficacy Short-form 4a
Time Frame: daily for up to 4 weeks
|
A 4-item measure of the ability to successfully perform specific tasks and behaviors rated using a 5-point Likert scale
|
daily for up to 4 weeks
|
Acceptability/usability of intervention measured by a combination of Likert-scale and open-ended questions
Time Frame: daily following the delivery of each video for up to 2 weeks
|
A combination of questions that involve rating the acceptability and usability of skills videos (e.g., "how useful do you think the skills will be") and open-ended questions on cultural relevance
|
daily following the delivery of each video for up to 2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Qingqing Yin, M.S., Rutgers, the State University of New Jersey
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)
September 18, 2023
Primary Completion (Estimated)
June 1, 2024
Study Completion (Estimated)
August 1, 2024
Study Registration Dates
First Submitted
August 8, 2023
First Submitted That Met QC Criteria
September 3, 2023
First Posted (Actual)
September 5, 2023
Study Record Updates
Last Update Posted (Actual)
March 22, 2024
Last Update Submitted That Met QC Criteria
March 20, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Pro2023001220
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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