- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06440785
Taylor Swift and Mental Health Outcomes
The Relation Between Following Taylor Swift on Social Media, Connecting With Her Music and Mental Health Outcomes in Youths: Cross-sectional Survey Study
Study Overview
Status
Conditions
Detailed Description
Background: Epidemiological surveys suggest that young adulthood is the age group with the highest prevalence of mental illness. However, many young adults have negative views towards help-seeking and do not access professional services. To address this gap, popular culture may provide population-level levers to improve mental health outcomes.
Objective: In this study, we will focus on Taylor Swift - a singer whose songs explore themes related to mental health. As the first objective, we will seek to understand whether young adults will feel a personal connection to her mental health-themed songs and follow her on social media. We will then examine whether these forms of engagement will predict attitudes critical for help-seeking: namely, acknowledgement that one may have a mental illness, and willingness to seek professional services as needed.
Methods: In the months leading up to Taylor Swift's concerts, we will conduct a survey of over 600 young adults in Singapore (aged 18 to 34). As the primary outcome measures, participants will complete the Self-Identification as Having Mental Illness Scale (SELFI) and the Inventory of Attitudes toward Seeking Mental Health Services scale (IASMHS). As predictor variables, participants will answer questions related to: (i) their baseline symptoms of depression, anxiety, and stress; (ii) their engagement with Taylor Swift's songs and social media content; and (iii) their demographics.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Sundarimaa Erdembileg
- Phone Number: +65 6601-1000
- Email: sundarimaa.e@u.yale-nus.edu.sg
Study Locations
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Singapore, Singapore
- Recruiting
- Yale-NUS
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Contact:
- Jean Liu, PhD
- Phone Number: +65 6601-3694
- Email: jeanliu@yale-nus.edu.sg
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Enrollment is restricted to healthy adults between 18-34
- Use at least one of the following social media platforms: Facebook, Instagram, LinkedIn, X (Twitter), TikTok
- Have lived in Singapore for at least 2 years.
- Participants need to be able to read and understand English.
Exclusion Criteria:
- Anyone who does not feel comfortable answering questions related to mental health and exposure to mental health-related content online.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Help-Seeking Behaviors
Time Frame: Through study completion, an average of 1 year
|
Inventory of Attitudes toward Seeking Mental Health Services (IASMHS).
Items were on a 5-point Likert scale ranging from 0 ("Somewhat Disagree") to 4 ("Agree").
|
Through study completion, an average of 1 year
|
|
Self-Diagnosing Behaviors for Mental Health
Time Frame: Through study completion, an average of 1 year
|
Self-identification as having a Mental Illness (SELF-I) scale.
Items were on 5-point Likert scale ranging from 1 (Not true at all) to 5 (Completely True)
|
Through study completion, an average of 1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sundarimaa Erdembileg, Yale-NUS College
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NUS-IRB-2023-864B
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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