- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06090760
Mindfulness Intervention and Online Social Networking
April 22, 2024 updated by: GU Mingyue Michelle, Education University of Hong Kong
Mindfulness Intervention on Wellbeing During OSN
This study aims to examine (a) the effects of mindfulness-based intervention on wellbeing including psychological, social, and emotional wellbeing, depressive symptoms, and stress and (b) the extent to which demographics, OSN use, and mindfulness mediate these effects.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
76
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: Ngar-sze Lau, PhD
- Phone Number: +852 39436913
- Email: ngarszelau@cuhk.edu.hk
Study Contact Backup
- Name: Jincheng Ding, MA
- Phone Number: +852 29486428
- Email: djincheng@eduhk.hk
Study Locations
-
-
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Hong Kong, Hong Kong
- Ngar-sze Lau
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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:
- Over 18 years old
Exclusion Criteria:
- have not complete the application form
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Mindfulness Intervention Group
Mindfulness training will be provided to the participant after randomization for dealing with social media use.
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Mindfulness is "paying attention in a particular way: on purpose, in the present moment, and non-judgmentally" (Kabat-Zinn 1994, 4) and has five facets: awareness, nonjudgement, nonreactive, observe, and describe (Baer et al., 2006).
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No Intervention: Waitlist Control Group
No mindfulness training will be provided to the participants.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Social Media Engagement
Time Frame: 8 weeks
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The Social Media Engagement Scale
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8 weeks
|
Well-being
Time Frame: 8 weeks
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Well-being Scale
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8 weeks
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Emotion
Time Frame: 8 weeks
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Difficulties in Emotion Regulation Scale
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8 weeks
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Depression
Time Frame: 8 weeks
|
Depression and Anxiety Stress Scales
|
8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Michelle Gu, PhD, The Education University of Hong Kong
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 27, 2023
Primary Completion (Actual)
March 29, 2024
Study Completion (Estimated)
May 19, 2024
Study Registration Dates
First Submitted
October 13, 2023
First Submitted That Met QC Criteria
October 13, 2023
First Posted (Actual)
October 19, 2023
Study Record Updates
Last Update Posted (Actual)
April 24, 2024
Last Update Submitted That Met QC Criteria
April 22, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- EduUHK01
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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