- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05056428
Effects of Mindfulness Training on Emotional Care Strategies
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
All the participants will complete an online survey before (baseline), after (post-intervention), and two-months (follow-up) after the intervention. A subset of participants (N = 30) will complete an electroencephalography (EEG) experiment.
Prior to the experiment, participants will complete an online questionnaire writing down eight recent autobiographical situations: four reflecting a neutral experience, two reflecting events that triggered anxiety, and two reflecting events that triggered sadness. After writing about each situation, participants will be asked to identify five keywords that are both unique and tightly linked to each situation.
During the experiment, participants will be reminded of the autobiographical situations in the computerized task. Participants will be asked to view the keywords (i.e. control condition); step back and view the keywords like an impartial observer, allowing whatever thoughts or emotions arise to come and go (i.e. decentering condition); and think about the keywords from different perspective to minimize negative emotions (i.e. reappraisal condition). EEG will be recorded while participants complete the task. Participants will receive $200 Hong Kong dollars each time as a remuneration for the time to participate in the experiment.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Hong Kong, Hong Kong
- Jockey Club "Peace and Awareness" Mindfulness Culture in Schools Initiative, Faculty of Social Sciences, The University of Hong Kong
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Aged 18 years old or above
- Working in local schools or education institutions
- Willing to participate in mindfulness training voluntarily
Exclusion Criteria:
- Have history of neurological or psychiatric disorder, brain injury, birth complications, or significant sensory impairment
- Currently under medications that are known to affect the brain (e.g. anti-depressants, epileptica, tranquilizer, sleep medication, psychotropics, ritalin, concerta, etc.)
- Experiencing severe or unstable mental health condition currently
- Completed 8-week mindfulness training previously
- Unwilling to go by random assignment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention group
8-week mindfulness program
|
The .b
Foundations course is an 8-week mindfulness program developed by Mindfulness in Schools Project (MiSP) for school teachers and personnel.
It includes a taster session and 8 weekly sessions.
Each session lasts for 1.5 hours with a specific theme (e.g.
Lesson 1 waking up from autopilot).
Formal and informal mindfulness practices (e.g.
mindful eating, body scan, mindful walking, habit releaser etc.), psychoeducation, cognitive exercises, inquiry, and home practice are involved.
|
|
No Intervention: Wait-list control
Participants in wait-list control group will receive the same intervention, two months after experimental group completed the intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in General Health
Time Frame: Baseline, Immediately after intervention, Two-months after intervention
|
General Health Questionnaire (GHQ), 12 items, 5-point Likert scale ranging from 1 (never) to 5 (always)
|
Baseline, Immediately after intervention, Two-months after intervention
|
|
Change in Stress
Time Frame: Baseline, Immediately after intervention, Two-months after intervention
|
Perceived Stress Scale (PSS), 10 items, 5-point Likert scale ranging from 1 (never) to 5 (always)
|
Baseline, Immediately after intervention, Two-months after intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Positive affect
Time Frame: Baseline, Immediately after intervention, Two-months after intervention
|
Positive and Negative Affect Schedule (PANAS), 4 items, 5-point Likert scale ranging from 1 (never) to 5 (always)
|
Baseline, Immediately after intervention, Two-months after intervention
|
|
Change in Negative affect
Time Frame: Baseline, Immediately after intervention, Two-months after intervention
|
Positive and Negative Affect Schedule (PANAS), 4 items, 5-point Likert scale ranging from 1 (never) to 5 (always)
|
Baseline, Immediately after intervention, Two-months after intervention
|
|
Change in Mindfulness
Time Frame: Baseline, Immediately after intervention, Two-months after intervention
|
Cognitive and Affective Mindfulness Scale-Revised (CAMS-R), 12 items, 5-point Likert scale ranging from 1 (never) to 5 (always)
|
Baseline, Immediately after intervention, Two-months after intervention
|
|
Change in Decentering
Time Frame: Baseline, Immediately after intervention, Two-months after intervention
|
Non Reactivity Subscale of Chinese Five Facet Mindfulness Questionnaire (FFMQ-C), 4 items, 5-point Likert scale ranging from 1 (never) to 5 (always)
|
Baseline, Immediately after intervention, Two-months after intervention
|
|
Change in Reappraisal
Time Frame: Baseline, Immediately after intervention, Two-months after intervention
|
Reappraisal subscale of Emotion Regulation Questionnaire (ERQ), 6 items, 5-point Likert scale ranging from 1 (never) to 5 (always)
|
Baseline, Immediately after intervention, Two-months after intervention
|
|
Change in Late positive potential (LPP)
Time Frame: Baseline, Immediately after intervention
|
A measure of emotional reactivity in EEG experiment; the amplitude of event-related potential (ERP) time-locked to the presentation of emotional stimulus (-200ms to 6000ms).
|
Baseline, Immediately after intervention
|
Collaborators and Investigators
Sponsor
Collaborators
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
Keywords
Other Study ID Numbers
- UHongKong (JC PandA)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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