Jockey Club Support Project
Condition(s) studied
Investigational drug(s) / intervention(s)
Emotion Regulation Skills Training: This arm will receive training in emotion regulation skills, including mindfulness skills to help redeploy their attention, cognitive reappraisal skills to analyze stimuli or emotion-eliciting events from a more comprehensive perspective, situation change skills to regulate emotions by exposing oneself to nature, experiential acceptance skills through metaphor, and breathing techniques. They will also receive training in theories of the family emotion system.
Moderation in Consumer Electronics Use Training: This arm will be trained to moderate their and their family members' use of commercial electronics. They will do so by learning mechanisms behind addictions, family communication skills, and various substitute activities for commercial electronics usage.
Study summary
Guided by the process model of emotion regulation, integrative affect-regulation framework for resilience, and the reciprocal dynamics of emotion, affect, and resilience in the family system, researchers will develop a parallel intervention to incorporate two key members in Mainland-Hong Kong cross-boundary families: a parent and a child by improving their affect/emotion regulation skills, de-escalate family conflicts, and flourish under hardships. Specifically, researchers predict that participants in the intervention group will report greater improvement in resilience, emotion regulation, psychological well-being, family harmony, and social connectedness than those in the control group.
Eligibility
Primary outcome measure(s)
- Resilience — Baseline, 4 weeks, 8 weeks
Participants' psychological resilience will be measured by the 25-item Connor-Davidson Resilience Scale. Participants will report their perceived psychological resilience of self on a 5-point Likert scale (0 = strongly disagree; 4 = strongly agree). Higher total scores indicate higher levels of psychological resilience. - Cognitive Emotion Regulation — Baseline, 4 weeks, 8 weeks
Participants' use of adaptive cognitive emotion regulation strategies will be measured by corresponding subscales of the Cognitive Emotion Regulation Questionnaire (CERQ). The study will employ five subscales, including acceptance, positive refocusing, refocus on planning, positive reappraisal, and putting into perspective, as these strategies are the targets of the intervention. Each subscale includes four items. Participants will report their use of each strategy on a 5-point Likert scale (1 = almost never; 5 = almost always). Higher scores for each subscale indicate more use of the corresponding cognitive emotion regulation strategy. - Behavioral Emotion Regulation — Baseline, 4 weeks, 8 weeks
Participants' use of adaptive behavioral emotion regulation strategies will be measured by corresponding subscales of the Behavioral Emotion Regulation Questionnaire (BERQ). The study will employ two subscales (seeking distraction and putting into perspective) as these strategies are the targets of the intervention. Each subscale includes four items. Participants will report their use of each strategy on a 5-point Likert scale (1 = almost never; 5 = almost always). Higher scores for each subscale indicate more use of the corresponding behavioral emotion regulation strategy. - Affective Experiences — Baseline, 4 weeks, 8 weeks
Participants' affective experiences will be measured by the International Positive and Negative Affect Schedule Short Form (I-PANAS-SF). Participants will report their experienced positive and negative affect on a 10-item, 5-point Likert scale (1 = never; 5 = always). Higher scores indicate higher levels of positive or negative affect. - Depression and Anxiety Symptoms — Baseline, 4 weeks, 8 weeks
Participants' depression and anxiety symptoms will be measured by the Patient Health Questionnaire (PHQ-4). On this 4-point Likert scale from 0 to 3, participants will report their frequency of depression and anxiety symptoms. Higher scores indicate more severe symptoms. - Well-being — Baseline, 4 weeks, 8 weeks
Participants will also complete the 5-item WHO Well-Being Index (WHO-5). They will report their well-being with a 6-point Likert scale (0 = at no time; 5 = all of the time). Higher scores indicate higher levels of well-being.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| International Social Service Hong Kong Branch | Shenzhen | Guangdong | Recruiting |
More City University of Hong Kong trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07136064 on ClinicalTrials.gov ↗ ← All trials in China