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Parent-Child Single-Session Growth Mindset Intervention on Adolescent Depression and Anxiety Problems

Effects of Parent-Child Single-Session Growth Mindset Intervention on Adolescent Depression and Anxiety Problems: A Three-Arm Waitlist Randomised Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05493865
Enrollment
549
Registered
2022-08-09
Start date
2024-09-01
Completion date
2025-10-31
Last updated
2024-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, Anxiety

Keywords

implicit theory, fixed mindset, mental health, secondary school students, belief in change

Brief summary

Depression and anxiety are common mental health problems among adolescents worldwide. In Hong Kong, one in every four secondary school students reports clinical-level depression or anxiety symptoms. Extant research has found that a fixed mindset on intelligence and emotions and failure-is-debilitating belief are closely related to more depression and anxiety symptoms, hopelessness, and suicidality. At the same time, recent research also points to the importance of parental mindset. Parents are the primary social support of adolescents; parental belief systems can strongly influence children's affect, behaviour, and mental health. However, the effects of parent-child mindset interventions on a child's internalising problems have not yet been empirically examined. As emerging evidence has shown the promise of single-session interventions in reducing and preventing youth internalising problems, this project develops and examines a parent and child single-session intervention on mindsets of intelligence, failure, and emotion (PC-SMILE) - to tackle depression and anxiety in young people and promote parental well-being. Using a three-arm randomised controlled trial, the proposed study will examine the effectiveness of PC-SMILE on reducing depression and anxiety symptoms among children, enhancing well-being and parent-child relationships. A total of 549 parent-child dyads will be recruited from six secondary schools and randomly assigned to either the PC-SMILE intervention group, the C-SMILE intervention group, or the no-intervention waitlist control group. The intervention is approximately 45 minutes in length. In the PC-SMILE group, both parent and child will receive intervention, and their mental health and family relationship will be assessed at three time points: baseline before intervention (T1), within two weeks post-intervention (T2), and three months post-intervention (T3). In the C-SMILE group, only the child will undergo intervention, while both the child and parent will be required to complete the repeated assessments. A pilot test (n = 9) has supported the feasibility and acceptability of the PC-SMILE intervention. We hypothesise that compared to the waitlist control group, the PC-SMILE intervention group and C-SMILE group will significantly improve child depression and anxiety (primary outcome) and significantly improve secondary outcomes, including children's academic self-efficacy, hopelessness, psychological well-being, and parent-child interactions and relationships, and PC-SMILE group is more effective than C-SMILE group. The intention-to-treat principle and linear-regression-based maximum likelihood multi-level models will be used for data analysis. As of May 2024, we enrolled 75 students and their parents in the study. This study will not only provide evidence on parent-child growth mindset intervention for adolescent internalising problems but can also serve as a scalable and accessible intervention for improving the well-being of young people and their parents.

Interventions

BEHAVIORALThe Parent-Child Single-Session-intervention of Mindset Intelligence, Failure and Emotion (PC-SMILE)

This study will be a three-arm cluster-randomised controlled trial to examine the efficacy of the PC-SMILE for adolescents by comparing to a C-SMILE intervention group and a no-intervention waitlist control group.

Sponsors

The Hong Kong Polytechnic University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

Due to the nature of intervention, blinding participants to the allocation is impossible. But Before the intervention starts, participants have no knowledge on which group they are belonging to.

Eligibility

Sex/Gender
ALL
Age
11 Years to 16 Years
Healthy volunteers
Yes

Inclusion criteria

* The inclusion criteria for adolescent participants are: 1. aged between 11-16 (inclusive) with one parent willing to participate; 2. Chinese youth who can read and write in Chinese; 3. sufficient visual and auditory abilities to complete the intervention and assessment; 4. ability to give consent to participate in the study. * The inclusion criteria for parent participants are: 1. living with the child participant; 2. Chinese-language proficiency and comfort with completing computer-based activities; 3. sufficient visual and auditory abilities to complete the intervention and assessment; 4. ownership of personal internet-equipped devices.

Exclusion criteria

*

Design outcomes

Primary

MeasureTime frameDescription
Children's depression and anxiety symptomsbaseline25-item Revised Children's Anxiety and Depression Scale (RCADS-25)

Secondary

MeasureTime frameDescription
Parent-child interactionsbaselinethree questions about how many days the children spend more than 15 minutes per day doing activities with their parents in a week
Children's hopelessnessbaselinethe four-item Hopelessness Scale
Children's psychological well-beingbaselinethe Warwick-Edinburgh Mental Well-Being Scale-7
Children's academic self-efficacybaselinea 5-item scale that was adapted from the part of Patterns of Adaptive Learning Survey
Parent-child relationshipsbaselinethree items
Perceived parent learning versus performance orientationbaseline8 items for children and 12 items for parents to indicate the extent to which reactions parents would have and which reactions children would perceive
Parents' psychological well-beingbaselinethe Warwick-Edinburgh Mental Well-Being Scale-7

Contacts

Primary ContactShimin Zhu, phD
jasmine.zhu@polyu.edu.hk+85251187809

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 19, 2026