Depression Mental and Behavioural Disorders
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Hong Kong junior secondary students, aged 11-15 from band 1 – 2 were recruited for the study. 2. S.2-3 students, aged between 11-15; 3. Ability to understand and communicate in Cantonese; 4. Medical conditions that are likely to limit group participation during the course of the 6-week program will be excluded; and 5. Willing to perform art making activities in group activities with minimal assistance.
Exclusion criteria
Exclusion criteria: Participants were excluded if they had been clinically diagnosed with depressive disorder, anxiety disorder, or any other psychiatric disorder that required medical treatment or professional intervention during the past 12 months, diagnosed with other medical conditions or receiving counselling treatment during the program. Both parents and the participants gave written informed consent prior to the screening procedures and joining the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measured at T0 (baseline), T1 (after completion of the intervention), and T2 (8 weeks following the completion of the intervention): 1. Salivary cortisol measured using the “Salivette” kits (Starstedt, Ag & Co., Numbrecht, Germany) 2. Emotion regulation measured using the State Difficulties in Emotion Regulation Scale (S-DERS) 3. Emotion measured using the Positive and Negative Affect Schedule (PANAS) 4. The 25-item Connor-Davidson Resilience Scale (CD-RISC) 5. Emotional awareness measured using the Toronto Alexithymia Scale (TAS-20) | — |
Secondary
| Measure | Time frame |
|---|---|
| Experiences of the intervention measured using focus groups at completion of the intervention | — |
Countries
China, Hong Kong