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The current research aims to evaluate the effectiveness and feasibility of the Strong Family Through Art Therapy (SFAT) programme, which was developed to improve the parent-child relationship in vulnerable families. The main questions it aims to answer are:
Researchers will compare participants before and after they take the programme and compare participants who take the programme with participants with participants who have not yet taken the programme to see if the programme is effective in benefiting participants. Researchers will also invite participants to discuss together and interview art therapists to see if the programme is feasible and acceptable.
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The current research aims to evaluate the effectiveness and feasibility of the Strong Family Through Art Therapy (SFAT) programme, which was developed to improve the parent-child relationship in vulnerable families. Service users of the SFAT programme will receive a progressive support from workshops, dyad art therapy, and an innovative art-based self-care tool developed with a multidisciplinary team to meet the needs of enhancing family communication and strengthening emotional bonding. The current research utilizes a pragmatic mixed method research paradigm to evaluate the programme. For the quantitative component, a single-site, open label, Waitlist Randomized Control Trial (RCT) design, comprising two arms: (i) treatment group and (ii) waitlist control group, will be adopted to evaluate the efficacy of the Strong Family Through Art Therapy (SFAT) for improving quality of life and family resilience among parents and children. For the qualitative component, an embedded qualitative focus group evaluation study with participants who complete the SFAT programme, together with analysis of intervention session evaluation forms completed by the RPS art therapists who conduct the SFAT programme, will be conducted to evaluate programme acceptability and feasibility. After signing the informed consent form, the recruited family(consisting of one parent and one to three children dyads) will be asked to complete a baseline assessment before randomization and the start of the SFAT programme [T1]. Treatment group participants will then undergo an 10-week SFAT programme conducted by the RPS clinical team, complete an immediate post-intervention assessment [T2], with a final follow-up assessment at 20-weeks [T3]. The waitlist control group will complete a pre-intervention assessment before start of the SFAT programme at 10-weeks [T2], then undergo the same 10-week SFAT programme conducted by the RPS clinical team and complete an immediate post-intervention assessment at 20-weeks [T3]. Moreover, selected participants will be invited to take part in an acceptability focus group study after T3 assessments. Post-session evaluation forms will also be completed by RPS art therapists after session completion. Figure 1 details the study procedures.
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96 participants in 2 patient groups
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Andy Hau Yan Ho, PhD, EdD; Stephanie Hilary Xinyi Ma, PhD
Data sourced from clinicaltrials.gov
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