- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06732297
Stronger Families Through Art Therapy: A Mixed Methods Programme Evaluation Study (SFAT)
The current research aims to evaluate the effectiveness and feasibility of the Strong Families 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:
- Is the programme effective in enhancing quality of life and family resilience among parents?
- Is the programme effective in enhancing quality of life among children?
- Is the programme feasible and acceptable for large scale implementation in Singapore?
Researchers will compare the status of family participants (caregivers and children) before and after they take the programme and compare family participants who take the programme with family participants who have not yet taken the programme to see if the programme is effective in benefiting the participants. Researchers will also invite family participants to discuss about the programme.
Family participants will
- Take the 10-week SFAT programme
- Complete assessment survey for 3 times
- Attend a focus group discussion (optional)
To assess the programme feasibility, researchers will additional invite art therapist participants to evaluate the programme and invite community staff participants to discuss about the programme implementation.
Art therapist participants will complete programme and session evaluation reports.
Community staff participants will attend a focus group discussion.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Andy Hau Yan Ho, PhD, EdD
- Phone Number: +65 6316 8943
- Email: andyhyho@ntu.edu.sg
Study Contact Backup
- Name: Stephanie Hilary Xinyi Ma, PhD
- Email: stephaniehilary.ma@ntu.edu.sg
Study Locations
-
-
-
Singapore, Singapore, 150082
- Recruiting
- The Red Pencil Singapore
-
Contact:
- Vivyan Yeo
- Phone Number: +65-62212217
- Email: programme@redpencil.org
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria (family participant):
- the caregiver (including parents, grandparents, family members or foster parents who perform the main caretaking responsibilities of the children taking part in SFAT) of a young child who can communicate in English and provide informed consent
- the child is aged 7-14 years and can communicate in English
- the family have one or more of the following identified challenges: (1) caregiver stress such as finances, household management, work and childcare arrangements, (2) caregiver struggles to find time for self-care and quality time with children, (3) caregiver has minimal understanding of the psychological and emotional needs of their children, (4) children face difficulties with emotional regulation and anger management
- caregivers and children are from low-income families who receive financial assistance under the CHAS Blue card, ComCare financial assistance, and/or the MOE Financial Assistance Scheme
Inclusion criteria (art therapist participant) registered art therapist based in the Red Pencil (Singapore) who are in charge of delivering the SFAT programme
Inclusion criteria (community staff participant)
- community staff who provides assistance to the implementation of the SFAT programme
Exclusion Criteria:
- individuals who are suffering from depression or other major mental health conditions that would render their participation highly disruptive to others in a group setting, and/or cannot provide informed consent. Families will also be excluded if they are currently unstable (i.e. circumstances related to abuse/neglect), and/or have high risk of suicidal and self-harm behaviours. In the cases that individuals referred to the programme are not eligible, the partner organisations will assess their needs and refer them to programmes based on these needs.
- participant is unable to provide informed consent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Immediate Treatment Group
Family participants in the immediate treatment group will undergo the intervention after baseline assessment and randomization.
The intervention consists of 1.5-hour art-therapy sessions which happen every week for 10 weeks.
The topics of intervention sessions include building rapport, emotional expression & regulation, self-care, communication & collaboration, and reflection & community.
|
The Stronger Families Through Art Therapy (SFAT) is a dyadic art therapy intervention 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.
|
|
Other: Waitlist Control Group
Family participants in the waitlist control group will undergo the intervention after participants in the immediate treatment group complete the intervention.
Participants in the two group undergo the same intervention.
|
The Stronger Families Through Art Therapy (SFAT) is a dyadic art therapy intervention 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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-rated quality of life for caregiver participants
Time Frame: From enrollment to the end of assessment at 20 weeks
|
The primary outcome will be assessed by the World Health Organization Quality of life Brief Scale (WHOQOL-BREF) [WHO, 1997].
The WHOQOL-BREF comprises 26-items rated on a 5-point Likert scale and clustered into the four subscales of physical health, psychological health, social relationships, and environmental health.
The WHOQOL-BREF possesses strong internal validity, reliability, and cross-cultural applicability.
|
From enrollment to the end of assessment at 20 weeks
|
|
Self-rated quality of life for child participants
Time Frame: From enrollment to the end of assessment at 20 weeks
|
The primary outcome will be assessed by the KIDSCREEN-30 tool [Ravens-Sieberer, U., et al., 2013].
The KIDSCREEN-30 comprises of 30 items rated on a 4-point visual Likert scale and clustered into the 8 domains of physical wellbeing, psychological wellbeing, moods and emotions, autonomy and parent relation, financial resources, social support and peers, school environment and social acceptance.
KIDSCREEN30 possesses strong internal validity, reliability, and cross-cultural applicability.
|
From enrollment to the end of assessment at 20 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-rated family resilience for caregiver participants
Time Frame: From enrollment to the end of assessment at 20 weeks
|
The secondary outcome will be assessed by the Walsh Family Resilience Questionnaire (WFRQ) [Walsh, 2016].
The WFRQ comprises 32 items rated on a 5- point Likert Scale and clustered into the 3 subscales of belief systems, organisational pattens, and communication/problem solving.
The WFRQ possesses strong internal validity, reliability, and cross-cultural applicability
|
From enrollment to the end of assessment at 20 weeks
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- IRB-2024-821
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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