Visual arts intervention for stroke survivors

A Theory-driven Visual Arts-based Intervention on Psychosocial Outcomes Among Community-dwelling Chinese Stroke Survivors

NA · The Nethersole School of Nursing · NCT05806658

This study is testing whether a four-week art program can help stroke survivors feel better and improve their social well-being compared to regular care.

Quick facts

PhaseNA
Study typeInterventional
Enrollment148 (estimated)
SexAll
SponsorThe Nethersole School of Nursing (other)
Locations1 site (Macau)
Trial IDNCT05806658 on ClinicalTrials.gov

What this trial studies

This study evaluates a theory-driven visual arts-based intervention aimed at improving psychosocial outcomes for community-dwelling stroke survivors. It involves a two-arm randomized controlled trial where participants are assigned to either a four-week visual arts intervention group or a usual stroke care control group. The intervention is grounded in Bandura's Self-Efficacy Theory, focusing on enhancing self-efficacy and psychosocial functioning. The study aims to assess the effectiveness and feasibility of this approach in a community setting.

Who should consider this trial

Good fit: Ideal candidates for this study are community-dwelling stroke survivors aged 18 and above, who are at least three months post-stroke and have a certain level of cognitive and physical function.

Not a fit: Patients with other pre-existing disabilities, severe communication impairments, or those currently engaged in other psychosocial recovery research may not benefit from this study.

Why it matters

Potential benefit: If successful, this intervention could significantly enhance the psychosocial well-being and self-efficacy of stroke survivors living in the community.

How similar studies have performed: Previous studies have indicated benefits of visual arts-based interventions for stroke recovery, but this approach is novel in its theoretical framework application.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Aged 18 years old or above
2. A clinical diagnosis of first-ever or recurrent ischaemic or haemorrhagic stroke
3. At least three months after stroke onset
4. Living at home
5. Hong Kong Montreal Cognitive Assessment (HK-MoCA) above the second percentile
6. At least stage four of upper limb function was assessed by Brunnstrom recovery stages (BRS)
7. Able to remain in a sitting position on a chair or wheelchair independently or with support
8. Able to communicate with Cantonese or Putonghua
9. Able to read traditional or simplified Chinese
10. Able to provide written informed consent

Exclusion Criteria:

1. Other diagnoses or diseases causing pre-existing physical disability or psychosocial problems
2. Dysphasia, hearing, or visual impairments
3. Any substance abuse affected their health status
4. Already taken a visual arts-based intervention for stroke recovery
5. Currently taking part in other research for psychosocial recovery
6. Currently receiving psychosocial therapy or intervention

Where this trial is running

Macau

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.

View on ClinicalTrials.gov →

Conditions: Stroke, Psychosocial Problem, Psychosocial functioning, Self-Efficacy

Last reviewed 2026-05-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.