- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03729648
Expressive Arts-based Intervention for Young and Pre-elderly Stroke Survivors
The Psycho-physiological & Social-spiritual Effects of Expressive Arts-based Intervention on Young and Pre-elderly Stroke Survivors: A Randomized Controlled Study
Study Overview
Detailed Description
Stroke is a devastating illness that induces numerous impairments of body function and structure, and limitations to activities in all aspects of life, thus imposing multi-faceted restrictions on one's participation in daily living. It also has detrimental impacts on one's mental health, social relationship, and quality of life. Stroke survivors often face challenges arising from the illness and its disabilities, as well as the resulting deterioration of occupational functioning. They also suffer from the psycho-spiritual sequels of loss in functioning, sense of worthlessness and hopelessness, and fear of relapse, all of which could result in mental health distress such as depression, anxiety, stress, isolation, and impaired quality of life. Though the risk of stroke increases with age, statistics have documented an increasing trend of a younger age of onset. The issues faced by younger and pre-elderly stroke survivors (<65 years old) will be even more severe due to longer term of survival, problems of resuming their occupations, and lacking of social welfare and resources for their pre-elderly age.
Existing research focuses primarily on older adults stroke survivors; this study is set out to contribute to current knowledge of the effectiveness of arts-based rehabilitation on younger stroke survivors. Both psychological and physiological outcomes will be examined for a comprehensive understanding on the biological, psychological, social, and spiritual changes after participating in a non-pharmacological, engaging, safe and enjoyable multi-modal expressive arts-based intervention approach of rehabilitation.
Examination on the relationships among bio-psycho-social-spiritual variables may help understand the complex relationships among these factors after stroke and during rehabilitation, which will contribute to the development of holistic care for stroke survivors.
This current study will adopt a 2-arm randomized controlled design with treatment-as-usual control. Upon screening for inclusion exclusion criteria, baseline data will be collected; and eligible participants will be randomized into either an 8-week Expressive Arts-based intervention group or Treatment-As-Usual control group. The control group will continue with routine rehabilitation service and have the option to participate in the Expressive Arts-based Intervention Group upon study completion. Participants will be assessed 3 times at baseline (T0), post-intervention (8th week, T1), and 6-month post-intervention (T2). The participants will complete the study in about 8 months.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Hong Kong, Hong Kong
- Centre on Behavioral Health HKU
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Presence of a single-lesion stroke in the left or right, temporal, frontal, parietal or subcortical brain region
- Experienced a major stroke event within 120 months from the time of study participation
- Diagnosis of either (a) ischemic or (b) hemorrhagic stroke
- Disability grade 1 to 4 on the Modified Rankin Scale
- With residual functions of the affected extremity
- The ability to understand instructions, both verbal and written in Chinese, and;
- Ages 18 to below 65
Exclusion Criteria:
- Concurrent diagnosis of major medical or psychiatric disorders other than stroke (except depression)
- Currently receiving hospital treatment and care
- Presence of hearing or visual deficits, even with aids
- Total paralysis of the upper limbs
- Amputation of one of the limbs
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: Intervention
This arm of participants will be receiving Expressive Arts Therapy as intervention
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The intervention brings together the strengths of different art modalities, such as visual art, music, movement, dance, drama and writing to assist reflect and response in individuals to their personal issues.
Such variety of art forms multiplies the avenues by which a person in therapy may seek meaning, clarity, insight and healing.
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No Intervention: Control
This arm of participants will not receive any intervention and are allocated as a wait-list control group
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change from Baseline Depression and Anxiety level at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8
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Administration of the Chinese translated version of Hospital Anxiety and Depression Scale
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Baseline, Month 2, and Month 8
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Change of Baseline Perceived Stress level at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8
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Administration of Chinese translated version of Perceived Stress Scale
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Baseline, Month 2, and Month 8
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Change of Baseline Perceived Social Support level at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8
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Administration of the Chinese version of the Multidimensional Scale of Perceived Social Support
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Baseline, Month 2, and Month 8
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Change of Baseline general quality of life at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8
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Administration of the Chinese version of the 12-item Short Form Health Survey
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Baseline, Month 2, and Month 8
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Change of Baseline Physical stress level and cortisol rhythm at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8
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Collection of saliva samples for analysis
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Baseline, Month 2, and Month 8
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Change of Baseline Self-esteem at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8
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Administration of the Chinese version of the Rosenberg Self-esteem Scale
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Baseline, Month 2, and Month 8
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Change of Baseline Hope level at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8
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Administration of the Chinese version of the Adult State Hope Scale
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Baseline, Month 2, and Month 8
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Change of Baseline Spiritual well-being level at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8
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Administration of the Chinese version of the 3-item spiritual care sub-scale of the Body-Mind-Spirit Holistic Well-being Scale
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Baseline, Month 2, and Month 8
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Change of Baseline Stroke-specific quality of life at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8
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Administration of the Chinese version of the Stroke-specific Quality of Life Short Form
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Baseline, Month 2, and Month 8
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Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 17609417
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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