Expressive Arts-based Intervention for Young and Pre-elderly Stroke Survivors

April 17, 2023 updated by: The University of Hong Kong

The Psycho-physiological & Social-spiritual Effects of Expressive Arts-based Intervention on Young and Pre-elderly Stroke Survivors: A Randomized Controlled Study

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. 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.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.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

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

Interventional

Enrollment (Actual)

154

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Hong Kong, Hong Kong
        • Centre on Behavioral Health HKU

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 64 years (Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. Presence of a single-lesion stroke in the left or right, temporal, frontal, parietal or subcortical brain region
  2. Experienced a major stroke event within 120 months from the time of study participation
  3. Diagnosis of either (a) ischemic or (b) hemorrhagic stroke
  4. Disability grade 1 to 4 on the Modified Rankin Scale
  5. With residual functions of the affected extremity
  6. The ability to understand instructions, both verbal and written in Chinese, and;
  7. Ages 18 to below 65

Exclusion Criteria:

  1. Concurrent diagnosis of major medical or psychiatric disorders other than stroke (except depression)
  2. Currently receiving hospital treatment and care
  3. Presence of hearing or visual deficits, even with aids
  4. Total paralysis of the upper limbs
  5. Amputation of one of the limbs

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
Experimental: Intervention
This arm of participants will be receiving Expressive Arts Therapy as intervention
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.
No Intervention: Control
This arm of participants will not receive any intervention and are allocated as a wait-list control group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from Baseline Depression and Anxiety level at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8

Administration of the Chinese translated version of Hospital Anxiety and Depression Scale

  • This scale is adopted to measure the level of Depression and Anxiety.
  • Two scores, Depression score and Anxiety score, are generated.
  • The minimum score is 0 and the maximum score is 21.
  • Scores ranging from "0-7" represents "Normal", ranging from "8-10" represents "Borderline abnormal", and ranging from "11-21" represents "Abnormal".
Baseline, Month 2, and Month 8
Change of Baseline Perceived Stress level at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8

Administration of Chinese translated version of Perceived Stress Scale

  • This scale is adopted to measure the level of perceived stress
  • The total score of Perceived Stress Scale is summing all the scores from each item, with Q4, Q5, Q7, and Q8 are reverse items.
  • The minimum score is 0 and the maximum score is 40.
  • Scores ranging from "0-13" represents low stress, ranging from "14-26" represents moderate stress, and "27-40" represents high perceived stress.
Baseline, Month 2, and Month 8
Change of Baseline Perceived Social Support level at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8

Administration of the Chinese version of the Multidimensional Scale of Perceived Social Support

  • This scale has adopted the measure the level of perceived social support from family, friends, or significant other.
  • The mean score of perceived social support from "family" is calculated by summing across Q3, Q4, Q8, and Q11, then divide by 4.
  • The mean score of perceived social support from "friends" is calculated by summing across Q6, Q7, Q9, and Q12, then divide by 4.
  • The mean score of perceived social support from "significant other" is calculated by summing across Q1, Q2, Q5, and Q10, then divide by 4.
  • The mean total score is calculated by summing across all 12 items, then divide by 12.
  • The minimum mean score of each sub-score and the total score is 1 and the maximum mean score is 7.
Baseline, Month 2, and Month 8
Change of Baseline general quality of life at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8

Administration of the Chinese version of the 12-item Short Form Health Survey

  • This scale is adopted to measure the level of health-related Quality of life.
  • Q1, Q8, Q9, and Q10 are reversed items.
  • Physical and Mental Health Composite Scale scores are calculated.
Baseline, Month 2, and Month 8
Change of Baseline Physical stress level and cortisol rhythm at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8
Collection of saliva samples for analysis
Baseline, Month 2, and Month 8
Change of Baseline Self-esteem at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8

Administration of the Chinese version of the Rosenberg Self-esteem Scale

  • This scale is adopted to measure the level of self-esteem.
  • Q2, Q5, Q6, Q8, Q9 are reversed items.
  • Total self-esteem score is calculated by summing all items.
  • The minimum score is 10 and the maximum score is 40.
  • A higher score represents a higher level of self-esteem.
Baseline, Month 2, and Month 8
Change of Baseline Hope level at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8

Administration of the Chinese version of the Adult State Hope Scale

  • This scale is adopted to measure the level of hope.
  • Pathways sub-scale score is calculated by summing across Q1, Q3, and Q5.
  • Agency sub-scale score is calculated by summing across Q2, Q4, and Q6.
  • Total hope score is calculated by summing all items.
  • The minimum score of the sub-scales is 3 and the maximum score of the sub-scales is 24.
  • The minimum score of the total score is 6 and the maximum score of the total score is 48.
  • The higher scores in sub-scales represent higher levels of pathways thinking or higher agency thinking respectively. The higher total score represents higher hope levels.
Baseline, Month 2, and Month 8
Change of Baseline Spiritual well-being level at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8

Administration of the Chinese version of the 3-item spiritual care sub-scale of the Body-Mind-Spirit Holistic Well-being Scale

  • This sub-scale is adopted to measure the level of spiritual well-being.
  • The sub-scale score is calculated by summing across all three items.
  • The minimum score of this sub-scale is 3 and the maximum score of this sub-scale is 30.
  • A higher score represents a higher level of spiritual well-being.
Baseline, Month 2, and Month 8
Change of Baseline Stroke-specific quality of life at 2 months and 8 months
Time Frame: Baseline, Month 2, and Month 8

Administration of the Chinese version of the Stroke-specific Quality of Life Short Form

  • This scale is adopted to measure the level of stroke-specific Quality of Life.
  • Physical components of stroke-specific Quality of Life is calculated by summing across Q1, Q2, Q4, Q7, Q10, Q11, and Q12.
  • Psychosocial components of stroke-specific Qualify of life is calculated by summing across Q3, Q5, Q6, Q8, and Q9.
  • The minimum score of physical and psychosocial components is 7 and 5 respectively.
  • The maximum score of physical and psychosocial components is 35 and 25 respectively.
  • A higher score represents a higher level of stroke-specific quality of life.
Baseline, Month 2, and Month 8

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2018

Primary Completion (Actual)

December 31, 2022

Study Completion (Actual)

December 31, 2022

Study Registration Dates

First Submitted

August 29, 2018

First Submitted That Met QC Criteria

October 31, 2018

First Posted (Actual)

November 5, 2018

Study Record Updates

Last Update Posted (Actual)

April 20, 2023

Last Update Submitted That Met QC Criteria

April 17, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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