Patient Engagement Clinical Trial
— ARTS-REHABOfficial title:
The Royal Conservatory's ARTS-REHAB Project Research Study
The ARTS-REHAB Project Research Study examines how meaningful engagement in a creative process might impact inpatients in rehabilitation centres. Participants in this random control trial study will be recruited from a slow-stream rehabilitation patient population. The study intervention will consist of The Royal Conservatory's Living Through the Arts program. Data will be collected using structured and semi-structured questionnaires along with observational logs and focus groups. This study will explore the effects of the program, comparing the intervention and control group participants' sense of hope and optimism for returning to their daily lives, as well as their sense of engagement in their physical recovery.
Status | Recruiting |
Enrollment | 188 |
Est. completion date | April 2017 |
Est. primary completion date | April 2017 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 90 Years |
Eligibility |
Inclusion Criteria: 1. Eligible participants must be health care centre inpatients with an average expected length of stay of 30 days or longer; 2. Eligible participants need to be able to speak, understand, and write English; eligible participants also need to be cognitively able to understand and give written consent and complete research questionnaires (either independently or with minimal assistance); 3. Eligible participants are willing and able to take part in either the intervention group (Living Through the Arts programming) or in the control group; 4. Eligible participants were either community-dwelling or have had a short stay in acute care (no longer than 4 weeks) prior to admission; 5. Eligible participants who are anticipated to return to their homes/communities (or to continue with their rehabilitation as outpatients) following their reconditioning rehabilitation. Exclusion Criteria: - early patient discharge (prior to the completion of minimum number of 4 sessions); - inability of patient to complete questionnaires (due to physical pain or cognitive decline); - transfer of patient to acute care (without return to slow-stream rehabilitation); and - (anticipated) transfer of patient to long-term care following rehabilitation. |
Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care
Country | Name | City | State |
---|---|---|---|
Canada | The Royal Conservatoy of Music | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
The Royal Conservatory of Music | Ontario Trillium Foundation |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Hope and optimism measured through pre- and post- program questionnaires | Primary outcome will be measured through pre- and post- program questionnaires administered upon patient intake and prior to patient discharge. | 30 - 90 days | No |
Primary | Future purpose measured through pre- and post- program questionnaires | Primary outcome will be measured through pre- and post- program questionnaires administered upon patient intake and prior to patient discharge | 30 - 90 days | No |
Primary | patient engagement measured through pre- and post- program questionnaires | Primary outcome will be measured through pre- and post- program questionnaires administered upon patient intake and prior to patient discharge | 30-90 days | No |
Secondary | Length of stay | Difference scores will be calculated using patient admission and discharge dates (both anticipated and actual discharge dates). | 30-90 days | No |
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