Stroke Clinical Trial
— SHAPER-SOOfficial title:
Stroke Odysseys: Evaluation of a Community-based Performance Arts Programme for People That Have Experienced Stroke
| Verified date | August 2022 |
| Source | King's College London |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
There are over 1.2 million stroke survivors in the UK and annual costs of stroke care to the NHS will treble from £3.4 billion in 2015 to £10.2 billion in 2035. More than 60% of stroke survivors leave hospital with a disability, and half experience depression within the first five years. Emotional, social and psychological needs are common, often compounded by patients' perceptions of 'abandonment' when rehabilitation ends. Currently there is a gap between the social, emotional and physical needs of stroke survivors and the availability and suitability of long-term recovery and rehabilitation services. In 2018, a commissioned survey by the Stroke Association found 50% of stroke survivors and 85% of carers felt they needed more support than currently exists. Stroke Odysseys - the performance art programme- provides an opportunity for communication of experiences of stroke to an audience through acquired skills in movement, music, song and the spoken word. The performance arts courses delivered by Rosetta Life for stroke survivors have been evaluated in previous studies and have shown that engagement in and learning about performance skills can have a positive impact on perceptions of disability, improve cognition, mobility and speech disabilities among a stroke community that can be stigmatised by the public perception of disabling illness. The Stroke Odysseys programme will be scaled up to a large number of participants with the aim to evaluate the experience, impact and implementation of the programme. This prospective study will evaluate the experience and impact of Stroke Odysseys on those participating using mixed methods (interviews, observations and surveys) prior to and after each stage of the programme, and carry out non-participant observations during a percentage of the workshops, training and tour. This trial will also examine how effectively the programme is implemented and the factors (facilitators or barriers) that affect its implementation (i.e. implementation effectiveness). This will help us to identify not just 'if' but also 'why' the programme works and support our understanding of how it can be successfully delivered and scaled up within clinical pathways. Within this, the researchers will also explore the cost effectiveness of the programme, including the cost of its delivery and the balance of the benefit for the health sector, in order to be able to develop strong business plan for its longer-term use and wider scale implementation.
| Status | Recruiting |
| Enrollment | 122 |
| Est. completion date | November 1, 2022 |
| Est. primary completion date | November 1, 2022 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | Inclusion Criteria: - over 18 years of age - have had one or more stroke(s) - received inpatient care in a UK stroke care pathway and are able to follow a 2-stage command and hold a conversation in English if no supporter/friend is available to translate Exclusion Criteria: - any person with co-morbidities that would prevent participation in group activities e.g. dementia or deteriorating or fluctuating palliative conditions - unable to understand English - unable to commit to the 12-week programme |
| Country | Name | City | State |
|---|---|---|---|
| United Kingdom | Institute of Psychiatry, Psychology & Neuroscience | London |
| Lead Sponsor | Collaborator |
|---|---|
| King's College London | Kingston University and St George's, Rosetta Life |
United Kingdom,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | To evaluate emotional wellbeing, participation and activity of stroke participants and any change pre and post SO programme using qualitative methods | To evaluate emotional wellbeing, participation and activity of stroke participants and any change pre and post intervention - ethnographic research and interviews | The primary clinical outcome are qualitative changes in emotional wellbeing, participation and activity of stroke participants pre and post intervention (after 16 weeks) | |
| Primary | To evaluate to what extent Stroke Odysseys is acceptable, to survivors and wider stakeholders using the Acceptability of Intervention Measure (AIM) | The primary outcome implementation measure is acceptability as measured by the Acceptability of Intervention Measure (AIM) A 4-item measure of perceived intervention acceptability. Items are measured on a 5-point Likert scale (Completely Disagree-Completely Agree). Score is calculated mean. | The AIM will be collected during the workshop (Week 6), after the workshop is completed (Week 12) and after stroke ambassador training (Week 16). Interviews will be conducted after the workshop (Week 12) and after stroke ambassador training (Week 16). | |
| Primary | To evaluate to what extent Stroke Odysseys is acceptable, to survivors and wider stakeholders using semi-structured interviews. | The primary outcome implementation measure is acceptability as measured by semi-structured interviews to explore reasons for acceptability. | Interviews will be conducted after the workshop (Week 12) and after stroke ambassador training (Week 16). | |
| Secondary | To study the context, mechanisms and interactions which take place during Stroke Odysseys delivery | Non-participant observations of workshops | During workshop delivery (Week 6) | |
| Secondary | To explore learning and experiences of facilitators and participants | Semi-structured interviews (stroke participants and facilitators) | After the workshop is completed (Week 12) | |
| Secondary | To explore stroke survivors' preparation and participation in performances | Semi structured interviews (stroke participants) | Baseline | |
| Secondary | To evaluate to what extent Stroke Odysseys is appropriate to survivors and wider stakeholders | Intervention Appropriateness Measure (IAM) & Semi-structured interviews to explore reasons for appropriateness score.
The A 4-item measure of perceived intervention appropriateness. Items are measured on a 5-point Likert scale (Completely Disagree-Completely Agree). Score is calculated mean. |
The IAM will be collected during the workshop (Week 6), after the workshop is completed (Week 12) and after stroke ambassador training (Week 16). Interviews will be conducted after the workshop (Week 12) and after stroke ambassador training (Week 16).. | |
| Secondary | To evaluate to what extent Stroke Odysseys feasible to survivors and wider stakeholders | Feasibility Intervention Measure (FIM) & Semi-structured interviews to explore reasons for feasibility score The FIM is a 4-item instrument to assess perceived intervention feasibility. Items are measured on a 5-point Likert scale (Completely Disagree-Completely Agree). Score is calculated mean | The FIM will be collected during the workshop (Week 6), after the workshop is completed (Week 12) and after stroke ambassador training (Week 16). Interviews will be conducted after the workshop (Week 12) and after stroke ambassador training (Week 16). | |
| Secondary | To assess any unintended consequences of the programme | Semi-structured interviews | Interviews will be conducted after completion of the workshop (Week 12) and after completion of stroke ambassador training (Week 16). | |
| Secondary | To explore the facilitators and barriers to implementing the programme | Semi-structured interviews | Interviews will be conducted after completion of the workshop (Week 12) and after completion of stroke ambassador training (Week 16). | |
| Secondary | To explore the facilitators and barriers to sustained use of the programme | Semi-structured interviews | Interviews will be conducted after completion of the workshop (Week 12) and after completion of stroke ambassador training (Week 16). | |
| Secondary | To assess service utilisation and cost associated costs and changes in quality of life associated with the implementation of the programme | EQ5D-5L (quality of life measure) and AD-SUS (adult service receipt schedule) and semi structured interviews and activity data (to estimate implementation costs).
The EQ5D-5L is an instrument which evaluates the generic quality of life developed in Europe and widely used. The EQ-5D descriptive system is a preference-based HRQL measure with one question for each of the five dimensions that include mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. The AD-SUS measures the use of adult health services. |
These measures will be collected after completion of the workshop (Week 12) and after completion of stroke ambassador training (Week 16). | |
| Secondary | To explore the strategies including resource inputs utilised, used within individual sites to implement the programme | Semi-structured interviews | Interviews will be conducted after completion of the workshop (Week 12) and after completion of stroke ambassador training (Week 16). | |
| Secondary | To assess the adoption of the programme | Count the number of individuals delivering the programme, and the number of individuals supporting the programme (and continuing to do so) | This will be measured at baseline, after completion of the workshop (Week 12) and after completion of stroke ambassador training (Week 16). | |
| Secondary | To assess programme adherence and attrition rates | Data on the overall adherence to the programme, number of drops-outs and reasons why | Data recorded from register on weekly attendance rates for 12-week programme (stage 1) and for 4-week ambassador programme (stage 2) |
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