Stroke Nervous System Diseases
Conditions
Interventions
Four stroke services performing follow-up appointments will recruit a total of 96 participants, who are: stroke survivors within 7-months of stroke, aged 18 years and over, and attending their first f
completed sPCI and participants’ feedback on its use immediately after the appointment
participants’ satisfaction and empowerment within one-week of the appointment
and participants’ quality-of-life and use of health services three-months later. A selection of participants and staff will be interviewed about their experiences of the study.
Sponsors
University of Central Lancashire
Eligibility
Sex/Gender
All
Age
18 Years to 120 Years
Inclusion criteria
Inclusion criteria: 1. >= 18 years. 2. Experienced acute stroke within previous 7 months. 3. Attending first routine post-discharge stroke clinic appointment. 4. Able to complete sPCI, either themselves, with assistance for those physically unable to complete for themselves (e.g. have visual or motor problems), or by proxy for those without capacity to consent (i.e. relative/carer completes with their opinion of what the participant’s concerns are). 5. Able to communicate in English, or have a relative/carer willing to translate trial communications and materials for the participant, or able to use site-specific translation services, if available.
Exclusion criteria
Exclusion criteria: 1. Lack of capacity to consent themselves and no consultee assent available.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. The rate of completed sPCIs is measured using the number of sPCIs completed at the clinical follow-up appointment 2. sPCI use in consultation is measured using a participant's immediate feedback question on whether they recall the use of the sPCI in their consultation and audio recordings of consultations at clinical follow-up appointments and immediate feedback 3. Participant feedback on the use of sPCI is measured using an immediate feedback question on whether they recall the use of the sPCI in their consultation at immediate feedback 4. Patients completing sPCI is measured using the number of sPCIs completed at clinical follow-up appointments and process evaluation interviews 5. sPCI use during the consultation is measured using a participant's immediate feedback question on whether they recall the use of the sPCI in their consultation and audio recordings of consultations at clinical follow-up appointments and process evaluation interviews 6. Staff trained in sPCI use is measured using the number of staff trained during the training period and process evaluation interviews 7. sPCIs provided before the appointment are measured using the number of sPCIs sent to patients at the clinical follow-up appointment 8. Completed sPCIs available to staff conducting consultations are measured using data on consultation CRF about whether sPCI was available at the clinical follow-up appointment 9. Sites recruited are measured using the number of sites in the study at the end of the recruitment period 10. Participants recruited are measured using the number of participants recruited to the study at the end of the recruitment period 11. Eligibility rate is measured using screening logs at the end of the recruitment period 12. The recruitment rate is measured using screening logs and the number of participants recruited to the study at the end of the recruitment period 13. Retention/completion rates are measured using the number of completed 3-month questio | — |
Secondary
| Measure | Time frame |
|---|---|
| There are no secondary outcome measures | — |
Countries
England, United Kingdom
Outcome results
None listed