Ignite Creation Date:
2024-07-17 @ 11:53 AM
Last Modification Date:
2024-10-26 @ 3:33 PM
Study NCT ID:
NCT06476483
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-06-26
First Post:
2024-05-20
Brief Title:
Feasibility and Acceptability of Implementing DIALOG in a Psychiatric Rehabilitation Unit
Sponsor:
University of Sheffield
Organization:
University of Sheffield
Study Overview
Official Title:
Implementing the DIALOG Outcome Measure and a Solution-Focused Intervention DIALOG in a Rehabilitation Psychiatric Inpatient Setting A Mixed Methods Feasibility Study
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study aims to understand if implementing DIALOG in an inpatient psychiatric rehabilitation setting is feasible can the intervention be implemented and acceptable how the intervention is perceived by staff and patient participants If the intervention is proven to be feasible and acceptable a larger-scale study may take place This study has been developed in response to the trust-wide implementation of DIALOG outcome measures DIALOG offers additional solution-focused and person-centred follow-up questions to the DIALOG questions and links to multidisciplinary team MDT discussions It is hoped that the conversations had during DIALOG meetings will support positive outcomes and the learning gathered from this study will drive change and improvement for other people requiring psychiatric rehabilitation inpatient admissions in the future DIALOG has been successfully implemented in community settings in the national health service NHS but has not been implemented in psychiatric rehabilitation inpatient settings This study will aim to recruit patient and staff participants from NHS psychiatric rehabilitation inpatient wards Patient participants who will be eligible to take part are those who can consent are between the ages of 18-65 and can complete DIALOG and DIALOG To understand the feasibility of the intervention descriptive statistics will be collected and to understand acceptability focus groups will take place and surveys will be collected Quantitative data collection will take place over 5 months and will be split into 2 groups Group one will be a comparison group where participants will act as an extended baseline group and biweekly DIALOG outcomes will be collected Group 2 will be a Treatment group and participants will receive the DIALOG intervention intervention DIALOG outcomes will be collected biweekly as part of the intervention Finally there will be a period to gather qualitative feedback from patient participants using surveys and from staff participants using focus groups or semi-structured interviews
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None