TY - JOUR AU - Patel, Dipen AU - Msosa, Yamiko Joseph AU - Wang, Tao AU - Williams, Julie AU - Mustafa, Omar G AU - Gee, Siobhan AU - Arroyo, Barbara AU - Larkin, Damian AU - Tiedt, Trevor AU - Roberts, Angus AU - Dobson, Richard J B AU - Gaughran, Fiona PY - 2024 DA - 2024/4/5 TI - Implementation of an Electronic Clinical Decision Support System for the Early Recognition and Management of Dysglycemia in an Inpatient Mental Health Setting Using CogStack: Protocol for a Pilot Hybrid Type 3 Effectiveness-Implementation Randomized Controlled Cluster Trial JO - JMIR Res Protoc SP - e49548 VL - 13 KW - blood sugar KW - CDSS KW - clinical decision support system KW - decision support KW - diabetes KW - diabetic KW - dysglycemia KW - electronic clinical decision support KW - hyperglycemia KW - hypoglycemia KW - implementation KW - medical informatics KW - mental health KW - mental healthcare KW - mental illness KW - metabolic health KW - randomized controlled trial KW - RCT AB - Background: Severe mental illnesses (SMIs), including schizophrenia, bipolar affective disorder, and major depressive disorder, are associated with an increased risk of physical health comorbidities and premature mortality from conditions including cardiovascular disease and diabetes. Digital technologies such as electronic clinical decision support systems (eCDSSs) could play a crucial role in improving the clinician-led management of conditions such as dysglycemia (deranged blood sugar levels) and associated conditions such as diabetes in people with a diagnosis of SMI in mental health settings. Objective: We have developed a real-time eCDSS using CogStack, an information retrieval and extraction platform, to automatically alert clinicians with National Health Service Trust–approved, guideline-based recommendations for dysglycemia monitoring and management in secondary mental health care. This novel system aims to improve the management of dysglycemia and associated conditions, such as diabetes, in SMI. This protocol describes a pilot study to explore the acceptability, feasibility, and evaluation of its implementation in a mental health inpatient setting. Methods: This will be a pilot hybrid type 3 effectiveness-implementation randomized controlled cluster trial in inpatient mental health wards. A ward will be the unit of recruitment, where it will be randomly allocated to receive either access to the eCDSS plus usual care or usual care alone over a 4-month period. We will measure implementation outcomes, including the feasibility and acceptability of the eCDSS to clinicians, as primary outcomes, alongside secondary outcomes relating to the process of care measures such as dysglycemia screening rates. An evaluation of other implementation outcomes relating to the eCDSS will be conducted, identifying facilitators and barriers based on established implementation science frameworks. Results: Enrollment of wards began in April 2022, after which clinical staff were recruited to take part in surveys and interviews. The intervention period of the trial began in February 2023, and subsequent data collection was completed in August 2023. Data are currently being analyzed, and results are expected to be available in June 2024. Conclusions: An eCDSS can have the potential to improve clinician-led management of dysglycemia in inpatient mental health settings. If found to be feasible and acceptable, then, in combination with the results of the implementation evaluation, the system can be refined and improved to support future successful implementation. A larger and more definitive effectiveness trial should then be conducted to assess its impact on clinical outcomes and to inform scalability and application to other conditions in wider mental health care settings. Trial Registration: ClinicalTrials.gov NCT04792268; https://clinicaltrials.gov/study/NCT04792268 International Registered Report Identifier (IRRID): DERR1-10.2196/49548 SN - 1929-0748 UR - https://www.researchprotocols.org/2024/1/e49548 UR - https://doi.org/10.2196/49548 UR - http://www.ncbi.nlm.nih.gov/pubmed/38578666 DO - 10.2196/49548 ID - info:doi/10.2196/49548 ER -