None listed
Conditions
Brief summary
A new allied health transdisciplinary stroke assessment was designed and implemented at the Mater Hospital Brisbane acute stroke unit (2020-2023), replacing time-consuming and separate stroke assessments completed by occupational therapy, physiotherapy, speech pathology, and social work. The new assessment process helped the allied health professionals to streamline stroke services, saving assessment time and reducing occasions of service required to meet clinical and service goals and safely discharge patients from hospital. The proposed study is the translation phase of the work. The aim is to modify and implement the transdisciplinary stroke assessment in other settings, test if similar results can be achieved, and understand what factors drive success. The hypothesis states that compared to separate stroke assessments, the new transdisciplinary assessment will reduce allied health stroke assessment time by at least 35 minutes per patient in the initial occasion of service. This study has the support of the Queensland Chief Allied Health Officer.
Interventions
Transdisciplinary Initial Neurological Screening Assessment (TINSA): The TINSA is an assessment which combines assessments and tasks of routine physiotherapy, occupational therapy, social work, and speech pathology assessments. It has replaced discipline-specific assessments (occupational therapy, physiotherapy, speech pathology, and social work) at the Mater Hospital Brisbane, and acts as a trigger for referrals to allied health professionals. The TINSA has been tested by a clinical pre-/post- study at the Mater Hospital Brisbane, and results showed improved time-efficiency and cost savings without affecting the quality of care (patient safety and outcomes). The TINSA is administered by a trained occupational therapist or physiotherapist. For patients receiving the TINSA, this involves verbal questions, a brief communication screen and a physical assessment (including a mobility assessment). When the TINSA is used, patients will experience less duplication of assessment questions and tasks. After the assessment, the administering allied health professional (e.g., occupational therapist or physiotherapist) will make referrals to the wider Allied Health team, as per their clinical training and judgement. After the novel TINSA has been administered and subsequent allied health referrals made, allied health input (i.e. the treatment, re-assessment, discharge panning, follow-up) will continue as per usual care. If no further allied health is indicated after the TINSA, the assessor can discharge the patient (i.e. safe to return home). In this study, the TINSA will be modified (as necessary to suit the local setting) and implemented in the study sites, replacing discipline-specific allied health assessments. At each site, a clinical pathway will be developed, as a strategy to ensure adherence to the intervention. The TINSA will be used for all patients admitting during pre-determined time periods at each study site (during the 2 week transition period, and the post-implementation period). Usual allied health assessment will be used for all patients during the pre-implementation period. Competency training for the TINSA: 9 eLearning modules are available to health professionals via the Queensland Health learning management system (iLearn). The training modules provide information on how to perform tests, asks questions, and clinical reasoning across the domains of vision/perception, communication assessment, respiratory assessment, mood, upper/lower limbs assessment, shoulder precautions, functional mobility assessment, Timed Up and Go test, and the 10 meter walk test. Each module includes written information, videos on task/question administration, and a knowledge check quiz. These resources were developed as part of an earlier study that evaluated the TINSA at the Mater Hospital Brisbane (ACTRN12621000380897). The resources have now been transferred onto iLearn and are available for Queensland Health and external professionals. The designated allied health professional/s (e.g., occupational therapists and physiotherapists) complete the competency training before administering the TINSA with patients. The modules take approximately 10-30 minutes each and are completed when the professional is able. In the study, a 2 month transition period will be used to allow for sufficient time to complete the training. After completing the eLearning modules, the allied health professional will complete the TINSA under supervision until they are marked as 'competent' according to the competency assessment criteria (copy available online: https://doi.org/10.14264/1749adb, pp80-81). The training can be re-completed at any time, at the discretion of the allied health professional, to ensure maintenance of skills. The mandatory competency training is a strategy to ensure the TINSA is delivered in a safe and standardized way. Implementation manual: An implementation manual for transdisciplinary approaches in healthcare was developed following a previous study (ACTRN12621000380897) and is available online https://doi.org/10.14264/1749adb. The implementation manual will guide the local team to modify the TINSA to suit their local setting and patient presentations. The implementation manual involves three stages to 1) plan and prepare, 2) implement and evaluate, and 3) sustain and expand. In this study, stages 1 and 2 will be followed during weekly team meetings prior to the implementation of the TINSA. Focus Group (healthcare providers): At the end of the transdisciplinary implementation and data collection phase, acute stroke unit/medical ward staff will be invited by the local study coordinator to participate in a once-off, online, 60 minute Focus Group (via work email, staff meetings/huddles, and verbal invitations). Recruitment will occur over two weeks at each study site. It is estimated that a maximum of 20 staff will be asked to participate (i.e., all allied health, nursing, medical staff working on the ward). Interested staff will reply and nominate a suitable date/time. We are aiming to recruit a maximum of 8 Focus Group participants per site. At this point, the local study coordinator will organise the Focus Groups by sending Outlook diary invitations with a Zoom link for the Focus Group and the PICF for healthcare staff to read and consider before providing written consent. The Principal Investigator (AM) will facilitate and later transcribe the online Focus Group with healthcare staff. A Co-investigator (LL) will assist with the Focus Group. The role will be to alert the Principal Investigator of any matters that may not have been noted by the focus group facilitator and which need to be addressed before the end of the Focus Group; and to take notes of any non-verbal or other matters that may arise. This method will ensure that the Focus Group method obtains its aims and objectives. In the focus group, topics discussed will be the utility of the TINSA and the implementation experience.
Sponsors
Study design
Eligibility
Inclusion criteria
1) Working party members will include the local study coordinator who invites other staff to join if they are: • Clinical healthcare professionals working on the acute stroke unit/medical ward during the study period • Clinical managers of staff involved in the study • Other staff employed at the study site with local/expert knowledge to contribute (e.g., education specialists, clinician-researchers, stroke specialists) 2) Patient/carer consumers are eligible to provide feedback on the transdisciplinary assessment and study results if they: • Have experienced stroke assessment as a hospital inpatient or carer, at any Queensland hospital. For example, consumers could be current/previous patients, carers, or consumer representatives. • Be able to use technology independently or with carer assistance (i.e., access/watch/listen to a video and read/respond to online survey questions) • Attend for 2 sessions of 60-90 minutes (with breaks if required) • Understand/read/write in English • Consumers will not require training to participate and can be supported by a carer. 3) Patients with stroke/medical conditions are eligible to participate if they: • Admit to the participating acute stroke unit/medical ward with confirmed/suspected stroke (acute stroke unit) or a medical condition (medical ward) during the study period and business hours (i.e., Monday–Friday) • Receive allied health assessment/s • A third-party interpreter is available when patients do not speak English • Have not previously been included in the study 4) Healthcare staff are eligible to participate in the focus group if they: • Have worked on the participating acute stroke units or medical ward during the study period • Have worked in a clinical role, clinical manager role, working party member, and/or local study facilitator role during the study period.
Exclusion criteria
Patient exclusion criteria: • Patients who are admitted over a weekend (Saturday and Sunday) or on a public holiday. • Patients with stroke who are not transferred to the Acute Stroke Unit or medical ward. • Patients who do not speak English where a third-party professional interpreter is unavailable to assist with translation. • Patients who have already been included in the study at an earlier time point (i.e., have been readmitted). • Patients without cognitive capacity to provide consent (criteria for Hollywood Private medical ward only)