Module - Co Production of Health (SBI123)
Aim of this module
Trainees completing this module will understand how patients, carers and the general public make use of health information individually, with peers and with healthcare professionals. The module will cover the context of health, care and wellbeing, including understanding the significance of the patient journey. The module will also cover technology, new innovations and other enablers of the co-production of health, including issues around access to and the availability of systems and information; skills development; access to or shared records (Personal Health Records); and communication (between doctor and patient or peer to peer). Consideration will be given as to how patients use information resources; models of ‘information needs’ and decision-making behaviour, including relevant studies on the quality of information online. Access to and availability of systems, including user interface and experience matters and the broader context relevant to these subjects – the changing nature of the clinician/patient relationship and the role of patient’s self-care – will be included. Additionally, the module will cover different paradigms for considering the role of the internet in healthcare, including internet interventions and ideas of ‘Web 2.0’, and will introduce m-health, the role of mobile health and other connected devices in healthcare. During this module, trainees will be expected to contribute to, write and deliver policy on the provision of information for patients/public and on patient/public-accessible systems. Trainees will be expected to apply and develop their knowledge and understanding of the patient perspective on the use and application of health informatics science within the health and social care context. This will include the key factors in the co-production of health and care between patients/public and healthcare services, and the role of technology in these relationships.
Work-based learning outcomes
Work-based Competencies
Learning outcome | Title | Knowledge | |
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1 | 1, 2, 3, 4, 5 | Apply information governance principles and best practice in the workplace, including confidentiality. |
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2 | 1 | Specify the essential components of an effective patient information/engagement strategy. |
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3 | 1 | Work with a clinical team and/or users to gain a wider view of the effectiveness of a patient information and engagement strategy, and design a solution to address any issues raised. |
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4 | 1 | Critically appraise a patient information/engagement strategy. |
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5 | 1 | Present your findings to colleagues and patients, making recommendations for revision of the patient information strategy. |
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6 | 2 | Design and carry out an audit of resources available for patients, ensuring any necessary approvals are in place. |
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7 | 2 | Analyse and interpret the data from the audit and prepare a written report, including an action plan and proposing solutions to any problems identified. |
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8 | 2 | Present the findings from the audit to an audience of peers. |
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9 | 2 | Work within the multiprofessional team, building and sustaining professional relationships. |
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10 | 3 | Specify the characteristics of effective online or electronic health resources. |
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11 | 3 | Design, document and undertake an evaluation of online or electronic health resources. |
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12 | 3 | Appraise the approach taken and document this and the conclusions of the evaluation for presentation to peers. |
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13 | 3 | Advise health professionals and patients making decisions about the use of electronic health resources for diagnosis and monitoring purposes. |
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14 | 4 | Write a proposal to enable you to meet with patients or patient groups to discuss their views with respect to a health informatics initiative and gain the necessary approvals. |
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15 | 4 | Apply an appropriate data collection method or methods. |
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16 | 4 | Analyse and present your conclusions to the owner of the initiative and to the survey’s participants. |
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17 | 5 | Critically evaluate a range of information/resources/internet/behavioural change apps and identify those that should be recommended to health professionals and patients, considering the underpinning evidence base. |
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18 | 5 | Interpret data to provide diagnostic and therapeutic advice to health professionals with respect to the appropriate use of information resources/internet interventions/behaviour change apps to support diagnosis and long-term treatment plans. |
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19 | 5 | Work with colleagues and within multidisciplinary teams to ensure information is used appropriately to formulate specific and appropriate management plans for patients using electronic health resources and, where appropriate, agreed timescales with the patient and colleagues. |
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Work-based assessment
Complete 3 Case-Based Discussion(s) | |
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Complete 3 of the following DOPS and/or OCEs | |
Type | Title |
DOPS | Undertake an audit of resources available to patients on a specific pathway |
DOPS | Compare and contrast local patient engagement strategy with others and discuss these with a patient engagement lead. |
DOPS | Investigate how patients experiences are collected and measured and present findings |
DOPS | Consider an information governance ethics request and detail your recommendations around this. |
OCE | Map the flow of information between healthcare professionals during a patient pathway or part of one for long pathways, noting how much flows via ICT, written notes, verbal communication and the patients experience |
OCE | Observe and present observations regarding the use of healthcare technology in a home environment, especially regarding barriers to its use |
OCE | Participate in an MDT meeting where the results of a clinical audit is discussed |