Study setting {9}
Recruitment of people with ABI will take place between November 2019 and June 2020 in three hospitals in the Netherlands: Deventer hospital (Deventer), St. Antonius hospital (Nieuwegein and Woerden) and Flevo hospital (Almere). Hospital staff will recruit people with ABI without further involvement in the study procedures, assessments will take place through home visits, via telephone or by sending questionnaires via mail.
Eligibility criteria {10}
People with ABI
People with ABI are eligible for the trial if they comply with all of the following criteria at hospital discharge:
- Acquired brain injury objectified by medical specialist (meningitis, encephalitis, hydrocephalus, subarachnoid haemorrhage, intracerebral or intracranial haemorrhage, ischemic stroke, transient ischemic attack, concussion, contusion, other head trauma).
- Aged 18 years or older.
- Living in the community prior to the injury.
- Discharged home or to a rehabilitation centre after hospital visit/admission.
- Sufficient command of the Dutch language to understand study procedures.
- Access to a computer and the internet (to use the monitoring tool, ).
- Willing and able to give informed consent.
Exclusion criteria for people with ABI are:
- A neurodegenerative disorder such as Parkinson’s disease or dementia (because of the progressive course of the disease).
- A diagnosis related to neuro-oncology (since an intensive care trajectory is already in place for this group).
- Discharge to a nursing home.
Family members
Family members are eligible when they comply with all of the following below. Off note, we speak of family members since usually the partner, a child or a parent is most likely to be the primary caregiver in case the person with ABI needs support, but friends or neighbours can also participate in this role if they are the ones most close to the person with ABI.
- The person with ABI is eligible and willing to participate (i.e. family members can only participate if their relative with ABI is participating).
- They are (or would be if necessary) the primary informal caregiver; i.e. the person most close the person with ABI.
- Aged 18 years or older.
- Sufficient command of the Dutch language to understand study procedures.
- Access to a computer and the internet (to use the monitoring tool and questionnaires).
- Willing and able to give informed consent.
Case managers
Health care professionals are eligible for the role of case manager if they have professional experience in caring for people with ABI at bachelors’ level or higher (e.g. social workers, nurses, speech and language therapists, occupational therapists, etc.,). They need to be available for at least 4-8 hours per week for the duration of the project, willing to participate in the case manager training at the beginning of the project and in the monthly supervision meetings, and willing to register and document their case manager activities and experiences for research purposes. A formal application procedure will be followed; candidates are hired based on their resume, motivation and job interview by the project leaders.
Who will take informed consent? {26a}
People with ABI and family members who are willing to participate will be visited at home by a trained research assistant, who will obtain informed consent prior to baseline assessment and after going over the study procedures. In case the home visit cannot take place, study procedures will be explained over the phone and informed consent is obtained by mail.
Additional consent provisions for collection and use of participant data and biological specimens {26b}
Not applicable.
Interventions
Explanation for the choice of comparators {6b}
Case management is compared to care as usual because it is expected to have higher levels of continuity, accessibility, a wider range of care/support options and better timing, which could lead to faster recognition of brain injury-related problems, shortening searches for good information and access to adequate support.
Intervention description {11a}
Case management
The framework
The framework for case management for ABI was developed based on a combination of the taxonomy for case management for brain injury [24] and descriptions of case management for dementia in the Netherlands (e.g. [33–46]), because this form of case management is reasonably well integrated in the Dutch health care system. Such services can serve as a base for care innovations for people with ABI because of the shared focus on supporting people to adapt to the consequences of a disorder or disease in daily life [47].
Case management aims to support people with ABI and family mambers’ self-management of the consequences of ABI and psychosocial well-being, to prevent (escalation of) problems, and to facilitate timely access to appropriate services. We propose the following case management elements:
- Monitoring: tracking functioning and well-being of people with ABI and family members. In the present study, a digital monitoring system is used for this purpose (described below).
- Identification: identification of questions, problems and needs (based on monitoring) that hinder functioning and well-being at the time they emerge.
- Assessment: assessing the nature and severity of the presented problem, burden on and capabilities of the person with ABI and the family member, the role of their social network, making implicit or unmentioned questions and problems explicit, drawing conclusions about the core problem in the individual context.
- Information (psycho-education): providing information and education on the (impact of) ABI to assist understanding, information or education related to the question or problem (with a focus on capabilities to self-manage the problems), informing on available care and support services.
- Provision of support: guiding decision-making with regard to managing the problem, providing practical or psychosocial support for relatively mild problems (focused on maintaining or improving self-management).
- Referral: referring to more specialized care or support for relatively complex problems and guiding decision making with regard to what available services to use.
- Coordination: supporting access to services, facilitating collaboration between different service providers and bringing about appropriate care when this is not available through the regular services.
Case management is person-cantered and supposed to follow the 'stepped care' and ‘matched care’ principle, starting with the least complex form of care and support that meets the demand for help (stepped care), with the form and intensity individually built around the needs and capabilities of the person with ABI and/or the family member (matched care). Case manager activities may therefore vary from offering a listening ear or providing information and advice, to intensively coordinating longer-lasting specialist care. Case manager involvement also may vary in intensity over time, ranging from only monitoring to more intensive involvement.
Case management activities are community-based; they will take place at peoples’ home or other relevant places such as at work, or over the phone, via video calls or via email. While following the stepped care principle, case managers are flexible in the actions (interventions) they choose based on their own professional expertise, the links they make with available services (e.g. they are independent) and the way they create support when available services do not match people’s needs. Part of this study is mapping actual case manager activities onto the proposed elements and exploring whether this concept should be adjusted based on case manager and participant experiences, in order to move towards a more detailed description of what these elements entail in practice.
Monitoring tool (the ReMinder)
Participants receiving case management will be entered into a digital monitoring tool, called the ReMinder, developed by authors KHMJ and MD. This tool was originally developed to empower people who leave the hospital after a head trauma or stroke and their family to find information and get easy access to care in case of the development of problems caused by the injury on the long term. In the current research project ReMinder is incorporated within OZO Verbindzorg, an online communication system that links different service providers through an online platform, depending on what professionals are allowed to have access to (parts of) this system as indicated by the participant. Each participant signs an agreement in which both OZO and the participant determine which data about the person with ABI are being entered and used by whom; this is all conducted according to the prevalent laws for personal data and privacy.
People with ABI and family members, each having their own account, will automatically receive an email every three months, which allows them to enter the monitoring system and to answer two questions: 1) Do you experience problems as a consequence of brain injury? 2) Are you (Is your loved one) able to do all the things you were (he/she was) doing prior to the brain injury? Both questions can be answered with yes or no. If the participant responds ‘yes’ to question 1 and/or ‘no’ to question 2, they are directed to a 32-item questionnaire asking about functioning in the areas of health, daily life, activities, social contacts and consequences of ABI, This questionnaire was composed by the developer of the ReMinder (authors KHMJ and MD), inspired by the Checklist for Cognitive and Emotional Consequence of Stroke (CLCE-24 [48]), the Utrecht Scale for Evaluation of Rehabilitation-Participation (USER-P [49]), Outcome Questionnaire (OQ-45 [50]) and the life domains of the ICF: International Classification of Functioning, Disability and Health (ICF-model). Participants fill out the questionnaires as self-report, family members fill out the questionnaire reporting about the person with ABI, and fills out five extra questions about his or her own well-being. In order to facilitate easy access to the case manager, at completion of the 32-item questionnaire participants will be asked if they would like to have contact with the case manager (yes/no). In addition, people with ABI and family members also have the opportunity to ask a question to the case manager directly at any time within the online environment.
The responses are visible to the case manager to keep track of functioning and well-being of the person with ABI. The case manager will contact those participants who explicitly indicate that they would like to get in touch. For participants who do not initiate contact with their case manager themselves, the case manager determines whether to contact the participant after the second time participants have filled out the ReMinder (i.e. three months after the first ReMinder questionnaire). The decision to get in touch with the participant will generally be based on whether responses indicate that certain problems haven’t been resolved (consistently low scores in one or more areas), a deterioration in scores, or profound discrepancies in scores between the person with ABI and their family member.
The case manager
The case manager is a fixed contact person; building a relationship is desirable because of the complexity of learning to live with ABI within the individual context, and to prevent the person with ABI and their family from having to tell their story over and over again. A back-up case manager will be assigned as well, who will be involved when the primary case manager is unavailable and who can serve as a sparring partner for the primary case manager.
The case managers form three teams, one in each region. Teams are composed of professionals from different disciplines and with varying backgrounds; some have been working in clinical/rehabilitation settings, others in community outreach, and their experience with support and treatment approaches may be focused on cure or on care. Two of the teams include a peer support worker.
Case managers will participate in a 4-day training prior to the start of the study. The training has a coaching character, promoting team members to draw upon each other’s knowledge and experience. During the training, case managers learn to see beyond one’s own specific professional discipline, get to know the professional background of the other team members and are coached in learning from each other to best support people with ABI and their family. Regular supervision meetings are organized with case managers within regions at least every two months, and between regions twice a year.
Care as usual
The usual care differs depending on the regional structures and collaborations. In all regions, limited structured care is available for people who suffered a stroke, mostly for secondary prevention purposes, with a limited duration of 1 year. No structural care is provided for other types of ABI. People with ABI can make use of different forms of care that may or may not involve professionals with expertise on ABI, such as physiotherapy, occupational therapy or social work, but patients usually need to take initiative to find and access these services either themselves or through their general practitioner.
Criteria for discontinuing or modifying allocated interventions {11b}
By design, case management is a modifiable form of care, as it is about organizing interventions based on the individuals’ needs, strengths, weaknesses and living situation. As described before, this study is of a pragmatic nature, granting case managers the flexibility to act as they see fit to support participants, while providing the least amount of support necessary to stimulate self-management.
Complete discontinuation of case management will occur on participants’ request. People with brain injury can continue if their family member wishes to stop. Off note, a form of ‘active discontinuation’ occurs when participants do not need any support at a given moment: case managers will then monitor the participants’ well-being via the ReMinder and will be available when questions or problems do occur, but do not reach out otherwise.
Strategies to improve adherence to interventions {11c}
The ReMinder serves as the basis for case managers to monitor if support is needed; participants will receive reminder emails twice a week until they open the ReMinder questionnaire. When two consecutive ReMinder questionnaires (i.e. three months apart) are not filled out, participants will be asked by email whether they have trouble getting access to the system, with filling out the questions or whether there is another reason for not using the ReMinder. If they do not respond to any of these emails, their case manager will reach out to explore the reason for this and to determine if further case manager activities are required. Other elements of case management are not subject to adherence as such.
Relevant concomitant care permitted or prohibited during the trial {11d}
All participants are allowed to receive any form of care that they need. Service use will be measured with a questionnaire. Participants are asked not to participate in any other studies concerning psychosocial or pharmacological care for the duration of this trial.
Provisions for post-trial care {30}
Depending on the results of the study and available funding, case management will be continued or gradually scaled down. In case of continuation, participants in the control condition will have the opportunity to receive case management after the study period.
Outcomes {12}
Feasibility
Feasibility will be assessed using the process evaluation framework of Saunders, Evans and Joshi [51]. This involves mapping fidelity (quality), dose delivered (completeness), dose received (exposure), reach (participation rate), recruitment (procedures, maintenance of participant involvement) and context (aspects of the physical, social, and political environment).
Effectiveness
Outcomes for people with ABI
Outcomes measures were chosen according to the aim of case management, which involves the concepts of psychosocial well-being, self-efficacy and (unmet) needs.
Psychosocial well-being will be assessed using the Hospital Anxiety and Depression Scale (HADS [52]), the Utrecht Scale for Evaluation of Rehabilitation-Participation (USER-P [49]) restriction subscale and the Life Satisfaction Questionnaire (LiSat [53]). The HADS will serve as the primary outcome measure and will be administered to assess symptoms of anxiety and depression. The scale consists of 14 items scored on a 4-point scale ranging from 0 to 3 with varying anchors. Total scores can be calculated for two subscales (anxiety and depression); subscale scores of >7 suggest the presence of an anxiety disorder or depression. The psychometric quality of the scale is sufficient [54]. The USER-P restriction subscale consists of 9 items asking about restrictions in vocational, leisure and social activities as a consequence of ABI. Items are rated on a scale from 0 (not possible) to 3 (without difficulty) and a ‘not applicable’ option. The total score ranges from 0-100 based on the number of applicable items; higher scores indicate less restrictions in participation. The scale has shown sufficient reliability and validity [49]. The LiSat assesses various aspects of life satisfaction including life as a whole, self-care management, contacts with friends, vocational, family life, partner relationships, financial situation, leisure situations and sex life. The nine items are scored on a 6-point scale ranging from “very dissatisfied” to “very satisfied”. The scale has satisfactory reliability and validity [55,56].
The concept of self-efficacy, one’s confidence in the ability to deal with (health) problems, will be measured as a proxy for self-management, since self-efficacy is a prerequisite for behavioural change. Self-efficacy will be measured with the Patient Activation Measure (PAM [57]), which is a 13-item instrument assessing self-reported knowledge, skills and confidence for self-management of one’s health or chronic condition. Items are scored on a scale of 0 (disagree strongly) to 4 (agree strongly) and a not applicable option. An algorithm is available to transform the scores on the PAM to different levels of self-management, from ‘disengaged and overwhelmed’ to being their own health advocate. The PAM requires a license and sharing of the de-identified data with Insignia Health. The Dutch version of the PAM has shown good internal consistency (Cronbach’s alfa .88), moderate to strong item-rest correlation and moderate test-retest ability [58].
Care needs will be assessed with the Longer-term Unmet Needs after Stroke questionnaire (LUNS[59]). The LUNS consists of 22 items scored with ‘yes’ or ‘no’ and one open ended question on the physical, social, and emotional consequences of stroke. To make the LUNS applicable for people with other types of brain injury, we replaced the word ‘stroke’ by ‘brain injury’ in two items. A validation study of the Dutch version of the LUNS concluded that the scale is reliable and valid [60]. It should be noted that some items merely express worries or a problem rather than needs (e.g., “I am worried that I might fall [again] and this is stopping me from doing my usual things”). Nevertheless, we consider the scale to be the most comprehensive scale to assess care needs in the ABI population available in Dutch.
Family member outcomes
Psychosocial well-being, self-efficacy and (unmet) needs will also be measured in family members. In addition to the HADS and LiSAT, of which a description is provided above, caregiver burden will be assessed within the concept of psychosocial well-being. The Caregiver Strain Index (CSI [61]) will be used, which consists of 13 items that can be responded to with ‘yes’ or ‘no’ and total scores ranging from 0-13; higher scores reflecting higher caregiver burden and substantial burden is indicated by a score of 7 or higher. For people who suffered from stroke, the CSI is the most commonly used scale and recommended in the Dutch stroke care guidelines [62] and the scale has shown sufficient validity and reliability [63].
Self-efficacy will be assessed using the Carer Self-Efficacy Scale (CSES) [64]. The CSES measures self-efficacy with regard to care management and service use, each in 5 items on a 10-point scale from ‘not at all certain’ to ‘very certain’; higher scores on the CSES indicate higher levels of self-efficacy. Reliability and validity of the scale are sufficient [65].
Family members’ needs will be assessed with the Family Needs Questionnaire (FNQ [66]). The scale includes 40 items assessing needs that may arise during acute rehabilitation, soon after discharge, and in the long-term after ABI. Subscales include health information, emotional support, instrumental support, professional support, community support network, and involvement with care. Family members are asked to indicate the importance of each perceived need and then rate the degree to which the need has been met. The Dutch translation has shown sufficient reliability [67]. Information on the validity of the translation is not yet available, but the English version has shown to be valid [68].
Cost-effectiveness and cost-utility
Cost-effectiveness and cost-utility will be determined using the EuroQol (EQ-5D-3L) and a service use questionnaire. The EQ-5D-3L [69] consists of five questions measuring health status. The dimensions covered are mobility, self-care, daily activities, pain or discomfort, and anxiety or depression. These domains are rated as ‘no problem’, ‘moderate problem’ or ‘unable to do’. The EQ-5D-3L has shown good measurement properties [70]. Service use will be measured with a self-report cost-questionnaire, which was constructed to collect cost data from a societal perspective. It is based on the steps described by Thorn and colleagues [71] and on the questionnaire used by Rauwenhoff and colleagues [72].
Other study parameters
The following demographic and injury related characteristics will be collected: date of birth, gender, education, date of most recent ABI, type of most recent ABI, date and type of previous ABI(s), hospital admission (yes/no), length of hospital stay of most recent ABI, referral destination at hospital discharge (home or rehabilitation centre).
Participant timeline {13}
The schedule of enrolment, interventions and assessments can be found in Table 1. All participants will receive the study questionnaires every six months until December 2021. Depending on the time of inclusion (up to June 2020), people with ABI will be followed up for 18 to 24 months. A subsample of people with ABI and family members will be approached for additional participation in focus group interviews, taking place at the end of the study (between October and December 2021).
Sample size {14}
Power calculation was based on the primary outcome measure Hospital Anxiety and Depression Scale (HADS). A study evaluating a monitoring/psycho-educational intervention in patients with possible ABI due to cardiac arrest showed to be effective in improving both anxiety and depressive symptoms with a group difference on the HADS of 3.25 points, corresponding to a Cohen’s d effect size of 0.36 [73]. With an alpha of .05 and power value of 80%, a sample size of 194 is required to detect such between-group effect in the post-intervention measurement. This number can be adjusted for the correlation between baseline and follow-up data, since baseline measures will be entered in the model as an independent variable, by multiplying the sample size by 1-R2 (R is the population correlation between the dependent variable (post-intervention) and the pre-intervention measurement) [74]. R is estimated to be at least 0.5, making the sample size 194*(1-0.52) = 146. Taking a drop-out rate of 30% into account, at least 209 people with ABI should be recruited. For each participating person with ABI, the family member who is or would be acting as the informal caregiver will be asked to be enrolled in the study as well. The number of participating family members will not exceed the maximum of 209.
Recruitment {15}
All people who have visited or were admitted to the emergency department or neurology department of three hospitals in the Netherlands (Deventer hospital, St. Antonius hospital, Flevo hospital) between November 2019 and June 2020 will be considered for participation. At each hospital, trained hospital staff will use the electronic patient files to select possible eligible people with ABI based on the inclusion criteria. The staff will call these people with ABI within two weeks after they left the emergency room/neurology department. The hospital staff will then explain the aim of the study and the study procedures, screens for eligibility and asks whether a family member is present. When the person with ABI or person with ABI-family-member couple are eligible and interested in participation, the hospital staff will send them the participant information letter and asks permission for them to be contacted by the researcher. The researcher will call after a week to clarify any questions they may have. If they are interested in participating, an appointment will be scheduled with the research assistant to sign informed consent by both the person with ABI and the family member, complete the baseline assessment and perform the randomization. In case the person with ABI is referred to inpatient rehabilitation, the appointment will take place as soon as possible after they are discharged home from the rehabilitation centre.
Assignment of interventions: allocation
Sequence generation {16a}
Participants (people with ABI or people with ABI-family-member couples) will be randomly allocated with a 1:1 ratio to either the case management group or the care as usual group, using a computerized random schedule, in blocks of six. The randomization block size will not be disclosed to the research assistant who enrols and assess participants, to ensure concealment.
Concealment mechanism {16b}
The research assistant will be provided with sequentially numbered, opaque sealed envelopes containing randomization information. The research assistant will follow the sequence and open the envelope after baseline assessment is completed.
Implementation {16c}
The allocation sequence will be generated by a person who is not involved in the study assessments, using a computerized random number generator (www.random.org/lists/). This person will prepare sequentially numbered opaque envelopes containing the information about the group assignment of the participant and seal and the envelopes. The research assistant, who is blind for the allocation sequence and block size, will enrol participants, open the envelope after baseline assessment is completed and provide participants with the information about treatment allocation.
Assignment of interventions: Blinding
Who will be blinded {17a}
At baseline assessment, group allocation will be unknown to both the research assistant and the participants; treatment allocation takes place after completion of the baseline assessment by a research assistant. If people with ABI wish to be visited at home for the follow-up assessments rather than receiving the questionnaires via mail, they will be visited by a member of the research team who is blind to their treatment allocation. Blinding is not possible for the assessment of feasibility.
Procedure for unblinding if needed {17b}
There are no foreseen circumstances under which unblinding is necessary.
Data collection and management
Plans for assessment and collection of outcomes {18a}
Feasibility
Several methods will be used to obtain information on the process evaluation outcomes: 1) registration forms for case manager activities, 2) written notes of supervision meetings, 3) responses to the questionnaires and participants’ communication with case managers derived from the ReMinder and the OZO system 4) evaluation forms for participants (both people with ABI and family members) receiving case management, and 5) focus group interviews.
Focus groups
At the end of the study period, focus groups will be held to obtain in-depth information on the experiences with receiving case management (for participants) and with delivering case management (for case managers). Focus groups are group interviews (approximately 6 participants each) with a particular subject (or focus), and they make use of social interactions between participants. Focus groups are an ideal method to reveal various perspectives on a topic and to uncover new insights and unanticipated issues [75]. During the focus groups, a moderator (researcher) will use a discussion guide that will include questions on the topics based on fidelity, dose delivered, dose received, reach, recruitment and context [51]. The interviews will be audio recorded as well as video recorded, to ensure identification of potentially relevant non-verbal information or cues presented by the participants. A second researcher will take additional notes during the focus group interviews.
People with ABI and family members of the three different regions will be selected to form a sample including a wide range of injury-related characteristics and needs (purposively selected) to participate in focus group interviews at the end of the study period. In each region, one people with ABI focus group and one family member focus group will be planned (six in total). This should be sufficient to achieve saturation, i.e. that no new issues around emerge from the focus group interviews, as research suggests that saturation is usually achieved after the fourth group discussion [75]. Saturation will be checked after these groups and if necessary, additional focus groups will be planned. Because the case managers form a limited group within the scope of the project (25-30 case managers), we aim to include all case managers in focus groups, divided in 3-4 groups.
Effectiveness and cost-effectiveness
The baseline assessment will be completed no more than two months after the visit to or discharge from the hospital or, in case of inpatient rehabilitation following hospital discharge, as soon as possible after they leave the rehabilitation centre. Ideally, assessments take place at the participants’ home, but can take place via telephone or questionnaires may be sent and returned by mail in case home visits are not possible (on time). A trained research assistant will explain the study procedures once more and collect the consent form. During home visits, participants fill out the questionnaires on their own and have the opportunity to ask questions. The research assistant will provide support when necessary, for example by reading the questions and possible answers out loud in case of reading difficulties (a common problem after stroke). Information on gender, educational level and living situation will be collected at baseline; date of birth, type and date of most recent and previous brain injuries and discharge destination will be drawn from hospital records by hospital staff. Follow-up measurements will be mailed to the participants, unless people prefer to be assisted, in which case a research assistant (blind to treatment allocation) will visit them at home. For the case management group, the 12-month and the final assessment (18 or 24 months) will include an evaluation form with regard to case management for those in the case management group (separately assessed when people are visited at home to ensure blinding of the research assistant) and ReMinder responses and communications will be drawn from the online system (OZO).
Plans to promote participant retention and complete follow-up {18b}
Participants will receive a five-euro gift card for each measurement (maximum of 25 euros for the complete study). For participating in the focus groups, they will receive an additional fee of ten euros (gift card).
Data management {19}
Data will be collected on paper and then entered electronically twice by members of the research team; any discrepancies between the two entries will be resolved by the person responsible for the second entry, or by discussion with a third researcher if necessary. There are restrictions in place for entering questionnaire data based on the range of answers. Manual range checks will be performed for demographic information. An audit trail will provide with information on all activities in the electronic database. Access to electronic data is controlled by a password system, access to original data will be restricted by storing the data in a locked cabinet (see Confidentiality).
Confidentiality {27}
Data will be handled confidentially and reporting will be coded. All participants will receive a unique identifier that cannot be used to link the data to an individual subject (i.e. CM001). Collected data and personal information will be stored separately in locked cabinets. The involved researchers from Maastricht University will safeguard the key to the code. Only the national supervisory authorities such as the Inspection for Healthcare and Youth (in Dutch: Inspectie voor Gezondheidszorg en Jeugd) will have access to the data upon request. The handling of personal data will comply with the EU General Data Protection Regulation (GDPR) (in Dutch: AVG), the Dutch Act on Implementation of the General Data Protection Regulation, and the Research Data Management Code of Conduct of Maastricht University. The data will be stored for 15 years after the end of the study.
Plans for collection, laboratory evaluation and storage of biological specimens for genetic or molecular analysis in this trial/future use {33}
Not applicable.
Statistical methods
Statistical methods for primary and secondary outcomes {20a}
Feasibility
Registration forms, evaluation forms and written notes of supervision meetings will be analysed descriptively in terms of fidelity, dose received, dose delivered, reach, recruitment and context. Focus groups will be analysed qualitatively. Audio and videotapes of all focus group interviews will be transcribed verbatim. Analyst triangulation will be applied [76]; the transcripts and observations combined with additional notes that will be taken during the focus group interviews will be analysed independently by two researchers using the qualitative analysis software ATLAS.ti (version 7.0). An inductive content analysis approach will be adopted [77], in which common themes and categories emerge using inductive reasoning and constant comparison. The texts will be thoroughly read and open codes will be applied to describe all aspects of the content [78]. Codes referring to the same phenomenon will be grouped into categories and these categories will be grouped into higher-order themes. Categories and themes will be combined into general statements to describe the phenomenon [77]. Discrepancies in coding and interpretation will be discussed in a meeting together with a third researcher to reach consensus regarding the categories and themes. The video recordings will be compared with the written transcripts to be able to identify potentially relevant additional non-verbal information or cues presented by the participants. Saturation will be established when no additional categories or themes emerge after the planned focus group interviews. Quotations will be selected based on representativeness of the emerged themes by the coordinating researcher and verified by the other two researchers.
Effectiveness
Multilevel modelling will be used to assess the improvement of case management participants over time compared to care as usual. We will enter time, group and their interaction as fixed terms. Separate analyses will be performed to assess 24-month outcomes for the subgroup of participants for whom this data is available. The resulting models will be extended with covariates, controlling for the effects of age, gender and level of education. Moreover, interactions between covariates and condition and the time predictor will be included. The main effects and interactions will be kept in the model as long as they contribute significantly to the model. Significance of the fixed regression effects will be tested using the appropriate t-test (a = .05).
Cost-effectiveness and cost-utility
The trial-based economic evaluation will involve a combination of a cost- effectiveness analysis (CEA) and a cost-utility analysis (CUA). Effects will be presented as clinical outcomes (i.e. self- efficacy and psycho-social well-being). In these CEAs, the incremental cost-effectiveness ratio (ICER) will be expressed as the incremental costs per point improvement on the primary outcome measure. The primary outcomes measure for the CUA will be QALYs (quality adjusted life years), based on the EuroQol (EQ-5D-3L). The EQ-5D-3L can distinguish between different health states. For each of the different states a weight is contributed based on the valuation given by the general population (Euroqol-Group). These range from 0 (representing death) to 1 (representing full health). Cost-effectiveness evaluations make use of these utilities. In the CUA, the ICER will be expressed as the incremental costs per QALY. This economic evaluation will be performed from a societal perspective, which implies that all relevant costs and outcomes will be considered. The time horizon will be the same period as the follow-up period of the trial.
Total costs will be estimated using a bottom-up (or micro-costing) approach, where information on each element of service used is multiplied by an appropriate unit cost and summed to provide an overall total cost. The economic evaluation will assess not only the intervention costs, but also healthcare costs, patient and family costs, and costs outside the health care sector. For this study we have developed a cost questionnaire, based on existing questionnaires which will identify all relevant costs aspects.
Despite the usual skewness in the distribution of costs, the arithmetic means will be generally considered the most appropriate measures to describe cost data. In case of skewness of the cost data, non-parametric bootstrapping will be used to test for statistical differences in costs between the case management and care as usual group. The bootstrap replications will be used to calculate 95% confidence intervals (CI) around the costs (95% CI), based on the 2.5th and 97.5th percentiles. If cost data are distributed normally, t-tests will be used. The robustness of the ICER will be checked by non-parametric bootstrapping (1000 times). Bootstrap simulations will also be conducted in order to quantify the uncertainty around the ICER, yielding information about the joint distribution of cost and effect differences. The bootstrapped cost-effectiveness ratios will be subsequently plotted in a cost-effectiveness plane, in which the vertical line reflects the difference in costs and the horizontal line reflects the difference in effectiveness. The choice of treatment depends on the maximum amount of money that society is prepared to pay for a gain in effectiveness, which is called the ceiling ratio. Therefore, the bootstrapped ICERs will also be depicted in a cost-effectiveness acceptability curve showing the probability that case management is cost-effective using a range of ceiling ratios.
Other study parameters
Demographic and injury-related characteristics will be analysed descriptively.
Interim analyses {21b}
Not applicable.
Methods for additional analyses (e.g. subgroup analyses) {20b}
Subgroups will be formed based on type of injury (stroke vs. other types) and severity, for which length of hospital stay will be used as a proxy (based on the distribution of the sample). Even though the subgroups are likely to be too small to draw firm conclusions, we will analyse this exploratively because the usual care for stroke is already better organized than for other types of brain injury (possibly lowering the additional gains of case management over care as usual for stroke compared to other types of brain injury) and because those with moderate to severe ABI may have more to gain from case management than those with mild ABI.
Methods in analysis to handle protocol non-adherence and any statistical methods to handle missing data {20c}
Data will be analysed by the intention-to-treat approach. A missing value analysis will be performed to determine the amount and kind of missing data and to detect patterns (i.e. missing at random or not). In case data is missing at random, imputation of missing data is not necessary because we will use a multilevel design.
Plans to give access to the full protocol, participant level-data and statistical code {31c}
The full protocol, anonymized data set and statistical code will be available on request after the results of the study have been published.
Oversight and monitoring
Composition of the coordinating centre and trial steering committee {5d}
Principal (CMvH), coordinating investigators (APMS; CR interim)
- Design of the study;
- Preparation of protocol and revisions;
- Ethics committee application;
- Study planning;
- Recruiting, training and supervising research assistants;
- Responsible for trial master file;
- Provide annual reports to ethics committee;
- Data verification;
- Publication of study reports;
Project team
(Principal (CvH) and coordinating (APMS; CR interim) investigators, overall project leader (JZ), intervention project leader (NJ), ReMinder monitoring tool project leader (KJ, MD)
- Agreement of final protocol;
- Recruiting hospital staff and assistance with recruiting procedures
- Implementing ReMinder;
- Entering participants in case management group into monitoring tool;
- Recruitment, training and supervising case managers;
- Collecting registrations of case management activities;
- Organizing project team meetings.
Composition of the data monitoring committee, its role and reporting structure {21a}
Because of the low burden and minimal risks no data monitoring committee was appointed.
Adverse event reporting and harms {22}
We will only report those adverse events that are directly related to our study, defined as experiencing negative consequences of case management in terms of psychosocial well-being or self-management, that are reported spontaneously by the subject. Due to the non-invasive nature of this study no experiment-related (serious) adverse events are expected.
Frequency and plans for auditing trial conduct {23}
As this study falls under the scope of the Dutch Medical Research Involving Human Subjects Act (Dutch: wet medisch-wetenschappelijk onderzoek met mensen, WMO), the Clinical Trial Centre Maastricht (Maastricht University) appointed an independent clinical research monitor to the study. This person monitors whether the study is conducted according to ICH-GCP guidelines and legislation and regulations. For our study, four visits divided over the study period are planned.
Activities of the clinical trial monitor are:
- Giving advice regarding laws and regulations;
- General control of data collection;
- Verification of source documents and CRFs;
- Controlling the compliance of laws and regulations;
- Complying all protocols;
- Checking of informed consents;
- Controlling the Trial Master File;
- Verifying the reports on adverse events and complications.
Plans for communicating important protocol amendments to relevant parties (e.g. trial participants, ethical committees) {25}
All changes (substantial and non-substantial) made to the study protocol after the favourable opinion was given by the accredited medical ethics committee (Medical Ethics Committee of Maastricht University Medical Center+) will be notified to the medical ethics committee, documented in the trial registration and communicated in the publication of the results of this study.
Dissemination plans {31a}
The results, whether positive or negative, will be disclosed unreservedly and submitted for publication to peer-reviewed scientific journals and presented on national and international conferences and meetings for healthcare professionals and people with ABI.