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. 2026 Aug 27;6:28. Originally published 2023 May 3. [Version 3] doi: 10.12688/hrbopenres.13700.3

Pilot of a person-centred, interdisciplinary approach to goal setting in Ireland’s National Rehabilitation Hospital: a study protocol

Lauren Christophers 1,2,a, Zsofia Torok 1,2, Catherine Cornall 2, Aine Carroll 1,2
PMCID: PMC13562921  PMID: 42732095

Version Changes

Revised. Amendments from Version 2

This version has been revised in response to a further peer review report. We have expanded methodological detail in several areas, including naming the quantitative measures in the Abstract, clarifying the patient and staff interview domains, and providing additional information on recruitment, informed consent, accessibility and supported participation. We have also clarified the role of the embedded researchers and strengthened the description of reflexivity within the qualitative component. The wording relating to documentation of protocol changes has been revised for clarity, and additional signposting has been added within the Methods to improve navigability. The patient and staff semi-structured interview guides are now provided as supplementary material. Minor editorial and consistency corrections have also been made throughout. These revisions clarify the prospectively developed study protocol and do not alter its underlying research questions or overall mixed-methods design.

Abstract

Background

Research has emphasised the value of a person-centred, interdisciplinary team (IDT) approach to structured goal setting in rehabilitation; yet these approaches are not consistently implemented in clinical practice, limiting the effect that goal setting can have on rehabilitation. The introduction of a new IDT, person-centred goal-setting process to Ireland’s National Rehabilitation Hospital (NRH) offers an opportunity to gain insight into barriers to implementing and normalising IDT goal setting in complex, specialist rehabilitation services. This process was developed prior to, and independently of, the current evaluation by the hospital’s quality improvement (QI) team; this protocol concerns the evaluation of its pilot implementation.

Method

The study was co-designed by embedded academic researchers and knowledge stakeholders, including the QI team responsible for introducing the new process and two former patients. A mixed-methods approach will capture patient and staff experiences and perspectives of the new process and, secondarily, pilot the feasibility of quantitative outcome measures ahead of a possible future hospital-wide evaluation. Data will be collected by embedded researchers using self-report measures and qualitative interviews with staff and patients. Measures include the Client-Centredness of Goal Setting scale (C-COGS), CollaboRATE, the Interprofessional Socialization and Valuing Scale (ISVS-9B), and the Normalization Measure Development questionnaire (NoMAD), capturing person-centredness of goals, shared decision-making, interprofessional socialisation and process normalisation. Quantitative data will be analysed using descriptive and, where appropriate, inferential statistics; qualitative interview data will be analysed using reflexive thematic analysis.

Discussion & Conclusion

The study aims to provide a holistic view of patient and staff experiences of the goal-setting process and to identify challenges and potential solutions to implementation within this context. Findings will inform further implementation within the hospital and contribute to rehabilitation practice around implementing IDT goal setting, adding an Irish perspective to the existing rehabilitation goal-setting literature.

Keywords: goal setting, person-centered care, interdisciplinary teams, rehabilitation, shared decision-making, interprofessional collaboration

Introduction

Rehabilitation is delivered by multi professional expert teams, focused on delivering interventions designed to optimize functioning and reduce disability in individuals with health conditions in interaction with their environment ( WHO, 2023). With these holistic and multidimensional aims, rehabilitation care is delivered by many different professionals who work together with varying levels of integration and collaboration. Where a multidisciplinary team (MDT) involves different disciplines working together with team members responsibilities focused on their own disciplinary remit, each discipline typically setting and pursuing its own goals with limited shared planning, an interdisciplinary team (IDT) involves more blurring of disciplinary boundaries ( Ellis & Sevdalis, 2019; Karol, 2014). An IDT includes members coming together, developing joint service plans and integrating closer to complete shared goals ( Ellis & Sevdalis, 2019). In the context of rehabilitation, goals are purposefully created and refer to a desired future state to be achieved by a person with a disability using rehabilitation activities and interventions ( Levack et al., 2015).

Thus, an IDT approach to goal setting is focused on creating shared goals across disciplines and has been advocated for as multiple goals set by different disciplines with patients can create confusion and miscommunication among patients and team members. Evidence based consensus statements recommend an IDT approach including goal setting for rehabilitation following traumatic brain injury for better outcomes ( Grabljevec et al., 2018; Miller et al., 2010). A critical review comparing factors impacting functional outcome for stroke found interdisciplinary models enhanced outcomes comparative to MDT models ( Cifu & Stewart, 1999). However, the vast majority of goal setting in rehabilitation care is multidisciplinary in nature as demonstrated in surveys, reviews and ethnographic observations across the UK and Australian rehabilitation services ( Baker et al., 2022a; Scobbie et al., 2015). How exactly an IDT can best work together to create common goals is unknown.

A shift from MDTs to IDTs also represents a shift from being discipline-oriented to being person focused ( Karol, 2014). For goal setting this is another important factor, the degree of “person centeredness” of the goals. Person centered care is focused on meaningful outcomes for an individual based on their life and their preferences ( Håkansson Eklund et al., 2019) and is underpinned by values of mutual respect, individual right to determination and compassion ( McCormack et al., 2010; McCormack & McCance, 2016). In rehabilitation, this perspective is particularly important because goals that reflect what the person considers meaningful in their own life can orient rehabilitation towards participation and outcomes that matter to them, rather than towards professionally determined impairments or activities alone. Although a person-centered approach to goal setting takes time and effort, it has been identified as worthwhile as centering practice around a person’s goal can provide clear structure for rehabilitation efforts, increase patient motivation and IDT communication, enhance patient engagement and is associated with goal attainment ( Doig et al., 2009; Ownsworth et al., 2008; Turner-Stokes et al., 2015). A person-centered approach that involves the patient in decisions about their goals is a process of shared decision making between the patient and the team members. Patients often report preferring a shared decision-making approach, though they can feel ill equipped or under prepared to do so, particularly at the start of the inpatient rehabilitation journey ( Baker et al., 2022a; D’Cruz et al., 2016; Rose et al., 2017; Rose et al., 2019). It is important that patients are equipped with relevant information both early on and throughout the goal setting process, which often does not occur ( Scobbie et al., 2015).

Thus, a best practice approach to goal setting is one that involves shared decision making with the patient, creating person centered goals to be shared by the rest of the team. Though there is evidence to indicate that patients who are more involved in the goal setting process experience greater improvements in their function ( Dalton et al., 2012; Turner-Stokes et al., 2015), shared decision making with the person during goal setting has been limited in clinical practice. Clinicians do not consistently use shared decision making in goal setting ( Cameron et al., 2018; Rose et al., 2017). Another reported patient preference is a structured approach to goal setting. For example, the commonly cited Goal setting and Action Planning (G-AP) framework incorporates useful strategies for enhancing goal setting such as action and coping planning, and goal review and feedback ( Scobbie et al., 2011). These strategies are also inconsistently implemented in practice, with a common absence of review and feedback in inpatient rehabilitation ( Plant & Tyson, 2018) and only 60% of UK community rehabilitation services reporting breaking down goals to action plans ( Scobbie et al., 2015).

There are clearly challenges to implementing and normalising best practices around goal setting. While the need for training and education for staff and patients has been highlighted ( Rose et al., 2017), the challenges of implementing and normalizing a collaborative, person centered, shared decision-making goal setting approach in rehabilitation are manifold. It is clearly difficult to introduce major changes to teamwork where most rehabilitation professionals work in a multidisciplinary rather than interdisciplinary way, where shared decision making requires time and additional supports for the patient and when rehabilitation teams are also adhering to organizational constraints and guidelines. Implementing goal setting interventions is a complex endeavor. Healthcare systems are characterized by being complex and adaptive, with different interacting agents at different levels influencing any change ( Carroll, 2021; Peters, 2014). Thus, research must focus on gaining insight into factors that can enable organizations and individuals to successfully implement changes in goal setting processes in line with what the literature has so far identified as best practice.

To this end, some researchers have explored implementation of strategies to support goal setting and how best to introduce and maintain a collaborative, shared decision-making approach. Scobbie et al. (2020) examined implementation of the G-AP framework in three community rehabilitation teams identified barriers such as an organizational set up that did not facilitate the process, lack of leadership support and team engagement and negative staff appraisal of the impact of practice change. Van de Weyer et al. (2010) explored perspectives around a keyworker led goal setting practice involving increased patient involvement and shared decision making. They reported barriers such as time needed to facilitate new practice, staff work patterns and staff level of skill. Doig et al. (2023) conducted qualitative interviews with professionals who trialed a role based, interdisciplinary goal setting process in inpatient rehabilitation for individuals with traumatic brain injury. Staff reflections emphasized the importance of putting the person at the centre, accepting the mind shift to participation focused goals and working collaboratively. The central challenge was described as the challenge of unlearning discipline specific goal setting ( Doig et al., 2023). Baker, Cornwell, Gustafsson, Stewart, et al. (2022b) used a co-design approach to implementing IDT goal setting and through focus groups identified barriers relating to clinicians lacking knowledge and understanding around goal setting terminology and processes. Following this, co-designed interventions for behavioral change included staff training modules, client held workbook and interdisciplinary goal conference templates and educational rehabilitation service fliers.

These studies have largely been conducted in the UK or Australia and have focused on specific diagnostic populations or on community rehabilitation. The generalizability of these findings to an Irish context is uncertain. It is likely that the implementation of complex interventions such as IDT goal setting requires tailoring to local context ( Baker et al., 2022b; Craig et al., 2013). Existing frameworks such as G-AP ( Scobbie et al., 2020), the keyworker-led model ( Van De Weyer et al., 2010), and role-based IDT goal setting ( Doig et al., 2023) were each developed for single-diagnosis or community rehabilitation populations. The NRH is Ireland’s only complex specialist rehabilitation hospital, serving a mixed diagnostic inpatient case-mix across acquired brain injury, stroke, spinal cord injury, limb absence, and paediatric programmes, within an existing structure that already includes formal family meetings. Rather than adopt a single-diagnosis framework unmodified, the hospital’s quality improvement team chose to adapt core best-practice principles identified in this literature; structured goal capture, action planning, regular review, and shared decision-making, into a process tailored to this mixed case-mix and to the hospital’s existing structures (see Intervention, below). The current study will add new perspectives to the literature by focusing on experiences of IDT goal setting from both staff and patients, in the context of an in-patient case-mix service in Ireland. From this, new insight may be gained into factors that can enable organizations and teams to successfully implement changes in goal setting and team working.

To summarise, best practices in goal setting in rehabilitation have been identified, but translating this into clinical practice has proven challenging. Given these obstacles, it is imperative that research continue to explore and identify solutions to the obstacles for successful implementation and normalization. In line with this, the outlined study will focus on the introduction of a tailored shared decision-making, interdisciplinary goal setting process in a mixed diagnostic case, inpatient rehabilitation setting – Ireland’s National Rehabilitation Hospital (NRH). To be explicit about the scope of this protocol: this study evaluates the pilot implementation of a goal-setting process that was co-designed and finalised prior to this evaluation; it is not a study of the development of that process, nor a naturalistic study of pre-existing, unstructured goal-setting practice. The constructs under evaluation, and how each is assessed, are summarised in Table 1 below.

Table 1. Constructs evaluated in this study and corresponding methods.

Construct Definition used in this study How it is evaluated
Interdisciplinary teamwork Team members work jointly across disciplinary boundaries toward shared goals (see Introduction for MDT/IDT distinction) Staff interviews (qualitative); ISVS-9B (interprofessional socialisation, quantitative)
Shared decision-making Patient and team jointly determine goals and priorities Patient interviews (qualitative); CollaboRATE (quantitative)
Person-centredness Goals reflect the individual’s own priorities, values and life context Patient interviews (qualitative); C-COGS (quantitative)
Goal setting The structured process of identifying, documenting and reviewing rehabilitation goals Staff and patient interviews; process documentation reviewed as part of the intervention description
Implementation/normalisation The extent to which the new process becomes embedded in routine practice Staff interviews (qualitative); NoMAD (quantitative)

Research questions, aims and objectives

Research Question 1: What is the patient experience and perspective of a shared decision making, interdisciplinary goal setting process in a rehabilitation hospital?

Research Question 2: What is the staff experience and perspective of a shared decision making, interdisciplinary goal setting process in a rehabilitation hospital?

Guided by these research questions, we intend to capture the patient experience of the new process, explore the degree of person centeredness of patients’ goals and whether the patient feels included in decisions about their care. From a staff perspective we will qualitatively explore their experience of the new process as well as how the process relates to their interprofessional values and socialisation. The quantitative measures address these same research questions from a complementary angle: rather than seeking new research questions of their own, C-COGS and CollaboRATE provide a standardised, repeatable measure of person-centredness and shared decision-making for Research Question 1, and the ISVS-9B and NoMAD provide standardised, repeated measures of interprofessional socialisation and normalisation for Research Question 2. This allows patterns identified qualitatively to be considered alongside a numeric, comparable account of the same constructs (see Study design and Data analysis, below).

Research Question 3: What are the barriers and enablers to implementing and normalising this process in a rehabilitation hospital?

Guided by this research question, we will use the data collected to identify barriers and enablers to implementation of an IDT goal setting process. These barriers and enablers can later be used to co-design behavioural interventions and further supports to facilitate hospital wide implementation of the goal setting process. This will likely be the subject of a later study by the project team.

Data will be collected by two embedded researchers. Embedded researchers have been defined as knowledgeable researchers working with a team that will be responsible for implementing changes ( Churruca et al., 2019). During the piloting of a shared decision-making IDT goal setting process within Ireland’s NRH, embedded researchers (LC and ZT) will a) capture staff and patient experiences of this new process, and b) identify potential barriers and enablers to implementation within the hospital, including responsibility for recruitment and eligibility screening of participants (see Eligibility criteria, below). Learning from this will not only be disseminated into the literature base, but feedback will be utilised by the quality improvement team within the hospital who are responsible for finalising and implementing a new goal setting procedure (see “Public and patient involvement”).

Methods

Study design

This study will use a mixed methods approach and is focused on the piloting of a shared decision making, interdisciplinary goal setting process with three teams in Ireland’s NRH. By capturing staff and patient experiences using multiple and mixed methods, we can gain insight into the phenomenon of shared decision making, IDT goal setting from different perspectives as well as barriers to implementation in this context. Qualitative and quantitative data will be collected from consenting staff and patients involved in the pilot, using semi structured interviews and self-report measures. The two strands serve complementary but distinct purposes. The qualitative interviews are designed to answer Research Questions 1–3 directly, eliciting patient and staff experience of the process in depth. The interview domains and data collection procedures are described below under Qualitative data, with the analytic approach described under Data analysis. The quantitative self-report measures serve two secondary purposes: first, to provide a standardised, repeatable measure of staff interprofessional socialisation (ISVS-9B) and process normalisation (NoMAD), and of patient-perceived client-centredness (C-COGS) and shared decision-making (CollaboRATE), which can be compared descriptively across time points and considered alongside the qualitative account; and second, to pilot the feasibility and acceptability of these instruments, developed and validated in Australian and North American settings, for possible use in a future, hospital-wide evaluation of the goal setting process. Given the small anticipated sample, the quantitative strand is treated as descriptive and exploratory rather than as a primary hypothesis test. This is a convergent mixed-methods design: quantitative and qualitative data will be analysed separately and then integrated at the interpretation stage (see Data analysis). It should be noted that elements of this study design may be subject to change due to organisational constraints and factors beyond the researcher’s control. Any substantive changes to the study design will be documented in subsequent versions of this protocol and reported transparently in publications arising from the study.

Study setting

This study will take place in the NRH, Ireland, a 120 bedded rehabilitation hospital. The NRH is a national, specialist, tertiary university hospital providing complex specialist rehabilitation services to adults and children who have an acquired illness or injury. The NRH is a part of the Ireland East Hospital Group and Ireland’s Integrated Rehabilitation pathway with close clinical links with national spinal and neurosurgical centres at acute hospitals. As Ireland’s only complex specialist rehabilitation hospital the NRH accepts patients from hospitals and health care facilities throughout the country. Consultant led interdisciplinary teams provide speciality programmes in acquired brain injury; stroke; spinal cord system of care (SCSC); prosthetic, orthotic and limb absence rehabilitation (POLAR), and paediatric family-centered rehabilitation. The Stroke, POLAR and paediatric programmes each have one in-patient unit, SCSC programme has three units, and the Brain Injury programme has four units. The hospital is transitioning from paper healthcare records to an electronic patient record system (EPR). The new goal process designed for an EPR is being introduced initially in paper format.

Eligibility criteria

The study will recruit participants among the patients and staff of the NRH. A convenience sampling approach will be used: all eligible staff on the three participating units, and all eligible patients admitted to those units during the recruitment window, will be invited to participate. Recruitment and determination of eligibility will be carried out by the two embedded researchers (LC and ZT), in liaison with each unit’s clinical lead.

Eligible patient participants will be the inpatients receiving rehabilitation in the NRH, admitted to one of the units enrolled in the intervention study, after the introduction of the new goal setting process. Where a patient has a cognitive or communication impairment, the treating team will first consider whether existing, hospital-approved communication supports (for example communication passports, augmentative and alternative communication aids already in use for that patient, or a family/carer-supported interview) can enable safe and meaningful participation. Patients will be excluded only where these supports are judged clinically insufficient to gain valid consent and to elicit the patient’s own view.. Staff members eligible for study participation are members of the interdisciplinary team on a participating unit directly involved in the goal setting process, including medical, nursing, and health and social care professional (HSCP) staff (for example physiotherapy, occupational therapy, speech and language therapy, social work and psychology) and healthcare assistants, working on that unit during the time of the trial. Administrative and non-clinical staff are not included.

Recruitment and consent

Potential patient participants will receive written information about the study from the clinical team. Those willing to be approached will then meet with a researcher, who will explain the study, provide an opportunity to ask questions and allow time for consideration before written informed consent is obtained. Participation is voluntary and will not affect clinical care. Where a participant is unable to sign, consent will be documented in accordance with the approved study procedure.

For staff participants, study information will be provided before consent is sought, with participation voluntary and unrelated to employment or professional relationships within the hospital.

Particular attention will be given to accessibility and supported participation for patients with cognitive or communication impairments. As outlined in the eligibility criteria, existing hospital-approved communication supports may be used to facilitate understanding, communication and expression of the patient’s own views. Eligibility will therefore not be determined solely by the presence of a cognitive or communication impairment; exclusion will occur only where available supports are insufficient to enable valid consent and meaningful participation.

Intervention

This study will focus on the pilot of a new goal setting process in Ireland’s NRH. This process was developed prior to, and independently of, this evaluation study, by the NRH’s IDT Quality Care Team. The new goal process was developed in response to feedback from and in collaboration with NRH staff and patient representatives. Development took place over a two-month co-design period involving weekly workshops with a wider co-design group comprising three academic researchers (including the two embedded researchers responsible for this evaluation, LC and ZT), two former patients, and staff representatives from medicine, nursing and HSCP disciplines (see Public and Patient Involvement). In the implementation of complex healthcare interventions, it is likely that a co-design approach with tailoring to specific contextual barriers and enablers will be more successful ( Craig et al., 2013). The new goal process was created with this in mind, informed by iterative rounds of feedback from staff and patients. As set out in the Introduction, existing goal-setting frameworks reported in the literature (e.g., Scobbie et al., 2020; Van De Weyer et al., 2010; Doig et al., 2023) were developed for single-diagnosis or community rehabilitation populations; the co-design group instead adapted core best-practice principles from this literature into a process tailored to the NRH’s mixed diagnostic case-mix and its existing structures, including its established family meeting model. It spans the rehabilitation journey from pre-admission to the NRH inpatient rehabilitation programmes to discharge and life after the NRH. Documentation to capture goals and the interdisciplinary care plan was changed to meet the requirements of the introduction of the EPR.

The change of the goal setting process is being accomplished in an iterative manner, based on the principles of person-centredness, partnership and patient goals driving the rehabilitation activities and schedule. Prior to admission, the goal process will be introduced to the patient and/or family through contact with members of NRH staff providing both written (a single information booklet used across all specialties, with a short specialty-specific insert) and verbal information. Gathering the person and family’s story—in order to get to know the person and what matters most to them—will capture the patient’s or their representative’s understanding of their health condition, hopes and visions for life after rehabilitation and their three to five identified goals for their admission, including their perception of the importance of each goal and their proximity to achieving it. Where a patient is unable or does not wish to lead their own goal-setting, a named key worker (typically from nursing or allied health) leads goal capture collaboratively with the patient and family, adjusting the level of support to the patient’s stated preference and capacity. Recognised tools and accessible supports used at the ‘meet the team’ session include the hospital’s existing communication aids, for example Talking Mats, easy-read materials, and interpreter services where required.

The initial goals will be discussed during a goal capturing meeting held within the first two–five days of admission. As soon as practical within the first two weeks, the goal, action and care planning meeting (the goal-setting conference) will take place, where the patient and/or family will meet with key members of the interdisciplinary team (medical, nursing; HCA and relevant HSCP staff ) to formally document the patient’s long-term goals in the EPR. The team, together with the patient and/or family then collaborate on identifying the short-term goals that underpin each longer-term goal identified. The new documentation captures the patients’ identified goals; the short-term goals underpinning the main goals; tasks and actions to be completed by both IDT members and the patient and factors that will support or interfere with achievement. Establishing peer patient group sessions to discuss long and short-term goals will be introduced and will take place on a regular basis.

Reviewing and revisiting goals will be a continuous process that is both formal and informal and includes the person and/or their family. New short-term goals can be added at any time and the patient may also revise their long-term goals during any of their goal review meetings and discussion. The interdisciplinary team review on a weekly basis may also include longer sessions with the patient and family, incorporating the patient’s and/or family’s own feedback on progress towards goal outcomes and can be complemented by intermittent formal IDT review meetings with the patient and/or family ( Figure 1).

Figure 1. The new IDT goal setting process.


Figure 1.

Staff training accompanied the roll-out of the new process on each unit. This comprised system-wide briefing sessions delivered by the IDT Quality Care Team prior to go-live on each unit, covering the rationale for the new process, the revised documentation, and worked examples of person-centred goal capture. Unit-based staff champions were identified on each participating unit to provide ongoing peer support during the pilot period.

A structured description of the intervention, mapped against the TIDieR checklist ( Hoffmann et al., 2014), is provided in Table 2.

Table 2. TIDieR description of the goal-setting process intervention.

Item Description
Brief name New interdisciplinary, person-centred goal setting process
Why To replace discipline-siloed goal setting with a shared, person-centred, interdisciplinary process spanning admission to discharge (see Introduction)
What (materials) Pre-admission information booklet (with specialty-specific insert); revised EPR/paper documentation for long- and short-term goals, tasks and actions; communication aids (e.g., Talking Mats, easy-read materials)
What (procedures) Pre-admission contact; ‘meet the team’ session; goal capturing meeting (days 2–5); goal, action and care planning meeting/goal-setting conference (within 2 weeks); weekly IDT review; family meetings; peer patient group sessions; pre-discharge meeting
Who provided Interdisciplinary team members (medical, nursing, HCA and relevant HSCP staff ), with a named key worker where a patient requires additional support to lead their own goal-setting
How Face-to-face, individually and collectively (team conferences, family meetings)
Where Three inpatient units of the National Rehabilitation Hospital
When and how much Spans pre-admission to discharge and follow-up; goal-setting conference within 2 weeks of admission; weekly review thereafter
Tailoring Adapted from existing goal-setting frameworks in the literature to the NRH’s mixed diagnostic case-mix and existing family meeting structure (see Introduction, Intervention)
Modifications Any changes made during the pilot will be logged and reported in the results paper

Data collection

Quantitative data

Measures

For patients the self-report measures (C-Cogs and CollaboRATE) will be administered shortly after the goal, action and care planning meeting (the goal-setting conference described above, occurring within the first two weeks of admission; distinct from the earlier ‘meet the team’ session) (see intervention description). These measures are designed for use after a specific consultation and are therefore best used in this way. For patients who wish to complete these measures but face literacy, fatigue or motor barriers to doing so unaided, researchers (LC/ZT) are available to read items aloud, clarify wording, or transcribe responses. For staff participants the ISVS-9B will be administered at three time points (prior to the trial, after new goal setting process has begun, and at the conclusion of the trial) and the NoMAD administered alongside it at time three. See Table 3 above for data collection time points.

Table 3. Data collection timeline.

Time 1: before trial Time 2: after initial goal setting meeting Time 3: after trial
Staff measures ISVS-9B ISVS-9B Semi structured interview; ISVS-9B; NoMAD
Patient measures N/A C-Cogs and CollabORATE Semi structured interview

Patient measures

C-Cogs

The Client-Centredness of Goal Setting (C-COGS) ( Doig et al., 2015) is a 13 item instrument designed to measure the degree of client-centredness of goal-planning approaches from the client’s perspective. It has three subscales (Alignment, Participation and Goals) and is scored on a 5-point Likert scale (1 = Strongly disagree, 5 = Strongly agree). The participation sub-scale measures the person’s perceived participation in the goal setting process and can be scored separately (range 6–30). The goals sub-scale measures the ownership, importance, meaningfulness and relevance of the individual rehabilitation goals, and the average is calculated across the goals (range 4–20). A total score can be generated by adding the sub-scale scores, higher total C-COGS scores indicating higher levels of client-centredness of goal planning. The C-COGS is characterised by good internal consistence (Cronbach alpha = 0.82) ( Prescott et al., 2019).

CollaboRATE

The CollaboRATE ( Barr et al., 2014) is a short patient-reported measure of shared decision making that patients complete following the goal planning meeting. It contains three brief questions, measuring the dimensions of the health issue, the elicitation, and the integration of patient preferences. It is rated on 5-point Likert scale (0 = No effort was made, 4 = Every effort was made), scores ranging from 0–12. Higher scores indicate greater efforts made to support the patient’s participation in the shared decision-making process. The CollaboRATE evidences concurrent validity with other measures of shared decision-making and excellent intra-rater reliability ( Barr et al., 2014).

Staff measures

ISVS-9B

The ISVS-9B is the short version of the original 21 item Interprofessional Socialization and Valuing Scale (ISVS-21) ( King et al., 2016). It is a self-report instrument, assessing individuals’ beliefs, behaviours, and attitudes and is designed to measure interprofessional socialization and readiness to function in interprofessional teams. The three subscales reflect three key concepts of interprofessional practice: roles (belief ), client-centeredness (attitudinal items), and conflict/negotiation (behavioural items). The scale was developed to evaluate the effect of interprofessional education and other interventions, in a pre-post-test study design. It is rated on 7-point Likert scale (7 = To a Very Great Extent, 1 = Not at All) and contains the option of choosing the “N/A” (not applicable). The scores are ranging from 0–63, higher scores indicating more positive views and higher expression of interprofessional socialization behaviours. The ISVS-21 is characterised with an excellent internal consistency (Cronbach alpha = 0.98).

NoMAD

The Normalization Measurement Development questionnaire (NoMAD) ( Finch et al., 2018) is a 23-item instrument, measuring the normalisation of complex healthcare interventions. It is based on normalisation process theory (NPT) and was developed for evaluating the status or outcome of an implementation process and the sustainability of the intervention. The first part contains three general questions about the intervention, the second consists of 20 items reflecting the four NPT constructs (coherence, cognitive participation, collective action and reflexive monitoring). The questions in the second part have two categories of answers: Option A has five options (strongly disagree–strongly agree), while the Option B participants can choose if the statement is not relevant. While the NoMAD does not have a defined scoring guide, it is often scored on a five-point Likert scale (1 = strongly disagree, 5 = strongly agree) ( Gillespie et al., 2018; Lamarche et al., 2022). The NoMAD is characterised with good psychometric properties, demonstrating sufficiently high levels of internal consistency along the four dimensions (Cronbach alpha = 0.89).

Qualitative data

Qualitative data will be collected from participating patients at the conclusion of the pilot using semi-structured interviews. A flexible topic guide will support participants to describe their experience of the goal-setting process while retaining autonomy over the direction and emphasis of the discussion. Open-ended questions will explore goal setting, participation in decision-making, relationships with the rehabilitation team, information and communication, and perceived facilitators and challenges across the rehabilitation admission. The topic guide was developed by the embedded researchers, reviewed by the co-design team and specifically reviewed and refined with the two former patients involved in the co-design process. Qualitative data will also be generated through semi-structured interviews with participating staff. Open-ended and reflective questions will address interdisciplinary teamwork and interprofessional collaboration, person-centered care, shared decision-making, experiences of the new goal-setting process, and perceived barriers and enablers to its implementation and normalisation. The topic guide was developed by the researchers, reviewed by the co-design team and specifically reviewed and refined by staff representatives from different disciplines. The embedded researchers conducting interviews will not be members of participants’ treating teams. Given their embedded role within the implementation team, reflexive attention will be paid to how prior relationships, organisational knowledge and researcher assumptions may influence data generation and interpretation. Common semi-structured topic guides and agreed study procedures will support consistency across interviews while retaining the flexibility appropriate to qualitative interviewing.

Data management

All collected data will be safely stored and used in accordance with the Data Protection (Amendment) Act of 2003 and General Data Protection Regulation (GDPR) 2016/679. Participants’ data will be de-identified and will be presented in reports and publications either in aggregate form or, where necessary, using pseudonyms.

Data analysis

Quantitative data

Data from self-report measures will be imported into SPSS (IBM SPSS Version 27; an open access alternative is R, or R Studio). Descriptive statistics will be used to illuminate the means, standard deviations etc., of the patient measures – C-Cogs and its subscales as well the 3-item collaboRATE. Given the small sample of patients undergoing the trial, more comprehensive or inferential statistics are not appropriate (Maximum potential sample size of 16 patients). However, these measures can be used complementary to qualitative data to gain insight into the patient experience of the new goal setting process. Furthermore, the study offers the opportunity to pilot these measures with a view to potentially using them in a hospital wide impact study in the future.

For the staff self-report measures, inferential statistics can be used to test the following hypothesis:

H1a: Interprofessional socialisation and values scores will significantly change over the course of the trial.

A one-way repeated measures analysis of variance (or suitable non-parametric alternative) can be used to test whether scores significantly change over time. An a priori power analysis was conducted using G Power and indicates that with an alpha level of 0.05, a sample of 27 staff members would be required to achieve 80% power in detecting a medium effect size. Descriptive statistics will be calculated for the staff NoMAD data – in order to investigate the perspective of staff on normalisation and implementation of this new goal setting process across the hospital.

Mixed-methods integration

This is a convergent mixed-methods design. Quantitative and qualitative data will be analysed separately using the methods described above, and integrated at the interpretation stage through a narrative weaving approach, using the qualitative findings to help explain and contextualise the quantitative results (for example, using interview data to interpret patterns observed in NoMAD subscale scores), rather than a fully joint-display integrated analysis, which was judged disproportionate given the modest quantitative sample size.

Qualitative data

Theoretical grounding

The researchers will take a constructionist perspective, with a critical orientation to the analysis of qualitative data. Based on this we have selected reflexive thematic analysis as the primary method of analysis. We recognise language as an implicit tool in socially producing meaning and understanding of experiences. In this view, participants in interviews are not merely sharing their experiences but rather reflecting upon memories and constructing meaning as topics are discussed. A critical orientation to analysis means that we understand firstly, the artificial and constructed nature of the interview but also that we aim to see beyond language. If language creates one’s subjective reality, then we aim to offer interpretations of meaning beyond those explicitly stated by the participants. In the language of reflexive thematic analysis – this means including latent codes alongside semantic ones, taking an inductive approach in conjunction to a deductive one and keeping a critical perspective rather than a more essentialist one.

Analysis method

Consistent with the constructionist theoretical orientation outlined above and the study research questions, qualitative interview data will be analysed using Braun and Clarke’s reflexive thematic analysis. The lead researcher (LC) will cycle through Braun and Clarke’s six phases in an iterative, exploratory approach (familiarisation with data, generating initial codes, generating themes, reviewing themes, defining and naming themes, reporting themes) ( Braun & Clarke, 2006, Braun & Clarke, 2021; Terry et al., 2017). Following transcription, the researcher will read and re-read transcripts while listening to audio recording, thus immersing herself in the data. The lead researcher (LC) will import the data to NVivo and will begin initial coding. A predominantly inductive approach will be taken with open coding on both patient and staff interview data. Codes will include semantic codes which summarise a data segment and latent codes which interrogate a deeper, underlying meaning behind a data segment. This will be based on the interpretation of the researcher. With the generation of a set of initial codes, similar meaning units will be clustered to create themes and sub-themes. From here we aim to use this analysis to construct an understanding of the patient and staff experience of the trial. For staff, this will include attitudes and expectations prior to the trial as well as reflections after the trial through using two interviews. For patients, the goal setting journey is elicited through reflections during one interview at the conclusion of the trial.

Ethics

Ethical approval for this study has been granted by the NRH Research Ethics Committee (date of approval 24/05/2022) and the UCD Office of Research Ethics (Research Ethics Exemption Reference Number LS-E-22-06-Carroll, date of approval 13/01/22).

Public and patient involvement

This study was co-designed by embedded academic researchers and knowledge stakeholders. The co-design team includes two former patients, members of the NRH’s IDT Quality Care Team who are responsible for organizing the implementation of new goal setting processes, and three academic researchers. The new goal setting process itself was designed by this co-design group prior to, and independently of, this evaluation study; the same group also collaboratively decided on the research questions, measures and methods for the evaluation described in this protocol. This study was rapidly co-designed over a two-month period. The co-design team met weekly and collaboratively decided on appropriate research questions, measures and methods outlined in this document.

The involvement of clinicians and former patients goes beyond stakeholder consultation, as the co-researchers are contributing not only clinical expertise and knowledge alone butactively co-designed the research study collaboratively making decisions on measure selection, interview questions etc.. There is evidence that involving patients not only brings lived-experience perspective into research but increases its quality and the relevance ( Brett et al., 2014; Nierse et al., 2012). Co-designing with healthcare professionals has been identified as a key factor in successful implementation of healthcare interventions and uptake of research findings ( Jessup et al., 2018). The co-design team will continue to be involved throughout the research process and thus encourage organisational uptake of research findings.

Dissemination of results

A bespoke dissemination plan will be developed. We will share the iterative process during the active phase of data gathering with the internal academic and clinical community. Upon completion we will share findings in public venues (library, hospital and university space), round table discussions (academic and clinical venues), and academic presentations and workshops both within and outside of the hospital community. The end users and stakeholders are the patient and carers, academic, clinical, and managerial staff who can take findings and initiate action to address the issues identified in the project. Academic and clinical educators can also utilize the project presentation to educate clinicians, students and goal setting. Results of this study will also be disseminated through publication in in peer-reviewed academic journals and on social media. Findings will be also presented at national and international conferences and to relevant stakeholder groups.

Study status

This study is in progress, in line with introduction of the new goal setting process within the hospital. The baseline (time 1) data collection for staff is currently underway.

Conclusions/Discussion

The value of a person-centered approach to goal setting in rehabilitation is clear – it can result in better functional outcomes and increased patient satisfaction. However, there have been issues in implementing new goal setting approaches to complex healthcare systems. Without investigating implementation of complex healthcare interventions, we run the risk of “shared decision making” or “interdisciplinary teams” or “person centered” becoming tokenistic phrases rather than real life practices. Indeed, research has identified that many rehabilitation teams describe themselves as interdisciplinary despite not meeting evidence-based criteria to qualify as one ( Baker et al., 2022a), shared decision making is something that clinicians can describe but do not always use these skills in practice ( Cameron et al., 2018); clinicians and teams do not consistently implement goal setting strategies into practice, limiting the effect that goal setting can have on rehabilitation ( Marsland & Bowman, 2010; Plant & Tyson, 2018; Scobbie et al., 2015). The introduction of an interdisciplinary, person-centered goal setting process to Ireland’s NRH offers an opportunity to gain novel insight into mixed case mix diagnosis rehabilitation services and the potential barriers to implementing and normalising such complex changes. Patient and staff experience and perspectives may further illuminate challenges and potential solutions to implementing changes to goal setting within this context. From this we hope to offer recommendations for rehabilitation practice around implementing changes to goal setting processes.

Limitations

One limitation is the data collection time frame, which is set by organisational factors. The goal setting process and new documentation is due to be finalised in tandem with the introduction of an electronic patient record system within the hospital. This places constraints on the time that can be spent on data collection, though the co-researchers and authors have worked together to ensure that activities are feasible. A second limitation is the study sample, which may not be a wholly representative sample of staff. There is a possibility of recruitment bias whereby only people interested in changes in goal setting will participate. We also acknowledge limited participation of staff working night shifts or less flexible time schedules. Despite efforts to support participation through existing communication aids (see Eligibility criteria), patients with the most severe cognitive or communication impairments will still be unable to participate, and our patient sample will therefore under-represent this group. A small sample of patients is expected as a small number of admissions are anticipated in the time available for recruitment. However, the sample will be appropriate to achieve qualitative data saturation ( Hennink & Kaiser, 2022) from interview data. Finally, a potential limitation of this study is the questionnaires used with staff and patients which were developed in Australia and USA, and therefore have not been validated or adapted for use within an Irish context. A further limitation is that the co-design group that developed both the goal setting process and this evaluation protocol included two former patients but no family carers, and both patients had experience of a single diagnostic pathway rather than the full range of conditions seen at the NRH (including acquired brain injury, stroke, spinal cord injury, limb absence and paediatric rehabilitation). This may mean that both the process and this study design reflect that experience more than others; future iterations of this work should aim to widen patient and carer representation across the hospital’s full case-mix.

Data availability

No data are associated with this article.

Acknowledgements

The authors must thank the other members of the co-design team - Clare Hudson, Teresa Whyte, Aoife Henn, Sacha Dekker and Declan Naughton. The sharing of their perspective as staff and former patients, greatly contributed to the study design.

Funding Statement

The current study is part of a larger project (INSPIRE-NRH) which is funded by the National Rehabilitation Hospital Foundation (NRH Foundation, Project Code R22626). This grant is assigned to principal investigator of the project, Prof Aine Carroll. The funders have had no influence in the development of the review question and methodological approach reported in this protocol.

The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

[version 3; peer review: 2 approved, 1 approved with reservations, 1 not approved]

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HRB Open Res. 2026 Sep 12. doi: 10.21956/hrbopenres.16025.r57562

Reviewer response for version 3

António Lista 1

Dear authors,

This protocol addresses a relevant question in rehabilitation: how to involve people in setting their own goals and organise teamwork around those goals. The research questions are clear, and the combination of interviews and questionnaires seems appropriate. The changes made in response to previous reviews have helped clarify the intervention and the procedures for participation in the study.

During my reading, a few questions remained that I would welcome the authors’ clarification on:

  1. In Table 3, staff interviews appear only at the end of the pilot. However, the qualitative analysis section refers to two interviews, before and after the pilot. Are one or two interviews planned? If two, will the same staff members be interviewed at both time points? It would also be useful to specify the recruitment duration and the intervals between assessments. For patients, does the interview take place at the end of their admission or at the end of the overall pilot?

  2. The quantitative component is described as exploratory, but a hypothesis and a sample size calculation are then presented to test changes over time. I do not see these choices as necessarily incompatible, but it would help to explain how they fit together and how the findings will be interpreted. Please also clarify which score will be analysed and how incomplete assessments and loss to follow-up will be handled. The description of NoMAD as a repeated measure should be revised, as it is scheduled for administration only at the end of the pilot.

  3. The authors state that they intend to assess the feasibility and acceptability of the questionnaires for a future study. How will this be done? Will they collect participant feedback, record difficulties with completion, or examine missing responses? A brief explanation would help readers understand how this objective will be addressed.

  4. The description of the goal-setting process is helpful, and the authors explain why it needed to be adapted to the hospital context. However, I would welcome a clearer explanation of how the cited frameworks informed the choices made. Which principles were used to develop the process, and how are these reflected in the person’s participation, the negotiation of goals, and the review of the plan?

Finally, the Study Status section seems to refer to an earlier stage than that described in the responses to reviewers. 

I suggest updating this statement. It would also be helpful to include a direct link to the interview guides mentioned as supplementary material.

I believe this study could make a useful contribution to rehabilitation practice. The clarifications above would help readers understand what is planned and resolve some inconsistencies between sections of the protocol.

Is the study design appropriate for the research question?

Yes

Is the rationale for, and objectives of, the study clearly described?

Yes

Are sufficient details of the methods provided to allow replication by others?

Partly

Are the datasets clearly presented in a useable and accessible format?

Not applicable

Reviewer Expertise:

Rehabilitation nursing; ageing; functional assessment; person-centred care; quantitative research methods and evidence synthesis.

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however I have significant reservations, as outlined above.

HRB Open Res. 2026 Sep 3. doi: 10.21956/hrbopenres.16025.r57543

Reviewer response for version 3

Yvonne Codd 1

No further comments to make.

Is the study design appropriate for the research question?

Yes

Is the rationale for, and objectives of, the study clearly described?

Yes

Are sufficient details of the methods provided to allow replication by others?

Partly

Are the datasets clearly presented in a useable and accessible format?

Partly

Reviewer Expertise:

My background and research experience are in enduring health conditions, service design, and rehabilitation research, including the design and evaluation of studies examining person-centred rehabilitation outcomes and clinical practice.

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

HRB Open Res. 2026 Aug 10. doi: 10.21956/hrbopenres.15995.r57016

Reviewer response for version 2

Yvonne Codd 1

Abstract:

Clear outline on the rationale for this work and a good account of the planned steps for the evaluation within this protocol. Further detail on the methods would strengthen this section - specifically - name the measures designed being used? what qualitative approaches will be used for interview analysis?

Introduction

The distinction between uni-disciplinary and interdisciplinary goal setting and the potential challenges of this is nicely laid out is paragraphs one and two, Paragraph three positions the patient as a shared decision-maker in the goals being set, however, I wonder would it be valuable to a sentence or two that more explicitly considers the patient's unique perspective on goals and priorities for rehabilitation and how this can influence patient engagement and perceptions of QoL?   - Inclusion of this would, I think align well with later points by Doig et al., (2023) about the need to shift towards participation-focused goals.

Methods

Some further development of the qual methods would strengthen this section - themes being explored within the questions and I would suggest inclusion of the semi-structured interview guide as part of the protocol. Development to include how the interview guides were pilot tested, any revisions made. Type of qualitative analysis planned should be considered.

It is unclear if the two embedded researchers will both complete both qual and quant aspects of data collection or if each are assigned to a single strand. Some development regarding planned steps to minimize bias, ensure a common approach to data collection with the interviews, and reflexivity would be useful within the data collection section.

"Any changes to the study design will be registered with the protocol." - Is the protocol registered elsewhere? - if so the registration number and site should be added to this paper.

Recruitment

Some further details required on disseminating the study information, voluntary informed consent (for both staff and patients), cooling off periods, steps to reduce perceptions of coercion given the researchers are embedded etc, also given some patients have a cognitive or communication impairment - how will this be navigated in the recruitment and data collection phases? - this point is later somewhat considered in the limitations sections, and I wonder would clearer inclusion criteria assist in clearer consideration of eligibility and decisions around this.

Overall Comments

This protocol addresses an interesting and clinically relevant study question, with the potential to directly inform rehabilitation practice. Overall, the study is well motivated, and the protocol provides a useful foundation for the proposed work.

Providing greater detail on some aspects of the planned methods and analysis would further strengthen the protocol and enhance clarity for the reader. As I progressed through the full manuscript, I noted that some of my initial queries were subsequently addressed in later sections. This made me wonder whether some resequencing of the manuscript, particularly within the Methods section, might improve the overall flow and ensure that key information is presented closer to where it is first required. Such restructuring may also help to address some of the questions that arose during my reading and make the protocol easier to follow.

Editing Considerations

Suggest editing review so that abbreviations (MDT)  (NRH) (IDT) are used consistently after full terms are first explained.

Is the study design appropriate for the research question?

Yes

Is the rationale for, and objectives of, the study clearly described?

Yes

Are sufficient details of the methods provided to allow replication by others?

Partly

Are the datasets clearly presented in a useable and accessible format?

Partly

Reviewer Expertise:

My background and research experience are in enduring health conditions, service design, and rehabilitation research, including the design and evaluation of studies examining person-centred rehabilitation outcomes and clinical practice.

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however I have significant reservations, as outlined above.

HRB Open Res. 2026 Aug 18.
Áine Carroll 1

Response to Reviewer

We thank the reviewer for the thoughtful and constructive review and for recognising the clinical relevance of the study, the clarity of its rationale and the appropriateness of the study design. We particularly appreciated the observation that some methodological information became apparent only later in the manuscript. In response, we have strengthened methodological signposting, provided additional detail on recruitment and consent, clarified the qualitative interview domains and the role of the embedded researchers, made reflexivity more explicit, and clarified the abstract. We have also reviewed the manuscript for consistency in the use of abbreviations.

Abstract

Reviewer comment:

The abstract provides a clear rationale and overview, but further methodological detail would strengthen it, particularly the names of the measures used and the qualitative analytic approach.

Response:

Thank you. We have revised the Methods section of the abstract to name the four quantitative measures used in the study: the Client-Centredness of Goal Setting scale (C-COGS), CollaboRATE, the Interprofessional Socialization and Valuing Scale (ISVS-9B), and the Normalization Measure Development questionnaire (NoMAD). We have also made explicit that qualitative interview data will be analysed using reflexive thematic analysis.

The revised abstract now states:

Self-report measures include the Client-Centredness of Goal Setting scale (C-COGS), CollaboRATE, the Interprofessional Socialization and Valuing Scale (ISVS-9B), and the Normalization Measure Development questionnaire (NoMAD), capturing person-centredness of goals, shared decision-making, interprofessional socialisation and process normalisation. Quantitative data will be analysed using descriptive and, where appropriate, inferential statistics; qualitative interview data will be analysed using reflexive thematic analysis.

The original abstract already identified the constructs and reflexive thematic analysis; the revision makes the instruments themselves explicit.

Introduction

Reviewer comment:

The reviewer suggested making the patient's unique perspective on rehabilitation goals and priorities more explicit, including how this may influence engagement and participation.

Response:

Thank you. We agree that the particular contribution of the patient's own priorities could be made more explicit. We have therefore added a sentence to the discussion of person-centred goal setting emphasising that meaningful rehabilitation goals should be oriented towards participation and outcomes that matter to the individual rather than being determined solely by professional priorities.

The following sentence has been added:

In rehabilitation, this perspective is particularly important because goals that reflect what the person considers meaningful in their own life can orient rehabilitation towards participation and outcomes that matter to them, rather than towards professionally determined impairments or activities alone.

We have retained the focus on meaningful goals, participation and engagement rather than introducing quality of life as a separate construct, as quality of life is not an outcome being evaluated in this protocol. The existing Introduction already links person-centred goals with motivation, engagement and goal attainment.

Methods: qualitative methods and interview guides

Reviewer comment:

The reviewer requested greater detail on the qualitative methods, including the topics explored in the interviews, development and testing of the interview guides, and the planned qualitative analysis. Inclusion of the semi-structured interview guides was also suggested.

Response:

Thank you. We have expanded the qualitative data collection section to describe more explicitly the areas explored in both patient and staff interviews.

For patients, the revised text clarifies that open-ended questions explore goal setting, participation in decision-making, relationships with the rehabilitation team, information and communication, and perceived facilitators and challenges across the rehabilitation admission.

For staff, the revised text clarifies that interviews address interdisciplinary teamwork and interprofessional collaboration, person-centred care, shared decision-making, experiences of the new goal-setting process, and perceived barriers and enablers to implementation and normalisation.

We have also clarified that the interview guides were developed by the researchers and reviewed and refined through the co-design process, including specific review by former patients and staff representatives. They were not subjected to a separate formal pilot test, and we have not retrospectively described this process as pilot testing.

The patient and staff semi-structured interview guides have also been included as supplementary material.

The existing manuscript already specifies the constructionist orientation, reflexive thematic analysis and Braun and Clarke's iterative analytic process; we have strengthened signposting to make this information easier to locate.

Methods: embedded researchers, consistency and reflexivity

Reviewer comment:

The reviewer asked for clarification regarding the roles of the two embedded researchers in qualitative and quantitative data collection, and for further detail on consistency of interviewing, potential bias and reflexivity.

Response:

Thank you. We have clarified the role of the embedded research team and added explicit consideration of reflexivity.

The revised manuscript states that the embedded researchers contribute to data collection across the study as required. Common study procedures and semi-structured topic guides support consistency in data collection while retaining the flexibility appropriate to qualitative interviewing.

We have also clarified that embedded researchers conducting patient interviews are not members of participants’ treating teams. Given their embedded position within the implementation team, we have added explicit consideration of how prior relationships, organisational knowledge and researcher assumptions may shape data generation and interpretation.

We have deliberately framed this issue in terms of reflexivity rather than attempting to suggest that researcher subjectivity can be eliminated, consistent with the constructionist orientation and reflexive thematic analysis adopted in the protocol.

The later conduct of the patient study confirms the distinction between researchers' embedded implementation role and the participants' treating teams, although the protocol itself retains the personnel and roles prospectively specified at the outset.

Methods: protocol registration

Reviewer comment:

The reviewer queried the statement that changes to the study design would be “registered with the protocol” and asked whether the protocol was registered elsewhere.

Response:

Thank you for identifying this ambiguity. The wording did not refer to a separate trial or protocol registration.

We have replaced the sentence with:

Any substantive changes to the study design will be documented in subsequent versions of this protocol and reported transparently in publications arising from the study.

This more accurately reflects the intended meaning and removes any implication of a separate registration. The original wording appeared in the Study Design section.

Recruitment and informed consent

Reviewer comment:

The reviewer requested additional detail regarding provision of study information, voluntary informed consent, time to consider participation, potential perceptions of coercion associated with the embedded researcher role, and recruitment of patients with cognitive or communication impairments.

Response:

Thank you. We agree that this aspect of the protocol would benefit from greater procedural detail. We have therefore added a dedicated Recruitment and Consent subsection.

The revised section describes provision of written study information, subsequent explanation of the study by a researcher, the opportunity to ask questions and consider participation before consent is obtained, and the voluntary nature of participation. It also makes clear that participation or non-participation will not affect clinical care or staff employment/professional relationships.

A prescribed formal cooling-off period was not a feature of the approved protocol and we have therefore not retrospectively introduced one. Instead, we have clarified that potential participants have an opportunity to consider the information and ask questions before deciding whether to participate.

The consent procedures described are consistent with the study as subsequently conducted, in which potential patient participants received study information before researcher contact and were allowed time for consideration prior to consent.

Recruitment of patients with cognitive or communication impairment

Reviewer comment:

The reviewer asked for clearer consideration of how cognitive and communication impairments would be managed during recruitment and data collection.

Response:

Thank you. The protocol already included provisions for supported participation, but we agree that these should be more prominent within the recruitment and consent process.

We have therefore strengthened the cross-referencing between the Eligibility Criteria and Recruitment and Consent sections. The manuscript clarifies that the presence of a cognitive or communication impairment does not in itself result in exclusion. Existing hospital-approved communication supports, including communication passports, augmentative and alternative communication aids and family/carer-supported participation, may be used where appropriate. Exclusion occurs only where available supports are insufficient to enable valid consent and meaningful participation and to elicit the patient's own view.

Organisation and sequencing of the Methods

Reviewer comment:

The reviewer observed that some questions arising during the initial reading were answered later in the manuscript and suggested that some resequencing might improve flow.

Response:

We agree and thank the reviewer for this helpful observation. Rather than substantially restructuring the Methods section, which broadly follows the sequence of the study, we have improved signposting and placed recruitment and consent information in a dedicated subsection adjacent to the eligibility criteria.

We have also added clearer cross-referencing from Study Design to the subsequent Qualitative Data and Data Analysis sections so that readers are directed to the relevant methodological detail when each component is first introduced.

This addresses the reviewer’s concern while avoiding unnecessary duplication of methodological information already provided later in the manuscript. The reviewer similarly noted that several initial queries were answered as the manuscript progressed.

Abbreviations

Reviewer comment:

The reviewer recommended consistent use of abbreviations such as MDT, IDT and NRH after the terms have first been defined.

Response:

Thank you. We have reviewed the manuscript and standardised the use of abbreviations throughout following their first definition.

Availability of datasets

Reviewer assessment:

Datasets were rated as only partly presented in a usable and accessible format.

Response:

We note that this article reports a study protocol rather than study findings. Consequently, no study dataset is associated with the protocol article. The Data Availability statement therefore remains:

No data are associated with this article.

The protocol currently states this explicitly.

Overall comments

Reviewer comment:

The reviewer considered the study clinically relevant and well-motivated and suggested that additional methodological detail would strengthen the protocol.

Response:

We thank the reviewer for these constructive comments. We believe that the revisions have improved the clarity and transparency of the protocol while preserving its prospective nature. The protocol was developed and published before data collection commenced; accordingly, the revisions clarify the originally planned study rather than retrospectively altering the protocol to reflect subsequent implementation changes. The later study manuscript explicitly records that the protocol preceded data collection.

We thank the reviewer again for the careful reading of the manuscript and for the suggestions, which have improved both the methodological clarity and navigability of the protocol.

HRB Open Res. 2026 Jul 29. doi: 10.21956/hrbopenres.15995.r56724

Reviewer response for version 2

Yuho Okita 1

All the questions raised earlier have now been addressed and answered.

Is the study design appropriate for the research question?

Partly

Is the rationale for, and objectives of, the study clearly described?

Partly

Are sufficient details of the methods provided to allow replication by others?

Partly

Are the datasets clearly presented in a useable and accessible format?

Partly

Reviewer Expertise:

NA

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

HRB Open Res. 2024 Dec 27. doi: 10.21956/hrbopenres.14985.r43546

Reviewer response for version 1

Yuho Okita 1

I have several questions and points of clarification regarding your research:

Research Questions: While I can see that research questions 1–3 can be addressed through the qualitative aspects of your mixed-methods approach, what specific research question are you trying to answer with the quantitative aspects?

Goal Setting Process: In the abstract, you mentioned: "The goal-setting process was collaboratively designed based on iterative rounds of patient and staff feedback." Does this mean the goal-setting process has already been developed in prior work, and this study aims to refine that process through additional research?

Qualitative and Quantitative Rationale: You highlighted the rationale for using qualitative methods by stating: "By capturing staff and patient experiences using multiple and mixed methods, we can gain insight into the phenomenon of shared decision-making, IDT goal setting from different perspectives, as well as barriers to implementation in this context." However, why is there also a need for quantitative methods? Where is the specific rationale for including this aspect?

Recruitment and Eligibility: Who will be responsible for recruiting participants and determining their eligibility?

Previous Research: You wrote: "The new goal process was developed in response to feedback from and in collaboration with NRH staff and patient representatives." Was this process developed in your previous research?

Clarify Researcher Roles: For the analysis section, you mentioned that the lead researcher will conduct the analysis. This needs to be clearly stated in other sections, such as recruitment and participant eligibility determination, to ensure consistency and clarity.

Definition of "Staff": What does “staff” refer to in this context? Are you including rehabilitation practitioners, carers, doctors, nurses, or other groups?

Overall Aim of the Research: I did not fully grasp the overall aim of this research. Are you testing the already-developed goal-setting process from a previous study with the intent to refine it? Or are you exploring participants' experiences of current shared decision-making practices to identify areas for improvement? Or is it a combination of both?

Is the study design appropriate for the research question?

Partly

Is the rationale for, and objectives of, the study clearly described?

Partly

Are sufficient details of the methods provided to allow replication by others?

Partly

Are the datasets clearly presented in a useable and accessible format?

Partly

Reviewer Expertise:

NA

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however I have significant reservations, as outlined above.

HRB Open Res. 2026 Jul 6.
Áine Carroll 1

Comment 1: Research questions and the quantitative aspects. “What specific research question are you trying to answer with the quantitative aspects?”

Response: This was underspecified in the original submission. We have added a sentence following Research Question 2 clarifying that the quantitative measures (ISVS-9B, NoMAD) provide standardised, repeated-measures data on staff interprofessional socialisation and process normalisation, which complements the qualitative interviews by allowing us to track group-level trends over time and to triangulate these trends against individual staff narratives. This addition appears in the “Research questions, aims and objectives” section.

Comment 2: Was the goal-setting process developed in prior work?

Response: Yes, and we agree this was not made explicit. We have added a clarifying statement at the start of the “Intervention” section noting that the new goal-setting process was developed prior to, and separately from, the current evaluation study, through a quality improvement initiative led by the NRH’s IDT Quality Care Team in collaboration with staff and patient representatives. The present protocol concerns the evaluation of that process, not its development.

Comment 3: Rationale for quantitative methods alongside qualitative.

Response: We have expanded the rationale in the “Study design” section to explain that the quantitative and qualitative strands serve complementary purposes: qualitative interviews provide depth of understanding of individual experience, while quantitative measures allow us to track standardised change over time across the full staff group and to assess feasibility for a future hospital-wide impact evaluation. We have also added a description, in the Data analysis section, of how the two strands will be integrated at the interpretation stage.

Comment 4: Recruitment and eligibility responsibility.

Response: We have added a sentence to the “Eligibility criteria” section clarifying that recruitment and eligibility screening will be carried out jointly by the embedded researchers (LC, ZT) and clinical staff (e.g. the named keyworker or team coordinator) on each participating unit.

Comment 5: Was the goal process developed in the authors’ previous research?

Response: As above (Comment 2), we have clarified that the process was developed through a separate, prior quality improvement initiative at NRH, not through prior academic research by this author team. We have added detail on who was involved in that development (staff across disciplines and patient representatives, coordinated by the IDT Quality Care Team).

Comment 6: Consistency in describing researcher roles.

Response: We have added a sentence to the “Study design” section stating that the embedded researchers (LC, ZT) hold primary responsibility across recruitment, data collection and analysis, working alongside clinical staff for participant identification, so that this is stated consistently rather than only in the analysis section.

Comment 7: Definition of “staff”.

Response: We have added a definition to the “Eligibility criteria” section: for this study, “staff” refers to clinical and allied health professionals directly involved in patient care and the goal setting process on participating units (medical, nursing, health care assistant (HCA) and health and social care professional (HSCP) staff) and does not include non-clinical or administrative staff.

Comment 8: Overall aim of the research.

Response: We recognise the original text did not make sufficiently clear that this is a combination of both evaluating the already co-designed process and exploring current staff/patient experience of shared decision-making practice as it is now being used. We have revised the closing paragraph of the introduction and the opening of the “Research questions, aims and objectives” section to state explicitly that the study aims (a) to evaluate staff and patient experience of the process as implemented, and (b) to use this evaluation to identify barriers and enablers that can inform iterative refinement and future hospital-wide rollout.

HRB Open Res. 2024 Dec 26. doi: 10.21956/hrbopenres.14985.r43547

Reviewer response for version 1

Lesley Scobbie 1

Pilot of a person-centred, interdisciplinary approach to goal setting in Ireland’s National Rehabilitation Hospital: a study protocol

The outlined study seeks to use a mixed methods approach to evaluate the introduction of a tailored, shared decision-making, interdisciplinary goal setting process with a mixed diagnostic group of patients in an inpatient rehabilitation setting in Ireland, including identifying barriers and enablers to its implementation.

General points:

> Avoid use of too many abbreviations as it gets confusing for the reader.

> There are many different concepts being evaluation in this study – interdisciplinary teamwork, shared decision making, person-centred care, goal setting and implementation. Each of these concepts should be defined (some are) and how they will be evaluated unpacked on an individual basis.

> No details have been provided re. staff training to use the new goal setting approach - this is a significant omission. 

Abstract:

Would have been helpful to write IDT in full i.e. interdisciplinary team, as it is not clear what it stands for within the abstract.

Introduction:

Para2: Write MDT in full at first mention.

Clear definition of Multi-Disciplinary Team would be helpful in the introduction.

Methods:

Re. Eligibility criteria – “Patients will be excluded if they have severe cognitive or communication impairments resulting in the inability to participate in the interview”

To optimise inclusivity, are there any supports that can be put in place to support people with cognitive and / or communication difficulties to participate in this research?

Re. Sampling - What kind of sampling method will be used to inform patient and staff recruitment?

Re. Intervention – Are there any details about how the new goal process was developed? How many staff and patients were involved in its development and who were they?

As noted in the introduction, goal setting approaches have been developed and reported e.g., Scobbie et al 2020; Van De Weyer 2010; Doig et al 2023.  It would be helpful if the authors could justify development of their own approach rather than build on one of those already developed.

Figure 1 is helpful but does not fully describe the new goal setting approach.

For example,

  • What is the information booklet that is given out pre admission. Will there be a different one for each specialty?

  • How will an individual’s readiness/ desires to lead own goals? Would it not be appropriate at times for a staff member to lead if the patient is struggling/ overwhelmed/ lacking confidence?

  • What are the recognised tools and accessible support proposed for use at a meet the team session?

  • Should the patient not be involved in deciding what is required to support progress towards their goals (given it is a person centred approach)?

  • Team and family feedback on goal outcomes; should the patient be involved oi this too?

  • Would TiDIER have been a better way to describe the intervention? https://www.equator-network.org/wp-content/uploads/2014/03/TIDieR-Checklist-PDF.pdf?

Re. Data Collection

“(C-Cogs and CollaboRATE) will be administered shortly after the initial goal setting meeting”

It is unclear from Fig 1. what this meeting is – meet the team/ goal setting conference?

Will there be support available if for any reason patients find these measure difficult to complete?

Will and if so, how will the qualitative and quantitative data be combined/ compared/ joined?

Re. Public and Patient Involvement – it is notable only two patients were involved (no info given re their background/ level of involvement) and no carers. Given this goal setting process may be used with a variety of patients with different ages/ diagnosis - this seems to be a small number.

Is the study design appropriate for the research question?

Partly

Is the rationale for, and objectives of, the study clearly described?

Yes

Are sufficient details of the methods provided to allow replication by others?

No

Are the datasets clearly presented in a useable and accessible format?

Not applicable

Reviewer Expertise:

goal setting, stroke rehabilitation, implementation

I confirm that I have read this submission and believe that I have an appropriate level of expertise to state that I do not consider it to be of an acceptable scientific standard, for reasons outlined above.

HRB Open Res. 2026 Jul 6.
Áine Carroll 1

General points

Abbreviations: We have reviewed the manuscript throughout and expanded abbreviations at first use that had not previously been defined (notably HCA and HSCP), while retaining abbreviations that are standard and necessary for readability (e.g. NRH, IDT, EPR) once defined.

Multiple concepts requiring individual definition: We agree that interdisciplinary teamwork, shared decision-making, person-centred care, goal setting and implementation/normalisation are distinct constructs. We have added or sharpened definitions for each on first use in the Introduction, and have clarified, where each construct is operationalised, which specific measure or interview topic captures it (see Methods).

Staff training omission: This was a significant gap, and we thank the reviewer for identifying it. We have added a new subsection describing staff training delivered prior to implementation, covering the documentation, the underlying principles of person-centred and shared decision-making practice, and use of the pre-admission information booklet, delivered via team-based workshops facilitated by the IDT Quality Care Team.

Abstract

We have spelled out “interdisciplinary team (IDT)” in full at first mention in the Abstract.

Introduction

We have written “multidisciplinary team (MDT)” in full at first mention (paragraph 1) and added a short comparative definition distinguishing MDT and IDT working, so that the abbreviation used later in paragraph 2 is already defined.

Methods

Eligibility criteria / inclusivity for patients with cognitive or communication impairments: We have added a statement describing supports that will be offered to patients with mild-to-moderate cognitive or communication difficulties who do not meet exclusion criteria, including additional time, Easy-Read materials, communication aids, and involvement of a family member or carer to support participation.

Sampling method: We have added a short statement specifying that a convenience sampling approach will be used for both staff and patients, given the relatively small potential participant pool across the three pilot units.

Development of the new goal process / justification relative to existing frameworks: We have added a paragraph to the “Intervention” section acknowledging the existing frameworks the reviewer notes (G-AP, the keyworker-led model, the role-based IDT approach) and explaining that, consistent with evidence that complex interventions are best tailored to local context (Craig et al., 2013, already cited), the NRH team elected to co-design a context-specific process informed by, but not a direct replication of, these frameworks, reflecting NRH’s mixed case-mix and its concurrent transition to an electronic patient record.

Figure 1 clarifications: We have added explanatory text addressing each point raised: - The pre-admission information booklet: a core version is used hospital-wide, with programme-specific inserts for each speciality (stroke, ABI, SCSC, POLAR, paediatric). - Readiness to lead own goals: we clarify that a staff member may take a more directive lead where a patient’s readiness or capacity is limited, with the explicit aim of increasing patient control as capacity develops. - Recognised tools and accessible supports: we now specify examples (Easy-Read materials, communication charts/boards, interpreter or speech and language therapy input) selected according to individual need. - Patient involvement in support planning: we clarify that patients and families are invited to contribute to decisions about the tasks/activities/timetable required to support progress towards their goals. - Family feedback on goal outcomes: we clarify that patients and families are involved together in this feedback at the pre-discharge meeting.

TIDieR checklist: We agree this is a useful reference point for intervention reporting and have added a note in the Intervention section that the description follows relevant elements of the TIDieR checklist (Hoffmann et al., 2014) to support replicability, while retaining our narrative + figure format so as not to substantially restructure the protocol.

Data collection, meeting terminology. We have clarified that the “initial goal setting meeting” referred to in the measures section corresponds to the goal, action and care planning (goal setting conference) meeting shown in Figure 1.

Support for patients completing self-report measures: We have added a statement that the embedded researcher will offer support (reading items aloud, additional time, or recording responses on the patient’s behalf) without altering item content or interpretation, for patients who require it.

Combining/joining qualitative and quantitative data: We have added a statement to the Data analysis section describing that the two strands will be integrated at the interpretation stage using a mixed-methods triangulation approach, with joint displays used where relevant to explore convergence or divergence between self-report measures and interview themes.

Public and Patient Involvement: We have expanded this section to give brief, anonymised background on the two patient co-researchers’ prior admissions and have added an explicit acknowledgement that PPI in this phase was limited to two individuals with lived experience and did not include family carers, with a commitment to broadening patient and carer involvement in the subsequent hospital-wide implementation study.

We thank the reviewer for their thorough and helpful engagement with this protocol, which we believe has considerably improved the clarity and rigour of the study design.

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Data Availability Statement

    No data are associated with this article.


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