Diversity of formats and purposes
Interviewees described delivery of remote group-based care in different formats (Box 2). The term VGC was used interchangeably regardless of whether individually-focused clinical consultations took place in the group setting (which is usually the key prerequisite for a session to be described as a ‘group consultation’ according to published literature and the NHSE/I-commissioned training).
VGC type | Characteristics |
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Clinical | One-to-one clinical discussion on test results, medication, and self-management in the group setting, combined with peer support and discussion |
Educational | Focusing on self-management or ‘healthy living’ topics, with little or no individual clinical input |
Informational | Webinar format rather than clinical consultation, usually involving a large number of attendees |
Mixed | Combining elements from the first three types |
Box 2. Remote group-based care formats
All formats included formal components, such as structured annual reviews for long-term conditions, and informal components, such as patient-driven, open discussion. They were delivered as scheduled sessions where patients with a relevant condition could book into standard slots or in a targeted way, inviting patients with specific clinical and/or social needs such as vulnerable new families (even across different practices). Patient participation was either periodic, to match annual or 6-monthly review requirements for chronic conditions, or more regular, with patients joining multiple, sometimes consecutive, sessions (with the same or different groups). Staff who were interviewed delivered VGCs primarily using clinical or mixed formats across a range of conditions and needs, including for patients with diabetes, asthma, chronic obstructive pulmonary disease (COPD), cancer (acute treatment and long-term survivors), mild COVID-19, anxiety, those with postnatal care needs, and those receiving healthy eating support.
The NHSE/I-commissioned training (initiated in April 2020) recommended that clinically focused VGCs involve at least two members of staff (a facilitator and a consulting clinician). VGCs would start by welcoming patients, confirming their identities, explaining confidentiality, and acquiring verbal or written consent. The session (lasting 1–1.5 hours) would then continue with the clinician consulting individually with each patient in the group setting, drawing on the ‘results board’: usually a PowerPoint slide, shared on the screen for everyone to see, with a table including clinical, self-management and/or quality-of-life information for each patient (depending on condition and review requirements). This was either completed in advance (for example, through blood test results) and/or during the session (for example, using questions such as ‘have your symptoms affected usual activities?’). In some VGCs on more sensitive topics clinicians decided not to share the board (for example, in postnatal mental health groups). Following individual consultations, the groups usually continued with open discussion and questions on concerns and self-care needs, and sessions ended with patients consolidating learning and personal goals.
Clinical and non-clinical staff who participated in training (roughly two to four staff members per participating practice) described programme support and inter-organisational learning as instrumental:
‘ [The programme] has been quite useful because we’ve had training put in place, which has enabled us to quickly train up facilitators that we thought we were going to have to train in-house.’
(Interview 10, GP)
Finding the ‘right’ VGC format was not without challenges, especially at early stages when practices were experimenting with remote options. Delivery of clinical and mixed formats required a bigger operational and cultural shift from usual care practices; therefore, many practices decided to stay within the relative ‘safety’ of informational or educational sessions.
This study’s longitudinal focus on the two GP sites was mainly driven by how they evolved their group-based care models to deliver primarily clinical (rather than informational or educational) content (see Box 1).
Relationship-focused care in VGCs
Establishing (online) rapport
Staff interviewees discussed VGCs (particularly ones with clinical focus) as having the potential to both strengthen and fragment caring relationships among patients, clinicians, and the practice team. In the early stages, staff worried that their VGCs appeared ‘scripted’ (Interview 18, receptionist/VGC facilitator) and that it would be difficult to establish rapport and patient interaction online compared to face-to-face group consultations:
‘Normally when you’ve got a [face-to-face] group consultation, you work the room, a bit like an actor or a comedian […] you kind of get the feel for how is it going, what’s going down well, what isn’t, when are they looking puzzled […] it’s really hard to keep talking when you’re not getting any non-verbal feedback.’
(Interview 2, GP)
Some patients expressed how they were more reticent to share initially, especially when they had faced a significant illness burden (but became more open in subsequent VGCs, having listened to others discussing their personal circumstances). One patient with diabetes (who declined the invitation to join VGCs) explained she did not feel the need to share with a group and saw the process as inefficient, expecting many discussions to be unrelated to her own circumstances:
‘I’m not really a great joiner-in. I would class myself as not social in that kind of way. I tend to be an individual in terms of getting things done and not wanting to hang out with lots of people, to be honest […] those [the one-to-ones] I find very efficient. They’re targeted, they’re focused, I get the information that I need and I believe [the clinicians] get the information they need.’
(Interview 26, patient)
Relying on pre-existing and new relationships
Having a pre-existing relationship with patients allowed staff to better manage the perceived distance introduced by the online format as they understood how to focus clinically on things that mattered to them. If this relationship was not in place already, clinicians spent time going through medical records for clues on how best to guide the discussion. Where clinicians did not achieve in-depth understanding or when complex individual needs arose in the pandemic, VGCs sometimes led to fragmentation in the care relationship, and the need for additional encounters:
‘I have an ileostomy, so I was asking some questions and the lady who was running it didn’t really understand what I was trying to ask […] it was fine because we did a session separately afterwards which I then sent some information in advance so she could understand … ’
(Interview 16, patient)
With time, staff found they were better able to facilitate patient relationships and discussion (even if patients had never met each other before, although in a few cases relationships developed between repeat attenders), which increased the value of VGCs:
‘ […] now we know what we’re doing; we’ve relaxed a little bit. I feel like that’s obviously come across to the patients as well. So in the last couple it’s been really good patient interaction. There’s been times where we literally can just sit back and just let them there, just having a chat […] ’
(Interview 18, receptionist/VGC facilitator)
Patients valuing access and connection
The pandemic context appeared to facilitate VGC implementation as many patients and staff became more receptive owing to lockdown and restrictions, disruption to patient support groups, and a shift towards remote interaction: ‘ it feels much more natural than it would have done before COVID’ (Interview 22, patient). Patients who chose to take part in VGCs preferred the convenience of participating online, particularly as those shielding wanted to avoid the ‘anxiety of being in a public place’ (Interview 21, patient). A patient with mobility issues mentioned how it had been a ‘bit of a nightmare’ getting wheelchair-accessible parking, and that remote participation made her ‘feel more independent’ (Interview 16, patient). Others did not have to take time off work or worry about childcare as they could attend remotely.
One of the patients (a retired health professional) talked about feeling more connected to the practice through engagement in VGCs, as the nurse came to know his situation better and had a more direct relationship with him, rather than only knowing him through his ‘medical records’, which he described as ‘personal [but] not personalised’ (Interview 21, patient). His comments pointed both to an increased level of access and to increased depth in the clinical relationship (‘it makes it easier and more personal I think that I can phone [the nurse] up and she knows’ [Interview 21, patient]), which may, however, become unsustainable if larger numbers of patients participate in VGCs.
Patients also came to value ‘human connection’ (Interview 22, patient) , especially when sharing experiences of treatment with peers, and (despite initial reticence from some) they expressed feeling comfortable sharing with others with the same condition:
‘ [the other patient] said how much he felt for me because I’d not started my 6 weeks of radiotherapy, and he hoped it would go well. And when I was sort of three-quarters of the way through, he remembered what I was going through and asked me how it was, and that’s a really nice human connection.’
(Interview 22, patient)
Challenges with digital inclusion
It is likely that sessions primarily involved patients with good IT skills. Practices attempted to simplify the remote joining process but there were still patients who faced difficulties, and concerns remained regarding access for those without IT equipment, bandwidth, or confidence to use technology for VGCs.
Using VGCs to address organisational priorities
Staff motivations for setting up VGCs
Some practitioners presented VGC implementation as a next step (albeit not easy) from their face-to-face group consultations programme, as they started to manage the majority of clinical work remotely in COVID-19. Others faced a steeper learning curve as they began remote delivery and group-based care at the same time.
Across practices, motivations for setting up VGCs were primarily demand-led (for example, in a practice so overwhelmed they had adopted a telephone-first triage approach long before the pandemic) and performance-driven (for example, to meet Quality and Outcomes Framework [QOF] requirements for income generation):
‘I’m hoping that what it will achieve is that we will keep our QOF ticking over. Obviously, that is still a big part of our income and if we took a big hit on QOF then that is very destabilising for the practice.’
(Interview 2, GP)
Staff interviewees also spoke about setting up VGCs to increase patient access in the context of GP workforce recruitment and retention challenges, support COVID-19 recovery, improve patient satisfaction and experience, enable a ‘coaching’ approach to patient care, achieve better quality clinical consultations, and address isolation in living with chronic illness, compounded by lockdown and the pandemic. Most clinicians and patients suggested that they did not experience an increased need for follow-up after VGCs in a way that would burden the practice.
Workload and practice commitment
Many staff participants acknowledged that setting up and delivering VGCs required significant time commitment (about half-day preparation per VGC) and changes to administrative processes. Operational work involved sending invitations and reminders, supporting patients to join the video call, reviewing and updating records, preparing materials, issuing prescriptions, and following up on any individual queries. Introducing this new remote model of group-based care required practice-wide support at all levels, to be able to free up resources and distribute the workload:
‘ […] we started where we thought maybe I could do it whilst I was on reception […] but we realised rather quickly it’s just not going to work. We needed to have dedicated time […] ’
(Interview 18, receptionist/VGC facilitator)
‘They needed to have at least a champion GP […] who could unblock the drain in their practice to get them the resources and time to do it. And the second person who was key was the practice manager, and if both of those people weren’t on board then you could just forget it.’
(Interview 8, VGC training lead)
Enabling relational coordination in practice
VGCs required staff working together or coordinating across rotations to set up and deliver different sessions. In site A the practice pharmacist was supported to different degrees by the nurse manager, healthcare assistant, IT officer, receptionist, medical student, and others. In site B the practice nurse, who had significant autonomy and scope in her role, was supported by a receptionist/VGC facilitator, as well as other NHS and third sector staff (for example, Macmillan nurses and physiotherapists). This need for collaborative practice meant a shift away from traditional hierarchical working and a re-thinking of professional culture in service delivery:
‘ […] it’s hard to address those cultural issues and it’s a very different way of working. For the team [I want to achieve] better team work, more even stevens, you know, less doctors up here and everyone else down there. So, everyone working together […] ’
(Interview 11, GP)
Extending roles and skillset on remote group-based care
Enthusiastic staff (clinical and non-clinical) were prepared to make significant effort so that VGCs would work in their practice, and found the experience rewarding. Some suggested that they extended their skillset and were able to take on additional leadership, clinical, or operational responsibilities, such as IT staff taking front-end roles to support patients, receptionists delivering group facilitation, and healthcare assistants learning about diabetes:
‘They’ve learnt an awful lot the two healthcare assistants who are doing this; they’ve learnt a lot about diabetes. […] We’ve learnt a lot. I learn from the patients because we’re a very multi-ethnic area. I learn an awful lot about things from patients and some of it I’m quite shocked about.’
(Interview 25, nurse manager)
Other staff, however, seemed more reticent to engage with this model, including those who received VGC training but later refrained from taking on any VGC responsibilities. This was primarily because of a lack of time and organisational slack, and the complexity of group-based care:
‘So, we have members of the team that have been trained and they’re taking it in turns […] everybody’s rotating, so it’s not too much work for one person. There has [sic] been a few emails back saying, “I haven’t got time for this,” and so on […] it’s all very time consuming.’
(Interview 10, GP)
IT and infrastructure challenges
Supporting patients to access the video platform involved significant background work, as one of the receptionists explained: ‘patients that need a little bit of help, just give them a call and just talk them through how to just to get onto the meeting and things like that’ (Interview 18, receptionist).
Early in the pandemic, some practices faced IT equipment shortage, which meant not all staff could access webcams. Network bandwidth was a barrier to remote care in some practices (although this improved with time).
The video platform used to deliver VGCs (MS Teams) brought challenges as some of its features and integration with practice systems were difficult to configure and changed over time. Staff reflected that such technical problems looked ‘unprofessional’ (Interview 10, GP), and could influence patient engagement with group-based care:
‘ […] a lot of our patients said that they didn’t receive the email. And some of the patients were in the lobby and they couldn’t get in […] some people weren’t getting a chat box, so they had to keep going out and trying back in again […] that looked a bit unprofessional at the beginning […] ’
(Interview 10, GP)
In co-design workshops, participants shared several ideas on improving technology-supported group-based care, including on the physical space and recording systems required at practice level, best approach to managing technical glitches and lack of digital confidence, and support required at the patient end (Figure 2).
Figure 2. Post-it notes by participants in co-design workshops presenting ideas on improving video group consultation delivery. IG = information governance. PROM = Patient Reported Outcome Measures. VC = video consultation.
Balancing concerns on patient risk and information governance
Governance around remote care was partly relaxed in the COVID-19 context. However, VGCs raised new ethical concerns around online confidentiality, consent, and risk that the national VGC programme sought to address. As this resulted in a short pause to programme delivery, some clinicians made their own local clinical safety judgments, balancing concerns about confidentiality with the need to address safeguarding issues in their locality:
‘ […] we’ve taken the decision not to pause because we have indemnity cover from NHS, well we have from the MPS [Medical Protection Society]. And also the other decision that we didn’t pause is because when we had safeguarding issues in our area; we have shaken babies.’
(Interview 10, GP)