- Open Access
Developing good practice indicators to assist mental health practitioners to converse with young people about their online activities and impact on mental health: a two-panel mixed-methods Delphi study
BMC Psychiatry volume 22, Article number: 485 (2022)
Online activity has been linked to poor mental health in children and young people, particularly those with existing vulnerability who may inadvertently or otherwise access harmful content. It is suggested health and social care practitioners should address online activity during mental health consultations, but guidance about acceptable or effective ways to do this is lacking. This study sought to derive good practice guidance to support mental health practitioners to engage young people in conversations about their online activities and impact on mental health.
A mixed-methods Delphi (consensus) study was conducted with a panel of mental health practitioners (n = 21) and a panel of young people (n = 22). Practitioners worked with children or young adults in the UK, mostly in statutory services (80.9%), in varied clinical roles, with 2 – 30 years of experience and most were female (87.5%). Young people were mostly female (77.3%), 13—22 years old, reported varied mental health diagnoses and had sought help from services. Across 3 rounds, panellists completed questionnaires which involved rating agreement with statements and answering open-ended questions. Iterative analysis informed subsequent questionnaire content. The percentage of participants rating their level of agreement with each statement was calculated. The threshold for inclusion as a good practice indicator (GPI) was 75% across both panels. Thematic analysis was used for free-text data.
Twenty-seven GPIs emerged covering ‘who’ (which young people) should be asked about online activities, ‘when’, ‘what’ should be discussed, and with what ‘outcome’. Panels agreed conversations should be initiated with all young people from first meeting and regularly thereafter, with ‘red flags’ indicating a conversation may be pertinent. Core topics were identified with additional areas for patients presenting with disordered eating or self-harm. Panels emphasised conversations should be fluid, normalised, and encourage reflection and self-awareness.
Mental health practitioners could empower young people to exercise agency in relation to online safety and capitalise on positive features. Findings also identify training needs for practitioners. Further research should explore real-world application of the GPIs and transferability to underrepresented groups within our panels, such as males and younger children. Ethnicity and deprivation were not recorded.
Social media and internet use have been linked to poor mental health in children and young people by a significant body of empirical literature of varying study designs . Areas of concern include sense of self, body image and disordered eating , socioemotional functioning , sleep disturbance , and self-harm and suicidality [5, 6]. Yet, positive impacts are also described, such as improved social connectedness and support, and there is recognition that effects may vary according to the characteristics and circumstances of the young person, including their existing vulnerability . This is of import given the ubiquity of device ownership amongst children, adolescents and young adults.
Actions to tackle online harm focus on legislation to increase the responsibilities of platforms and providers and school-based online safety education . A role for health and social care practitioners in addressing online activity during consultations has also been intimated [1, 9, 10], with suggestion this could involve harm reduction by recommending reduced usage, encouraging parental involvement, discussing risks and sleep hygiene, use of motivational interviewing to reduce excessive usage, promotion of digital citizenship and incorporation of online safety into crisis planning. In 2019, the UK Royal College of Psychiatrists  recommended psychiatrists should routinely ask about technology use when undertaking mental health assessments with children and young people.
Preliminary evidence indicates asking patients about their online activity may be clinically beneficial. For instance, in a qualitative study, psychiatric liaison clinicians reported that exploring online behavior with patients presenting following self-harm could contribute to assessment of risk by deepening understanding of the individual, and identifying motivations behind suicidal behavior, active suicidal intent and disguised requests for help . However, some clinicians were reticent to ask in case this prompted patients to access ‘bad’ content and some sought guidance about how to respond to disclosures of harmful use. While it is likely that such conversations increasingly take place within consultations, guidance about how to conduct these is lacking. In our scoping research (unpublished observations: Rifkin-Zybutz, Derges, Biddle et al.), 93% of 86 child and adolescent mental health practitioners surveyed reported having no access to a protocol to guide discussion around online activities with young patients, 76% had received no training or guidance, only 54% covered this topic routinely and 71% expressed a wish for training. Alongside these data, many adolescents reported a lack of satisfaction where such conversations had taken place as part of their care due largely to a sense of feeling judged. Despite this, 92% of practitioners and 68% of young people surveyed agreed health and social care practitioners should contribute to ensuring the safety of young people online and 73% of practitioners believed exploring online use should form an essential part of risk assessment.
This study aimed to identify good practice indicators to inform development of guidance to assist mental health practitioners to engage young people in acceptable, safe and useful conversations about their online activities and how these impact on their mental health. Consensus was achieved by using a two-panel, three-stage Delphi method, drawing upon the expertise of child and adolescent mental health practitioners and young people with lived-experience of mental health problems and service use.
This study was part of a wider programme of research investigating young people’s digital technology in the context of mental health consultations and management of risk. The Delphi method is used to systematically determine expert consensus. It is of proven utility in mental health research  and has been used to explore areas similar to that considered here . We used a mixed-methods design. This involved: 1) using findings from prior engagement research to develop an initial Delphi questionnaire; 2) three iterative rounds of quantitative and qualitative data collection across two panels (mental health practitioners and young people); 3) development of good practice indicators.
The Delphi questionnaire was informed by research conducted in the UK with young people aged 13–24 years and mental health practitioners who worked with children or young people. This comprised a series of online surveys, focus groups and semi-structured interviews to clarify the importance of the topic to both groups and to identify dimensions to investigate within the Delphi. The resultant questionnaire was shared with three practitioners and a young person’s research advisory group member, who suggested refinements to improve clarity and ensure the language used was accessible. This process is detailed in an additional file [Additional File 1].
The Delphi process
A panel of practitioners (PP) and a panel of YP (YPP) were recruited by advertising on Twitter, via UK-based third sector organisations, within networks established during our engagement phase, and through snowball sampling. Potential participants completed a brief online screening questionnaire and, if eligible, were invited by email to take part. Eligible practitioners were health or social care professionals currently working in young people’s mental health services. Eligible YP were aged 12–24 years with experience of using mental health services. Recruitment was open for 6 weeks. Participants became panel members upon completing questionnaire 1.
All questionnaires were administered online and completed anonymously. Informed consent was provided at the start of questionnaire 1, including parental consent for under 16s. The Round 3 questionnaire was sent to all panel members irrespective of whether they completed Round 2. Questionnaires contained a mix of i) statements to be rated for agreement using a 5-point Likert scale (strongly disagree, disagree, neither agree nor disagree, agree, strongly agree) and ii) open-ended questions and free-text boxes for further comments. The questionnaires for Rounds 2 and 3 differed by panel according to the specific views previously obtained in each (below). The entire Delphi took place between December 2020 and April 2021. A shopping voucher was offered as a gratuity on completion of each questionnaire.
Analysis took place after each round to enable an iterative approach, the next round being used to clarify, develop and refine emerging perspectives. Findings for each panel were analysed separately (not pooled) to highlight areas of difference and similarity. Quantitative data were analysed in Stata v.16. The number and percentage of participants rating their level of agreement with each statement at each point on the scale was calculated to examine the level of similarity among participants (consensus). Guided by other studies , statements were considered to have reached consensus when 75% or more of the panel either agreed (rated statement as strongly agree or agree) or disagreed (rated statement as strongly disagree or disagree). Stability was considered for items repeated over two rounds and not reaching the consensus threshold. The percentage shift between rounds was calculated across the three main categories of response (strongly agree/ agree; unsure; disagree/ strongly disagree). Items with a shift of less than 10% across all categories were considered to have reached ‘stable non-consensus’. Qualitative free-text data were coded inductively using thematic analysis to identify themes. LB and JD coded independently then compared findings. Similar ideas were grouped together into conceptual categories.
In Round 2 and 3 questionnaires:
Statements that had reached consensus were not repeated. Statements without consensus were repeated with the panel’s previous round of results shown as aggregate percentages expressing current agreement, disagreement and uncertainty, and a summary of any relevant free-text data expressing arguments for and against the statement;
Statements showing stable non-consensus across Rounds 1 and 2 were removed from Round 3 on the basis this indicated the panel could form no clear view;
Open-ended questions were added to gain further detail around accepted statements, or nuance where consensus could not be reached within or across panels. Equivalent questions were asked of each panel;
New statements were added following qualitative analysis of free-text and included for both panels to ensure they were rated by both groups.
Identification of good practice indicators
Agreement rates for each statement were tabulated and compared across panels. Statements that reached consensus in both panels were progressed for possible inclusion as Good Practice Indicators (GPIs). Where statements were agreed early in the Delphi and then superseded by more precise follow-on statements, only the latter were retained. Lists of statements—such as ‘red flags’ indicating when practitioners should ask about online activities—were grouped and presented as a single overarching statement with accompanying sub-items. Other related statements were also merged. Statements about practitioner support needs were not regarded as GPIs and were noted separately.
Statements reaching consensus in one panel but not the other were then considered. These were identified as ‘near-misses’ where the second panel expressed a majority trend in the same direction as the panel with consensus, or as ‘conflicts’ where the majority trend was opposing. The strength of the near-miss or conflict was then ranked according to the majority percentage in the second panel as low (50–59%), medium (60–69%), or high (70–74%). Information from near misses and conflicts, and insights from free-text data, were used to inform a supporting commentary.
From a total pool of 44 practitioners and 40 young people, 41 and 38 respectively were eligible and invited to participate. We recruited 21 practitioner panel (PP) members and 22 young people panel (YPP) members (Table 1). All were based in England or Wales covering urban and rural settings. Practitioners were mostly females (87.5%) working in the statutory sector (80.9%) but represented a range of clinical roles and years of experience. The YPP were diverse in age, diagnoses and experience of service use. Three-quarters were female. Ethnicity and deprivation were not recorded. Retention rates were: 76% (PP) and 95% (YPP) in Round 2; 71% (PP) and 73% (YPP) in Round 3.
Each panel rated 135 statements; 76 introduced in Round 1 and 59 added across Rounds 2 and 3. Statements are detailed with percentage agreements in an additional data file [Additional File 2]. Four core domains were explored:
‘who and when’ (28 statements) - which young people should be asked by practitioners about their online activities, how frequently, and in what circumstances?
‘how’ (30 statements) - most appropriate ways of starting and conducting conversations about online activities to maximise engagement and minimise blame or stigma;
‘what’ (61 statements) - what should be covered within conversations about online activity to enable practitioners to identify risk and support a young person’s mental health?;
‘outcomes’ (16 statements) - what should be done with the information from conversations, particularly where risky use is uncovered?.
The number of statements accepted, rejected, or without consensus by domain, round and panel are tabulated in an additional data file with commentary describing patterns across panels [Additional file 3]. There was strong overlap across panels, although the PP reached consensus on a greater number of items and were more likely to reject items than the YPP. The most contentious domain was ‘who and when’—the PP favouring a more inclusive approach, while members of the YPP expressed concerns about possible iatrogenic risks of discussing online content with some young people. Disagreements and uncertainties are detailed below.
Good practice indicators
Ninety-six statements were agreed by consensus in both panels and progressed for possible inclusion (Fig. 1).
These were organised into 27 Good Practice Indicators (GPIs) (Table 2).
It was agreed practitioners should ask all young people about their online activities (PP 95%, Round 1; YP 85%, Round 3); that this should happen at their first meeting (for instance, when taking a history or assessing risk) and should not be a ‘one-off’ conversation but take place regularly, as required. Agreed ‘red flags’ indicating a conversation may be particularly helpful to pursue focused on the presence of specific or changing patterns of device use (e.g. increase in notifications), presenting problems (e.g. bullying) or symptoms (e.g. sleep disturbance or suicidal thoughts) (Table 3).
Panels agreed such conversations should be: introduced spontaneously as part of the flow of conversation; open-ended and fluid rather than a tick-box assessment; contextualised with an explanation from the practitioner about why they are asking (for instance, by referencing possible risks); and that practitioners should approach conversations as a learner, being curious and prepared to ask questions to enhance their understanding of young people’s interactions with the online world. Further, to facilitate conversations, clinicians should have an up-to-date knowledge of the online world and be able to use up-to-date language. High levels of consensus (> 90%) were reached around practitioners explicitly addressing the young person’s potential fear of judgement and limits to confidentiality; providing opportunities to disclose without parents being present; normalising online activity and its discussion; and acknowledging that being online may also benefit mental health.
Topics that ‘should always be covered’ when discussing online activities were agreed, with tailored lists for patients presenting with disordered eating, self-harm or suicidal thoughts (Table 4). Where worrying online activity is uncovered, panels endorsed extending conversations to ask for the names of sites visited, descriptions of content created by the young person and details of participation in online groups. There was strong consensus (> 90%) that practitioners should also initiate reflective discussion, encouraging the young person to explore issues such as the thought processes and triggers underlying their online activities and the resulting impacts (Table 5). The statement that ‘practitioners should encourage young people to reflect on how they may cause harm to others online’ was introduced from YPP free-text and subsequently received 100% endorsement from this panel (PP, 79%), indicating this as a priority issue for young people.
With respect to outcomes, both panels agreed concerning activity should be flagged in clinical notes (PP 100%, YPP 90%) and that strategies for addressing online safety should be incorporated when writing personalised treatment or safety plans as detailed in Table 6 (consensus on items ranging from 75–100%). Panels agreed practitioners should encourage young people to actively manage their own online safety (PP 100%, YPP 90%) and support positive engagement with the online world instead of suggesting bans (PP 89%, YPP 95%), though local safeguarding procedures should be followed where indicated. Where recommending apps, panels expressed a need for clinicians to support their recommendations by presenting a choice of apps, offering to demonstrate how they work and following-up on use in subsequent appointments to explore effectiveness.
Excluded statements: ‘conflicts’ and ‘near-misses’
Thirty-nine statements were excluded. These represented unclear opinion (n = 21), conflicts (consensus in one panel, other panel expressing opposing trend) (n = 4), or ‘near-miss’ statements (one panel reaching consensus, the second expressing trend in the same direction) (n = 14). There were no instances where both panels rejected (disagreed by consensus) the same statement, and thus no negative items for inclusion in the GPIs.
Conflicts surrounded if ‘it is acceptable for any clinician to ask about online activities’ (PP 95% agree, YPP 50% disagree); and if ‘it is inappropriate to ask young people who are acutely very unwell’ (low conflict, PP 53% disagree; YPP 81% agree), or ‘experiencing paranoia’ (mid conflict; PP 80% disagree, YPP 60% agree). Involvement of parents was another area of contention: 87% of clinicians thought parents should be involved where the young person is aged 12–15, while YPP opinion was split. Finally, the YPP largely disagreed with the statement ‘young people should be asked about online activities at every consultation’ (81% disagreement) while the PP were undecided (20% agree, 47% disagree).
There were 8 ‘near-miss agree’ and 6 ‘near-miss disagree’ statements (Table 7). Three referred to clinician knowledge (discussed below but not included within the GPIs). Near-miss agree items indicated other possible topics (‘what’) to cover within conversations: details of online conversations where worrying use is apparent (low agreement); viewing and posting images of bodies (medium agreement) and influencers followed (medium agreement) for patients with disordered eating; and online purchasing of items associated with harm (means) for patients with self-harm/ suicidal feelings (medium agreement). Near-miss disagree statements contributed to debate around the inappropriateness of asking some young people about their online activities, revealing a majority view that practitioners should not avoid asking those who are actively suicidal (PP 93%, YPP 56%), or under 10 years (100% PP, 56% YPP), and that it is acceptable for practitioners to ask about online activities where not raised by the young person (95% PP, 56% YPP). The use of pre-set questions was commonly rejected (75% PP, 58% YPP).
Open-ended questions provided insight into key areas of discord and suggestions about how some GPIs could be operationalised in practice.
‘Who’: which clinicians should ask?
Half of the YPP thought asking about online activities should only take place within the context of a trusting, on-going relationship where good rapport had already been established. They warned that if any clinician asks, this could result in a young person being asked multiple times and might exacerbate feelings of judgement, invasion of privacy, and resentment at an inappropriate level of blame being focused on online activities where other factors may be more pertinent. The PP acknowledged that an established relationship was desirable but did not regard this as a prerequisite. Their overriding perspective was that discussing online activity is important to assessment and safeguarding, so is “everyone’s responsibility” and should be addressed where possible, including in A&E:
Given online activities can be harmful and expose young people to various risks, I think it should be acceptable for any [clinician] to ask. You never know, you might be the first person to raise it. (PP)
There may be clinicians or settings that it would be more appropriate, e.g. an ongoing relationship… However, opportunities to explore this should not be wasted – if a young person… is only likely to be meeting with clinicians on a short-term or one-off basis, the opportunity to discuss online activity should be used. (PP)
‘Who’: which young people—risk of asking
Members of the YPP discussed the potential inappropriateness of practitioners asking high-risk or reluctant young patients about their online use, voicing concerns that this could exacerbate symptoms, provoke distress or resentment, or lead the unexposed to harmful content:
If a person is paranoid then they may get more paranoid if asked about their online activity. (YPP)
[It is inappropriate to ask] when they are clearly hesitant and reserved about sharing. It may be a trigger for them, so the subject should be broached carefully, and perhaps only when the young person brings it up in their own time. (YPP)
Being introduced to the idea of using online activities in different ways could lead to more young people discovering new methods of self-sabotage. (YPP)
Some flagged such risk could be particularly pertinent for patients with presenting problems where issues of illness identity and competition can be relevant:
In terms of specifically eating disorders, where there is a high rate of competition to be the ‘most unwell’, giving [online] suggestions… is an indicator that that’s what other ‘anorexics’ do, therefore this is something they should be doing (YPP).
While a few practitioners acknowledged possible risk and that occasionally there could be “better times” to ask (for example, if a patient was acutely psychotic and needed stabilising), the general view was that avoidance could pose greater risk, so asking should not be ruled out for any particular situation. Some YPP members also presented these arguments.
A number of the scenarios described [in Delphi statements] potentially increase risk when coupled with online activity of certain kinds (e.g. suicidality) and so it would be pertinent to ensure this is accounted for within assessment (PP)
Online activity can often provide a window into what is going on for the young person, therefore avoiding it is neglecting information (PP)
Practitioners argued that risk can be mitigated by method of asking. Specifically, by a broad approach of “curious questioning as opposed to explicitly listing harmful resources” and being led by the young person’s answers to avoid suggestion. For instance:
I will avoid asking about use of specific sites or tags because I don’t want to introduce new sources of inspiration. But that wouldn’t stop me from asking about their experience and what sites they visit/ what searches they use. (PP)
Members of the YPP agreed a way forward was to invite young people to talk about what they had encountered rather than asking if they had accessed specific content. Careful consideration of the ‘how’ and ‘what’ domains was therefore seen to override concerns about ‘who’ or ‘when’.
‘How’: Normalising online activities.
To support the GPI that practitioners should normalise online activities when discussing these, participants were asked for examples of how this could be done. Common ideas are summarised in Table 8, though tensions arose with respect to how a practitioner should position themselves. For example, opinion was divided about whether practitioners should attempt to use online slang. Also, while one practitioner drew on a recurring theme about the need to “show curiosity and interest to learn”, a YPP member warned that clinicians should “not appear to be fascinated” if normalisation is to be achieved, revealing a possible tension in how this could be interpreted.
‘What’: Adapting conversations based on personal characteristics
It was noted that simplistic language is likely to be more appropriate for younger patients and some suggested the questions asked should take account of typical content accessed by particular age groups, such as popular apps, games or platforms. A recurring YPP concern was a potential to “adversely influence” younger children by leading them to harmful content if asking about some topics (e.g. pornography):
Younger people may not yet be exposed to some topics and become curious after being questioned. Filter questions. (YPP)
However, the danger of limiting discussion due to incorrect assumptions and thereby missing risky use was raised by both panels as a challenge to navigate.
I don’t think we should make assumptions about what we expect a young person’s online activity to look like. It is better to remain curious and ask everyone the same questions even if we think they may not be relevant. (PP)
Uncertainty about adapting conversations for ethnicity, gender or sexuality related to the same concern, although the YPP noted clinicians should be aware marginalised youth may experience more online hate or be more susceptible to grooming as they may more frequently look to online spaces to find relationships due to difficulties building these offline. Ideas about how to adapt for disability focused on neurodevelopmental disorders but were unclear beyond basic suggestions about accessible language.
Outcomes: supporting safe and positive use
To realise GPI aspirations around outcome, panels were asked for specific ideas about how practitioners can empower young people to engage positively with the online world and to suggest strategies for responding to harmful content. The YPP drew on strategies they use and find useful, while the PP shared examples of strategies they currently recommend. There was strong overlap between the responses yielded (Table 8). Participants noted these strategies are needed in combination and that facilitating insight and ability to self-monitor is fundamental to enabling young people to assert agency. For instance, prompting self-awareness of triggering content or influencers and identification of positive alternatives is a pre-requisite for commitment to behavioural strategies around blocking or unfollowing.
The YPP gave specific examples of how a practitioner could apply such strategies to address with young people the harm they could cause others online. These included: use of reflective, non-judgemental discussion to increase self-awareness about how images and other content posted by the young person may be perceived by others; advice to use tactics such as making accounts private or refraining from using hashtags in order to protect others; and recommending use of pen and paper as an alternative outlet for strong negative feelings.
Outcomes: involving parents/ guardians
Young people were reluctant for parents to be involved in conversations about online activity, stemming from a perception they may misunderstand online behaviour or take an “over-exaggerated” view leading to counterproductive actions (blocking, banning) and “unwarranted worry or tension” in the household. Some YPP members raised privacy, noting many young people prefer to conceal their online lives from parents and involving parents may lead to young people feeling “ganged up on” and practitioner-patient trust being eroded. A few practitioners similarly cautioned that involving parents should not occur without being mindful of parents’ possible misperceptions about the online world:
Some parents get very angry and alarmed…there may need to be a general conversation first with parents to assess feelings and reactions. (PP)
Practitioners however offered several ways parents could be involved in discussions where patients are under 16 years. These ranged from educating parents in general terms about the online world, to making them aware of their child’s specific online activities and included: discussing ways to support safe use, such as imposing boundaries on screen time and using parental controls; and fostering open dialogue with their child, particular around unhelpful online interactions. Some YPP members concurred that parents could be given general information about online risks and advice about supporting a young person who is “an excessive user” or “upset online” without imposing “blanket bans”. Panels stated parental involvement should be contingent upon the young person’s consent, evidence of risk, or safeguarding issues. The same ideas were expressed where the young person is over 16 years, though with greater emphasis from both panels on the young person maintaining control and there being a higher threshold of risk.
Practitioner knowledge and support needs
Views on practitioners training and support needs were also explored following consensus that practitioners should display up-to-date language and knowledge. This was seen as essential for reassuring young people to disclose and ensuring conversations are useful. Qualitative data suggested this meant being ‘broadly familiar’ with the main social media platforms and how these function, potentially harmful mental health-related online communities, helpful sites, apps and safety features including time limiters and privacy settings, and basic online slang and text speak. Practitioners perceived a particular need to be updated about new trends given the rapidity with which the online world evolves but young people asserted that practitioners should receive more foundational training to instil appreciation of the place of the online world within a young person’s life and aid recognition of what is ‘normal’ and when to pathologize. Notably, all participants from both panels agreed that young people should play a key role in training clinicians.
Using a mixed-methods Delphi approach, we sought the expertise of mental health practitioners and young people with lived experience of mental health difficulties to develop good practice indicators (GPIs) around how to conduct conversations with young people about their online activities. This resulted in 27 indicators across four domains, generated from statements reaching a consensus agreement of 75% or more in both panels. These covered: i) ‘who’ and ‘when’ to ask; ii) ‘how’ conversations should be conducted; iii) ‘what’ should be discussed; and iv) ‘outcome’—how conversations should be taken forward.
There was consensus that all young people should be asked about their online activities, this should occur at first meeting and then at regular intervals, and that there are red flags indicating times where a conversation may be particularly indicated. A fluid approach was emphasised, with open-ended prompts embedded spontaneously within the flow of conversation. The importance of providing context and reassurance, normalising both online activity and discussion of this, and acknowledging positive aspects of online use to ensure a non-judgemental exchange were also highlighted. Key topics to always address were delineated, with additional topics to ask patients with disordered eating or self-harm behaviours, and follow-on areas for gaining more specific information about worrying activity. There was strong agreement that asking about online activity should move beyond information gathering to take the form of a deeper conversation with a focus on encouraging the individual to reflect on the meanings and impact of their online behaviour. It was agreed the primary objective should be to empowering young people with insight and strategies to actively manage their online safety and derive positive benefits, rather than on ‘stopping’ online activity. It was also agreed that concerning online activity should be flagged in clinical records and followed up, and that personalised strategies for on online safety should feature within treatment plans. Qualitative data suggested methods for normalising discussion of online activities and for supporting positive online behaviour.
Areas of conflict and uncertainty between panels surrounded possible risks of initiating conversations about online harms and whether practitioners should involve parents in discussions. Young people tended to recommend a more cautious approach, expressing concerns about the potential to exacerbate symptoms or flag the existence of risky online content if raising online activity with the very ill or very young. However, practitioners suggested the risks of not enquiring may be greater and that concern could be mitigated by method of asking. In accordance with principles of good clinical care, both panels stated parental involvement should be contingent upon the young person’s consent and/ or sufficient safeguarding concern. This was reflected by the GPIs that there should be explicit discussion around confidentiality and that all young people should have the opportunity to discuss online activity without parents being present. Involvement of parents for those under 12 was agreed within this context and implies conversation about online activity with general advice for this age group, not that confidentiality should be broken. Young people however were notably reluctant to endorse parental involvement for those over 12 years and set a high threshold of risk to be present before confidentiality should be overridden. Both panels implied parental education around online harms may be needed to ensure that involving them is supportive and productive.
The relevance of digital technology to young people’s mental health is indisputable, having been described as ‘infrastructural’ to their everyday life , and recognised as both as a positive and negative force. It has been suggested that practitioners address this during consultations  and that asking about online use could facilitate risk assessment . However, to date, guidance and training about how to conduct and focus such conversations has been lacking . Our good practice indicators fill this gap, offering some clarity on how practitioners might work with young people to improve online safety. While not contradicting earlier suggestions, our findings urge caution about practitioner reliance on promoting use reduction or parental involvement . Our findings focus primarily on a need for open, non-judgemental exchange and aiming to increase young people’s autonomy around their online behaviour. This is in line with other evidence about the most effective consulting contexts for improving communication with adolescents  and available evidence about best approaches for reducing online risk . Our findings also highlight a role in assisting young people to capitalise on positive aspects of the online world in relation to mental health, emphasised by some commentators. Previously expressed practitioner concern that asking about online behaviour could create risk  re-emerged in our young people panel but was disputed by practitioners.
Strengths and limitations
The involvement of two panels – young people and practitioners—and use of an iterative approach underpinned by qualitative enquiry, afforded creation of a refined set of GPIs, responsive to the priorities and experiences of the major stakeholders and thus likely to have good acceptability. These are supported by a narrative providing additional nuance around some issues and including suggestions about how general statements may be operationalised in practice. To our knowledge, this is the first guidance in this area.
All panel members had relevant expertise and the study sample size, retention rate and consensus cut-points were within recommended ranges for robust Delphi methods . The two panels were balanced, giving equal weight to each perspective. Our young people panel was diverse with respect to age and diagnosis. Similarly, a range of practitioners was involved with respect to clinical experience and role. However, there were limitations to inclusivity, which should be explored in further research. Males were substantially underrepresented in both panels and ethnicity and socioeconomic status were not recorded. All panel members were based in England or Wales. Our panel did not include children under 13 years, limiting our ability to reach conclusions about application for the youngest age groups. Further, inclusion of social care practitioners, may have added an additional perspective on safeguarding.
Some topics, such as young people’s use of online pornography and online gambling, were not included in the GPIs despite indication that these online activities are relevant to young people’s mental wellbeing [20, 21]. Such activities are patterned by characteristics including sex and the underrepresentation of male participants in our panel may have led to an underestimation of importance. A more diverse panel may have provided further clarification around discussion of such topics and their exclusion from the GPI topics to always ask about should not preclude discussion or detract from practitioners’ awareness of their relevance. Similarly, findings were less clear around personalisation of conversations for population groups, such as those with neurodevelopmental disorders, despite a sense that this was important. This may be because our panels lacked lived-experience in these areas. Finally, inclusion of a parent/ carer panel would have been informative, as highlighted by contention over when and how to involve parents in conversations. This is an area for further research.
This study provides much needed preliminary good practice indicators for mental health practitioners about how to engage young people in conversations about their online activities and respond to the issues raised. Unlike traditional approaches to online harms, which have tended to focus on restriction, findings from this study promote the idea of practitioners facilitating awareness and empowering young people to exercise agency in relation to their online behaviours and safety.
Pilot work is required to examine use of the GPIs in practice. As well as considering their transferability to settings such as primary care, and to particular population groups, this should focus on examining feasibility in the context of clinical constraints relating to time and resources. It should be recognised that it may not be achievable to cover all GPIs in an initial assessment and that discussion may span subsequent sessions. The conversations proposed may be more suited to long-term clinical relationships. Further research may be able to derive a refined list of key content for initial or one-off encounters. Evaluation should also include an attempt to measure patient outcomes arising from the opportunity to address online behaviour with a practitioner and investigate which of the suggested practitioner responses appear most beneficial. Other useful next steps may include co-design of strategies and tools that may be used in crisis planning and in brief interventions to facilitate empowerment and positive use. Additionally, findings have identified potential training needs for practitioners, though this presents challenges. Consideration is required of how these are best met, where this can be focused on general principles, and the extent to which knowledge of up-to-date trends and terminology is attainable given the rapidly evolving online terrain. Education of parents/ carers may also be required if they are to be included within conversations.
Availability of data and materials
The quantitative dataset supporting the conclusions of this article are included within the article and its additional files. The qualitative dataset used and analysed during the current study are available from the corresponding author on reasonable request.
Good practice indicator
Young people panel
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We extend thanks to Esther Kissane-Webb for administrative support and to all panel members including (but not exclusively) the following contributors who opted to be named. Young people panel: Livi Morgan-Finn, Jasmine Ashraff, Louise Chandler, Issy Buchan, Issy Hatton-Williams, Rebecca Woolford, Libby David, Nusaybah Choudhury, Charlotte Storey, Ben Lamont, Emma Robinson, Shivani Baghirathan Nicholls. Practitioner panel: Rebecca Male, Julie Alderson, Melanie Merricks, Laura Cox, Jodie Rawlings, Ann Hughes, Lucy Harris, Megan Simmonds, Emma Lawson, Clair Henry, Ben McLewis.
This work was supported by the Medical Research Council (MRC), Arts and Humanities Research Council (AHRC) and Economic and Social Research Council (ESRC) as part of the Adolescence, Mental Health and the Developing Mind joint funding programme under grant MR/T046716/1. The funder played no role in study design, collection or interpretation of data, or preparation of the manuscript.
Ethical approval and consent to participate
Ethical approval was obtained from the University of Bristol’s Faculty of Health Sciences Research Ethics Committee (ref: 108566, 12/11/20). The study was conducted in accordance with the relevant guidelines and regulations for medical research involving human subjects. Informed consent was obtained from all subjects/ participants and their parents/ legal guardians where the participant/ subject was aged 16 years or under.
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The authors declare no competing interests.
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Additional file 1.
Engagement research and questionnaire development. Describes methods used to generate the round 1 Delphi questionnaire and the underlying basis for the content.
Additional file 2.
Full quantitative data set for Delphi study investigating how Mental Health Practitioners should converse with young people about online activities. All statements are detailed in full, showing round introduced and percentage agreement in each panel and across rounds (Tables S1-S4).
Additional file 3.
Statements accepted, rejected and without consensus by domain, round and panel for Delphi study investigating how Mental Health Practitioners should converse with young people about online activities. The number of statements reaching consensus or being rejected in each round are summarised (Table S5) and the patterns, similarities and differences across panels are discussed.
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Biddle, L., Rifkin-Zybutz, R., Derges, J. et al. Developing good practice indicators to assist mental health practitioners to converse with young people about their online activities and impact on mental health: a two-panel mixed-methods Delphi study. BMC Psychiatry 22, 485 (2022). https://doi.org/10.1186/s12888-022-04093-w
- Young people
- Mental disorder
- Social media