Concerns about trust, security & safety in mhealth: are they justified, and what to do about them?



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Concerns about trust, security & safety in mhealth: are they justified, and what to do about them? Jeremy Wyatt DM FRCP ACMI Fellow, Clinical Adviser on New Technologies Leadership chair in ehealth research, University of Leeds From 1/1/16: Director, Wessex Institute of Health, University of Southampton

Agenda Why bother with mhealth? Why do mhealth trust, security and safety matter? What is the evidence about these? What to do to alleviate these problems? Conclusions

Why bother with mhealth? 1. Face-to-face contacts do not scale 2. Smart phone hardware used by 65%+ of adults: Cheap, convenient, fashionable Inbuilt sensors / wearables allow easy measurements Multiple communication channels: SMS, voice, video, apps 3. mhealth software enables: Unobtrusive alerts to record data, take action Incorporation of Susan Michie s behaviour change techniques (eg. present in 96% of drug adherence apps) Tailoring, which makes behaviour change more effective (d=0.16, Lustria, J H Comm 2013)

Cost in per encounter Why digital channels? 10 9 Mean UK public sector cost per completed encounter across 120 councils 8,60 Source: Cabinet Office Digital efficiency report, 2013 8 7 6 5 5,00 4 3 2,83 2 1 0 0,15 Face to face Letter Telephone Digital

Trust, security and safety Public space mhealth that is fun to use mhealth that is functional Recommendations from friends People use mhealth People trust mhealth Professional space Evidence of safety Professionals recommend mhealth Professionals trust mhealth Evidence of effectiveness Evidence of data security

First Folio As You Like It Public Domain Photo taken by Cowardly Lion - Folio Society edition of 1996 Privacy and mhealth apps Permissions requested: use accounts, modify USB, read phone ID, find files, full net access, view connections Our study of 80 apps: average of 4 clear privacy breaches for health apps, only 1 for medical apps We know that - we read the Terms & Conditions! (this one only 1200 words, but many much longer ) With Hannah Panayiotou & Anam Noel, Leeds medical students

Recent evidence on privacy & mhealth apps Huckvale et al 2015 study of 79 accredited lifestyle apps from NHS Apps library: Only 53 (67%) had a privacy policy: policies vague, did not explain types of data being shared No app encrypted data held on the device 70 (89%) leaked confidential data over network 35 included identifiers, 23 sent IDs without encryption 4 apps sent both IDs and health information without encryption

App price US dollars Are apps based on sound evidence? 45 Price ($US) of 47 smoking cessation apps versus evidence score (data from Abroms et al 2013) 40 35 y = 3.7-0.1x R² = 0.016 30 25 20 15 10 5 0 0 5 10 15 20 25 30 35 Evidence score: high score means app adheres to US Preventive Service Task Force guidelines

Current evidence on app safety Apps for insulin dosage adjustment (n= 46, Huckvale 2015): 14 (30%) declared source of algorithm, 3 (9%) validated input data, 27 (59%) allowed calculation with missing data 17 (37%) did not update when input data was changed Only 1 app was free of issue s Asthma apps (Huckvale 2015): Number doubled from 93 in 2011 to 191 in 2013 23 (25%) of the first group of 93 withdrawn; 147 new apps in 2 years Newer apps not more likely to include EB advice: only 75 (50%) of 147 gave basic info on asthma, 36 (24%) had diary functions Only 4 (17%) of 23 apps advising on asthma management were consistent with guidelines CVD risk apps

Overall results Located 21 apps, only 19 (7 paid) gave figures All 19 communicated risk using percentages (cf. advice from Gigerenzer, BMJ 2004) One app said see your GP every time; none of the rest gave advice Some apps refused to accept key data, eg. age > 74, diabetes Heart Health App

Misclassification rate Misclassification rates Rates varied from 7% (safe?) to 33% (unsafe!) Of 19 apps, 8 (42%) misclassified at least 20% of the scenarios Median error rate free 13%, paid 27% (p = 0.026) 35% 30% 25% 20% 15% App misclassification rate (20% threshold; paid = dark blue) 10% 5% 0%

Scoping review on app effectiveness 21 trials of apps used by patients / the public: 3 studies were confounded (used app + much else besides) 3 were equivalence studies (does app save resources, but with same outcomes?): 2 were positive Of the remaining 15 trials*: 8 studied health behaviours: 7 positive, 1 worse (compared to SMS for smoking cessation) 5 studied clinical process: 3 positive, 2 equal 5 studied patient outcomes: 3 positive, 2 equal Overall (inc. equiv. trials): 15 positive, 4 equal, 1 worse * 3 measured more than one of these Source: JW work in progress to date

Possible quality approval processes to improve mhealth Methods Advantages Disadvantages Examples Wisdom of the crowd Users apply quality criteria Classic peer reviewed article Physician peer review Developer selfcertification Simple user ranking Explicit Rigorous (?) Timely Dynamic Dynamic Hard for users to assess quality; click factory bias Requires widespread dissemination; can everyone apply them? Slow, resource intensive, doesn t fit App model Not as rigorous Scalable? Requires developers to understand & comply; checklist must fit apps Developer support Resource light Technical knowledge needed Multitude of developers CE marking, external regulation Credible Slow, expensive, apps don t fit national model Current app stores MyHealthApps RCP checklist 47 PubMed articles imedicalapps, MedicalAppJournal HON Code? RCP checklist BSI PAS 277 NHS App Store, FDA, MHRA

User ratings: app display rank versus adherence to evidence Study of 47 smoking cessation apps (Abroms, 2013)

Regulation of medical apps by FDA, FCC If classified as a medical device by FDA a product must demonstrate efficacy, but: Only 100 apps so far classified as a medical device Decision to exercise enforcement discretion on most medical apps So, FDA has not actually banned any apps, yet However, the Federal Communication Commission has banned some apps with misleading claims, eg. Acne Cure (no evidence of claimed benefit of iphone screen backlight) Sharpe, New England Center for Investigative Reporting, Many health apps are based on flimsy science at best, and often do not work. Washington Post, November 12th 2012

We need to think differently Old think Paternalism: we know & determine what is best for users Regulation will eliminate harmful Apps after release The NHS must control Apps, apply rules and safety checks App developers are in control Quality is best achieved by laws and regulations The aim of Apps is innovation (sometimes above other considerations) An Apps market driven by viral campaigns, unfounded claims of benefit New Think Self determination: users decide what is best for them Prevent bad Apps - help App developers understand safety & quality Self regulation by developer community Consumer choice informed by truth in labelling Aristotle s civil society* is in control Quality is best achieved by consensus and culture change App innovation must balance benefits and risks An Apps market driven by fitness for purpose (ISO) & evidence of benefit The elements that make up a democratic society, such as freedom of speech, an independent judiciary, collaborating for common wellbeing

Our quality criteria for apps, based on Donabedian 1966 Structure = the app development team, the evidence base, use of an appropriate behaviour change model etc. Processes = app functions: usability, accuracy etc. Outcomes = app impacts on user knowledge & self efficacy, user behaviours, resource usage Wyatt JC, et al. Clinical Medicine December 2015

Labelling of apps Analogy: legally required food labels listing ingredients, allergens etc. Q: What fields for a health app label? A: Sponsor; intended user; privacy policy; source of content; results of accuracy and impact studies?

Some criteria for an mhealth quality approval process 1. Empower patient & professional choice 2. Promote survival of the fittest and a proper market, not just innovation for its own sake 3. Use criteria that make sense to patients / professionals / health systems / industry 4. Scalable to thousands of apps 5. Proportionate to clinical risk 6. Resistant to manipulation, and auditable

Conclusions 1. The quality of mhealth tools varies too much 2. User rating, professional reviews, developer selfcertification and regulation are not enough 3. To help reduce apptimism and strengthen other methods, we need to agree quality criteria, evaluate apps against them and label each app with results 4. This will support patients, health professionals, health systems and app developers to maximise the benefits of mhealth Contact me: j.c.wyatt@leeds.ac.uk