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Drawing on insights from Telehealth trial for COPD, and the rise in wearable technology for self monitoring. Presented at Health 2.0 meetup, London April 2014
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actually increase engagement
@alextarling
does giving patients more data
& improve outcomes?
user experience research is about:
actually increase engagementdoes giving patients more data
& improve outcomes?
perceptions
emotionsbehaviour
s
beliefs
the Lothian COPD telehealth trial
the telehealth context of care
$10,000$1,000$100$10$1
Qualityof Life
Cost of Care / Day
Independent, Healthy Living
Community Clinic
Chronic DiseaseManagement
Doctor’s Office
Home Care
Assisted Living
Skilled Nursing Facility
Residential Care
Specialty Clinic
Community Hospital
Emergency Department
Acute Care
ICU
patients completed daily ‘health sessions’:• daily symptom questionnaire with 8
questions:– “I am more breathless than usual”– “My sputum has increased in colour”– “My sputum has increased in
amount”, etc– Answers are scored, scores above
certain threshold trigger a clinical response
• physiological measures on a daily/weekly basis or as needed:– Pulse Oximeter (Pulse, SpO2), Peak
Flow Meter (FEV1), Weight Scales.
Community Respiratory Physiotherapy team
the service model
Patient and carers at home
When alerted: physiotherapy team contacts patient by videoconference or home visit
Patient’s daily readings and symptom scores uploaded
Daily monitoring by Community Respiratory Team
remote monitoring vs. self care
• service designed as remote monitoring with patients playing a passive role as providers of data not consumers
– “As the doctor says: ‘You don’t have to tell us, we’ll tell you, we’ll phone you and tell you that your oxygen levels are down or whatever, and then there’ll be a prescription’” (spouse of patient)
– “It made me more assured. In a way it was a relief, thinking that should I ignore my own thoughts on getting a doctor or something like that, this organisation would get hold of a doctor if their readings showed I needed a doctor” (patient)
• apparent paradox in this service model...
– strategy for chronic conditions is to increase self-care – the model increases professional surveillance of the patient– clinician concerns over increasing dependency on healthcare service
1. participating in daily care plans as a regular, intentional, socially-connected activity for patients.
2. increased awareness of personal health status, awareness of significance of changes.
3. engagement and ownership: patients assuming a direct role in owning, interpreting and managing access to their own health data.
despite this focus on remote monitoring, we saw examples of ‘emergent’ self-care and enhanced disease awareness:
actually increase engagementdoes giving patients more data
& improve outcomes?
behaviours
emotionsbeliefs
perceptions
actually increase engagementdoes giving patients more data
& improve outcomes?
behaviours
emotionsbeliefs
perceptions
... in order to evoke an emotionally resonant response
data needs to elicit personal meaning..
System One
95%
5%
SubconsciousEmotionalHotInstinctsDoing“I love stories”Makes decisions
System TwoConsciousRationalCold/CoolPlanningThinking“I love numbers”Justifies decisions
@DeniseHampson
actually increase engagementdoes giving patients more data
& improve outcomes?
behaviours
emotionsbeliefs
perceptions
... in order to evoke an emotionally resonant response
data needs to elicit personal meaning..
Consumer fitness and wellness self-monitoring:
actually increase engagementdoes giving patients more data
& improve outcomes?
behaviours
emotionsbeliefs
perceptions
... in order to evoke an emotionally resonant response
data needs to elicit personal meaning..
.. which has the potential to drive intentional, goal oriented action
actually increase engagementdoes giving patients more data
& improve outcomes?
...no (however...)
they have an emotional engagement
when patients develop meaningful interpretations of their personal health data
which creates the potential for positive changes to beliefs and behaviours
@alextarling