professional standards authority conference – 28 march 2014 regulatory design: the role of...

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Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran Walshe and Denham Phipps University of Manchester, UK [email protected]

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Page 1: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran

Professional Standards Authority conference – 28 March 2014

Regulatory design: the role of programme theory in evaluating healthcare regulation

Kieran Walshe and Denham Phipps

University of Manchester, UK

[email protected]

Page 2: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran

• Programme theory in evaluation research

• Applying programme theory to understanding the Care Quality Commission’s regulatory model

• Conclusions and reflections

Page 3: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran

Programme theory

• “A plausible and sensible model of how a programme is supposed to work” which “provides the hypothesized links between program features and planned outcomes to be tested” (Bickman 1996)

• Derived from existing knowledge/research and from programme actors – policymakers, leaders etc

• Makes programme design choices explicit/visible and open to contestation/adjudication

• In “what works” – helps distinguish between theory and implementation, to understand mechanism and context, and to generalise

Page 4: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran
Page 5: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran

CQC study objectives and methods

• Develop a “logic model” to map programme theories underlying the regulatory model

• Use it to develop a framework for identifying and prioritising topics and questions for evaluation

• Document review – mainly CQC publications/reports

• Interviews with circa 20 CQC staff in London and Preston

• Review of the research literature and comparison of practice with four other regulators (two in health elsewhere, two in other settings in UK)

Page 6: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran

Regulatory model: components

• Registration

• Compliance

– Standard setting

– Information gathering and risk assessment

– Inspection and reporting

• Enforcement

• Information provision

Page 7: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran

Registration

• Three main models of registration:

– Threshold – tool for driving improvement, deterring poor providers from registering, leverage, assurance

– Relationship – get to know provider, build knowledge base, establish relations, triage or risk assess

– Administrative process – collect basic data, register and then pass on to others to regulate

• Consequences – foregone opportunities, deferred regulatory load

Page 8: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran

Compliance: standard setting

• Four main models of standard setting:

– Mechanism to frame/set stakeholder expectations

– Mechanism for improvement through self-enforced compliance

– Mechanism for compliance through measurement and enforcement

– Mechanism for differentiating performance of providers

• Consequences: generic standards, minimal/median /maximal level, content and focus, understanding and implementation

Page 9: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran

Compliance: information gathering and risk assessment

• Three main models of proportionate regulation:

– Using information to determine when to use regulatory interventions

– Using information to focus/direct the content of regulatory interventions

– Letting providers know about likely regulatory intervention

• Consequences: timely, meaningful, predictive information and intelligence, capacity to use/interpret it

Page 10: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran

Compliance: inspection

• Four main models of inspection:

– Driver for improvement in advance of inspection

– Measure of compliance to support enforcement

– Measure of performance to support improvement

– Driver for other providers to improve

• Consequences: direct observation and proxy measures, reliability and validity of judgements, inspection workforce competence

Page 11: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran

Enforcement

• Four main models of enforcement:

– Informal enforcement or prospect of enforcement

– Incentive to drive compliance

– Symbolic action to drive compliance

– Driver for other organisations to achieve compliance

• Consequences: resource to enforce, scale of penalty, effects of frequency, spillover effects, capacity to change

Page 12: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran

Information provision

• Three main models of information provision:

– Information to be used by other stakeholders in their decision making

– Information to be used by providers in compliance and improvement

– Information as a mechanism for public accountability

• Consequences: limited volume, utility and timeliness of data, usability by stakeholders

Page 13: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran
Page 14: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran

Summary of current regulatory model

• Registration as an administrative process

• Compliance

– Standard setting to measure compliance and support enforcement

– Information gathering and risk assessment to inform or direct regulatory intervention

– Inspection and reporting to measure compliance

• Enforcement as an incentive for compliance

• Information provision to support decision making and accountability

Page 15: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran

Current regulatory model: key issues

• Consistent with a mission as a “safety-net” regulator focused mainly/only on compliance at the bottom of the performance distribution

• Some problems even so with the model

– Regulatory standards - measurability and meaning

– Attempts proportionate regulation without predictive information and capacity to use it

– Inspection process – reach and workforce competence

– Information provision – little useful information to share

Page 16: Professional Standards Authority conference – 28 March 2014 Regulatory design: the role of programme theory in evaluating healthcare regulation Kieran

Conclusions and reflections

• For CQC – a contribution towards their rethinking of their regulatory strategy/philosophy and model

• Programme theory evaluation – most useful (and most difficult) when theory(ies) in use unclear, ambiguous, complex/complicated

• Place for programme theory in regulatory design – not just post hoc evaluation

• Wider question of how best to integrate evaluation into regulatory innovation/policy development/practice