ASPIRE 2: Action to Support Practices Implementing Research Evidence

Conditions

Topic: Diabetes, Primary Care

Robbie Foy, Thomas A. Willis, Liz Glidewell, Rosemary McEachan, Rebecca Lawton et al. (31 authors)

Programme Grants for Applied Research2020-03-0115 citations

An adaptable implementation package targeting evidence-based indicators in primary care: A pragmatic cluster-randomised evaluation

Thomas A. Willis, Michelle Collinson, Liz Glidewell, Amanda Farrin, Michael Holland et al. (15 authors)

PLoS Medicine2020-02-2838 citations

10.1371/journal.pmed.1003045

Action to Support Practices Implement Research Evidence (ASPIRE): protocol for a cluster-randomised evaluation of adaptable implementation packages targeting ‘high impact’ clinical practice recommendations in general practice

Thomas A. Willis, Suzanne Hartley, Liz Glidewell, Amanda Farrin, Rebecca Lawton et al. (18 authors)

Implementation Science2015-12-0119 citations

10.1186/s13012-016-0387-5

Interventions

1. Audit and Feedback: This will be by practice and will be repeated regularly during the trial. It will include comparisons with other (anonymised) practices, information to illustrate benefits of ch

Eligibility

Inclusion criteria

Inclusion criteria: General practices within the ten Clinical Commissioning Groups (CCGs) in West Yorkshire (Airedale Wharfedale and Craven CCG, Bradford City CCG, Bradford Districts CCG, Calderdale CCG, Greater Huddersfield CCG, Leeds North CCG, Leeds South and East CCG, Leeds West CCG, North Kirklees CCG, Wakefield CCG) will be eligible to participate in the trial provided they use the IT System, SystmOne clinical software for patient health records.

Exclusion criteria

Exclusion criteria: 1. We will exclude the four general practices which participated in earlier pilot intervention work as they will already have been exposed to active intervention components. We will also exclude general practices where we have already interviewed GPs, nurses and practice managers as part of the intervention development process and which participate in the planned qualitative process evaluation (which will be the subject of a further protocol and ethics application). 2. Any general practices that do not use SystmOne software for patient health records will also be excluded.

Design outcomes

Primary

Measure	Time frame
Adherence; Timepoint(s): Adherence will be measures up to 12 mth post randomisaion	—

Countries

England, United Kingdom

Outcome results

None listed