Developing and agreeing the Life After Stroke Set of Outcomes (LASSO): A core outcome set

There is an urgent need to improve life after stroke. However, the evidence base is undermined by poor and uncoordinated outcome measurement. An agreed and standardised set of essential outcomes (Core Outcome Set (COS)) for use in effectiveness trials is required, informed by knowledge of the outcomes that matter most to stroke survivors, families and other clinical decision makers.

Methods:
Stage I: Identification of outcomes that may be relevant for life after stroke encompassing those used in stroke trials via a systematic review and those discussed by stroke survivors and carers via an overview of qualitative systematic reviews.
Stage II: Agreement of COS via (1) A Q methodology study with stroke survivors and carers to identify their perspectives on priority outcomes (2) A Delphi study with professionals and (3) Final agreement at a consensus conference.
Stage III: Identification of candidate measures for each of the core outcomes via systematic review.

Expected outcomes:
An agreed COS, reflecting the outcomes that matter most to stakeholders, candidate measures for these outcomes and an agenda for further research. The COS should be measured and reported in all relevant effectiveness trials enabling future meta-analysis, an enhanced evidence base and improvement in life after stroke.

Contributors

Tom Crocker [1]: Chief investigator
Anne Forster [1,2]: Supervisor
David Clarke [1,2]: Supervisor
Janet Holt [3]
Barbara Brown: Consumer expert

1: Academic Unit of Elderly Care & Rehabilitation, Bradford Institute for Health Research, Bradford Teaching Hospitals NHS Foundation Trust
2: Academic Unit of Elderly Care & Rehabilitation, Leeds Institute of Health Sciences, University of Leeds
3: School of Healthcare, University of Leeds

Further Study Information

Current Stage: Ongoing
Date: July 2018 - November 2021
Funding source(s): TBC


Health Area

Disease Category: Neurology

Disease Name: Stroke

Target Population

Age Range: 16 - 100

Sex: Either

Nature of Intervention: Any

Stakeholders Involved

- Charities
- Clinical experts
- Consumers (caregivers)
- Consumers (patients)
- Researchers
- Service commissioners

Study Type

- COS for clinical trials or clinical research

Method(s)

- Consensus conference
- Delphi process
- Literature review
- Nominal group technique (NGT)
- Other
- Systematic review

Other: Q methodology

Stage I: Identification of outcomes that may be relevant for life after stroke encompassing those used in stroke trials via a systematic review and those discussed by stroke survivors and carers via an overview of qualitative systematic reviews.
Stage II: Agreement of COS via (1) A Q methodology study with stroke survivors and carers to identify their perspectives on priority outcomes (2) A Delphi study with professionals and (3) Final agreement at a consensus conference.
Stage III: Identification of candidate measures for each of the core outcomes via systematic review.

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