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Sample size in multistakeholder Delphi surveys: at what minimum sample size do replicability of results stabilize?
Manyara, Anthony Muchai; Purvis, Anthony; Ciani, Oriana; Collins, Gary S; Taylor, Rod S.
Afiliação
  • Manyara AM; School of Health and Wellbeing, University of Glasgow, Glasgow, UK; Global Health and Ageing Research Unit, Bristol Medical School, University of Bristol, Bristol, UK. Electronic address: Anthony.Manyara@bristol.ac.uk.
  • Purvis A; School of Health and Wellbeing, University of Glasgow, Glasgow, UK.
  • Ciani O; Centre for Research on Health and Social Care Management, SDA Bocconi School of Management, Milan, Italy.
  • Collins GS; UK EQUATOR Centre, Centre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology & Musculoskeletal Sciences, University of Oxford, Oxford, UK.
  • Taylor RS; MRC/CSO Social and Public Health Sciences Unit & Robertson Centre for Biostatistics, School of Health and Wellbeing, University of Glasgow, Glasgow, UK.
J Clin Epidemiol ; 174: 111485, 2024 Jul 26.
Article em En | MEDLINE | ID: mdl-39069013
ABSTRACT
BACKGROUND AND

OBJECTIVE:

The minimum sample size for multistakeholder Delphi surveys remains understudied. Drawing from three large international multistakeholder Delphi surveys, this study aimed to 1) investigate the effect of increasing sample size on replicability of results; 2) assess whether the level of replicability of results differed with participant characteristics for example, gender, age, and profession.

METHODS:

We used data from Delphi surveys to develop guidance for improved reporting of health-care intervention trials SPIRIT (Standard Protocol Items Recommendations for Interventional Trials) and CONSORT (Consolidated Standards of Reporting Trials) extension for surrogate end points (n = 175, 22 items rated); CONSORT-SPI [CONSORT extension for Social and Psychological Interventions] (n = 333, 77 items rated); and core outcome set for burn care (n = 553, 88 items rated). Resampling with replacement was used to draw random subsamples from the participant data set in each of the three surveys. For each subsample, the median value of all rated survey items was calculated and compared to the medians from the full participant data set. The median number (and interquartile range) of medians replicated was used to calculate the percentage replicability (and variability). High replicability was defined as ≥80% and moderate as 60% and <80%

RESULTS:

The average median replicability (variability) as a percentage of total number of items rated from the three datasets was 81% (10%) at a sample size of 60. In one of the datasets (CONSORT-SPI), a ≥80% replicability was reached at a sample size of 80. On average, increasing the sample size from 80 to 160 increased the replicability of results by a further 3% and reduced variability by 1%. For subgroup analysis based on participant characteristics (eg, gender, age, professional role), using resampled samples of 20 to 100 showed that a sample size of 20 to 30 resulted to moderate replicability levels of 64% to 77%.

CONCLUSION:

We found that a minimum sample size of 60-80 participants in multistakeholder Delphi surveys provides a high level of replicability (≥80%) in the results. For Delphi studies limited to individual stakeholder groups (such as researchers, clinicians, patients), a sample size of 20 to 30 per group may be sufficient.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Clin Epidemiol Assunto da revista: EPIDEMIOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Clin Epidemiol Assunto da revista: EPIDEMIOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos