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Effects of Population Compared to Purposive Sampling for Consensus in an Online Delphi Study

Effects of Population Compared to Purposive Sampling for Consensus in an Online Delphi Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03505450
Enrollment
385
Registered
2018-04-23
Start date
2018-05-29
Completion date
2018-10-29
Last updated
2021-03-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Behavior, Consumer

Keywords

decision support tools,

Brief summary

This study will be nested as a randomized controlled trial within an online Delphi and will assess the effects of the population sampling compared to purposive sampling for consensus in an online Delphi.

Detailed description

The Delphi method of engaging panels of experts from specific interest areas has been widely utilized in the for the development of research reporting guidelines, core outcome sets, clinical medicine, nursing practice, medical education and healthcare services. An assessment completed by Atkins and colleagues in 2005 report that a small panel of similarly trained experts can develop reliable criteria that inform judgment and support effective decision-making. Despite the wide applicability of the Delphi methodology, it is not known how the number of participants or their similarity as a stakeholder group influences results in an online Delphi.Purposeful sampling will be used with a randomized sample taken from each stakeholder group for analysis and this analysis will be presented alongside the full analysis and the results compared. The Protocol Lab for Online Trials-Delphi (PLOT-D), which will use an online 3-round Delphi combined with participatory action research to inform the development of a multi-use protocol template for writing protocols for self-recruited online trials of interventional self-management. The Protocol lab will use the Delphi findings, along with earlier research to redesign a series of protocols for online randomized trials with the aim of providing support for citizens to work alongside researchers to build participatory health trials online.

Interventions

OTHERPurposive sample

purposive sample of recruited participants

OTHERPopulation Sample

full sample of recruited participants

Sponsors

ThinkWell
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Protocol lab online trials Delphi (PLOT-D) Participant

Exclusion criteria

* None if meets inclusion criteria

Design outcomes

Primary

MeasureTime frameDescription
Delphi response rate differences as measured by % of completed questions between samplesUp to 20 weeks or study completionFull Delphi sample compared to a 10% randomized stratified sample taken from of the 5 stakeholder groups

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026