Protocol of an International Delphi Process

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Basel, Switzerland

About this trial

The aim of this study is to develop a consensus-based protocol for medical screening in patients presenting with acute psychiatric symptoms. Using the Delphi method, the study seeks to identify which medical evaluations should be performed routinely in this patient population and under what circumstances. By engaging a panel of experts, the study aims to reduce variability in current practice and support the development of a standardized, evidence-informed approach.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

proficient in English

possess prior experience with medical screening processes in the Emergency Department

Disqualifiers

None

Trial population

interdisciplinary group from national and international societies in emergency medicine and psychiatry on 5 continents and patient representatives * Patient representatives: at least 6 in total; can include patients, patient relatives, caregivers, organizations, experts, or advocates * society representatives: national and international societies for emergency medicine and psychiatry from North America, South America, Europe, and Australasia, 3 representatives per region, at least 12 in total; strong interest in medical screening with a proven track record in emergency psychiatry and/or current employment in an emergency psychiatry setting

Trial design

Design model

Ecologic or community

Time perspective

Prospective

Treatments tested in this trial

  • Delphi Consensus Process

    Other intervention

    Round 1: Evaluation of current Medical Screening Tools and Scoping Review Results Round 2: Rating previous Statements from Round 1 Round 3: Consensus Round 4: Testing Content and Construct Validity of the new Medical Screening Tool with Clinical Vignettes

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Consensus regarding items for the new medical screening tool

Consensus is define as agreement over a pre-set benchmark of ≥80% agreement. If ≥80% of the responses of all participants to a variable indicate "agree", "strongly agree" or "very strongly agree" in the final round of this Delphi study, it is considered consensus that the variable will be kept.

Time frame
through study completion, an average of 7 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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