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TRacheostomy in DElphi for iNTensive Care' (TRiDENT)

TRacheostomy in DElphi for iNTensive Care' (TRiDENT)

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07481435
Acronym
TRiDENT
Enrollment
40
Registered
2026-03-18
Start date
2026-05-01
Completion date
2026-12-01
Last updated
2026-05-04

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

Conditions

Delphi Process, Delphi Study

Keywords

Intensive Care Medicine, Post Intensive Care

Brief summary

The aim of this study is to develop international consensus-based recommendations for tracheostomy care in critically ill patients. Using the Delphi method, the study seeks to identify key practices in post-tracheostomy management, including tube downsizing and decannulation strategies, infection prevention and site care, restoration of communication and swallowing, and the recognition and management of tracheostomy-related complications. By engaging a multidisciplinary panel of international experts involved in tracheostomy care, the study aims to reduce variability in current practice and support the development of standardized, evidence-informed approaches across different clinical settings.

Detailed description

Background\<br\>\<br\> Tracheotomy is a common intervention in intensive care unit patients, with up to one in every six patients receiving a tracheostomy for weaning from invasive ventilation. Indications for tracheostomy include facilitating liberation from prolonged ventilation, protecting the airway, aiding secretion clearance, and enhancing patient comfort by supporting communication and swallowing. \<br\> Variation in post-tracheotomy care often arises from the different clinical teams involved in tracheostomy care. Depending on local expertise and institutional organization, tracheostomies may be managed by otolaryngologists, intensivists, anesthesiologists, or general surgeons. Tracheostomy management encompasses an entire continuum of care, including decannulation strategies and infection prevention practices, as well as post-ICU follow-up and rehabilitation pathways. \<br\>\<br\> Tracheostomy care lacks standardization, particularly regarding tube downsizing and safe decannulation, infection prevention and tracheostomy site care, and strategies to restore communication, swallowing, and feeding. In addition, timely recognition and management of complications beyond the peri-tracheotomy phase (e.g., posterior glottic stenosis, tracheal stenosis, granuloma formation, airway patency issues), as well as minimum requirements for post-ICU tracheostomy care, are often poorly defined. \<br\>\<br\> These gaps may lead to clinically relevant consequences, including cannula obstruction or dislodgement, delayed decannulation, airway complications, impaired communication, swallowing dysfunction, psychological distress, and increased caregiver burden. \<br\>\<br\> Addressing these domains through expert consensus is crucial to improving patient recovery and quality of life, reducing complications, and ensuring equitable standards of tracheostomy care across different settings. We therefore designed a Delphi study named "TRacheostomy in DEiphi for iNTensive care' (TRiDENT)" to gather and synthesize international multidisciplinary expertise to establish consensus and identify research priorities in tracheostomy care. \<br\>\<br\> Study Design\<br\>\<br\> The TRiDEnt study will utilize a Delphi methodology to achieve consensus or identify areas of disagreement regarding tracheostomy management in intensive care. Reporting of the Delphi process will adhere to the ACcurate COnsensus Reporting Document (ACCORD) guidelines. \<br\>\<br\> A Steering Committee composed of experienced physicians and researchers in tracheostomy and critical care will lead the study. Two members of the Steering Committee will serve as Delphi methodologists. The Steering Committee will perform a focused literature review on post-tracheostomy care in the critical care setting to inform the questions of the initial Delphi round. \<br\>\<br\> The committee will identify and select panelists from global institutions based on predefined eligibility criteria. To facilitate consensus among panelists, the Steering Committee will conduct iterative Delphi rounds, prepare round reports, and modify or add statements based on panelist feedback. Statements reaching consensus and stability will be used to develop clinical practice statements. Steering Committee members will not participate as respondents in the Delphi surveys. \<br\>\<br\> A diverse panel of approximately 35-40 experts will be recruited from multiple disciplines involved in tracheostomy care, including otolaryngology and maxillofacial surgery, intensive care medicine, respiratory medicine, anesthesiology, nursing, respiratory therapy, speech and language therapy, physiotherapy, and physiatry. Panelists will be selected using purposive sampling based on expertise and recent publications in the field. \<br\>\<br\> Potential participants will be invited via email and informed about the study objectives and the Delphi process. Communication will be maintained throughout the study to encourage retention, with reminders sent during each round. Each Delphi round will last approximately two weeks. \<br\>\<br\> Step 1: Establishing Preliminary Domains\<br\>\<br\> Domain 1: Cannula care\<br\> Domain 2: Complication management\<br\> Domain 3: Care trajectories\<br\>\<br\>\<br\> Step 2: Preparation of the Delphi Round 1 Survey\<br\>\<br\> Panelists will receive an online survey containing questions related to the identified domains. Responses will be anonymized to ensure confidentiality and minimize peer pressure and conformity bias. Participants will answer based on their expertise using multiple-choice questions and a 7-point Likert scale. \<br\> Responses and comments will be compiled into a report providing controlled feedback for subsequent rounds.\<br\>\<br\> Step 3: Subsequent Delphi Rounds\<br\>\<br\> The Steering Committee will review the results from each round and modify, remove, or add statements based on feedback. Updated statements will be presented in subsequent rounds until stable consensus or dissensus is achieved. \<br\> Consensus will be defined as ≥75% agreement or disagreement on Likert scale responses and multiple-choice questions.\<br\>\<br\> Step 4: Final Consensus\<br\>\<br\> Results from the final stable round will be used to draft consensus-based statements regarding tracheostomy management.\<br\>\<br\> Patient and Public Involvement\<br\>\<br\> Patient and public involvement is planned to ensure that consensus outcomes reflect not only clinical priorities but also the experiences of individuals living with a tracheostomy and their families.\<br\>\<br\> Economic Considerations\<br\>\<br\> Healthcare economists will contribute to the evaluation of the cost-effectiveness and resource implications of proposed practices, given the substantial economic burden associated with tracheostomy care.

Interventions

Round 1: Evaluation and rating of preliminary statements on tracheostomy care derived from literature review and expert input. Round 2: Re-rating of statements from Round 1 with controlled feedback and modification based on panelist comments. Round 3: Final consensus assessment on remaining statements that did not reach agreement in previous rounds. Round 4: Prioritization and refinement of the final consensus statements to define key recommendations and research priorities in tracheostomy care.

Sponsors

Universita degli Studi di Genova
Lead SponsorOTHER
University of Michigan
CollaboratorOTHER
The Royal Wolverhampton Hospitals NHS Trust
CollaboratorOTHER_GOV
Hospital Israelita Albert Einstein
CollaboratorOTHER
Amsterdam University of Applied Sciences
CollaboratorOTHER
Tribhuvan University Teaching Hospital, Institute Of Medicine.
CollaboratorOTHER
The University of Queensland
CollaboratorOTHER
Federico II University
CollaboratorOTHER
University of Birmingham
CollaboratorOTHER
University of Oxford
CollaboratorOTHER
University Wien
CollaboratorOTHER
Monash University
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* A minimum of 5 years of clinical experience treating patients requiring tracheostomy and leadership in the subject area. * At least 5 publications in the area.

Exclusion criteria

* Not more than 70% of the panellists are of the same gender and from each of high and low-middle-income countries

Design outcomes

Primary

MeasureTime frameDescription
Consensus on statements regarding tracheostomy care in critically ill patientsthrough study completion, an average of 6-8 monthsConsensus is defined as agreement over a pre-set benchmark of ≥75% agreement. If ≥75% of responses from all participants to a given statement indicate agreement (e.g., ratings in the upper categories of the 7-point Likert scale) in the final round of this Delphi study, consensus will be considered achieved and the statement will be retained as part of the final consensus recommendations on tracheostomy care.

Contacts

CONTACTDenise Battaglini, MD
battaglini.denise@gmail.com+390105551
CONTACTMarcus J Schultz, MD, PhD
marcus.j.schultz@gmail.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 5, 2026