EVEREST-HN 1: EVolution of a patiEnt-REported Symptom-based Risk Stratification sySTem

NCT ID: NCT05909020

Last Updated: 2023-10-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

165 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-03-17

Study Completion Date

2023-11-30

Brief Summary

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Can a patient-reported symptom-based risk stratification system improve the suspected head and neck cancer (HNC) pathway?

Our methodology includes six interlinked work packages to deliver our aim, with EVEREST-HN 1 encompassing the first of these and seeking to optimise a patient-reported symptom inventory for HNC and outline requirement specification for the SYmptom iNput Clinical (SYNC) system.

Detailed Description

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The EVEREST-HN pathway should be based on a comprehensive understanding of existing HNC diagnostic pathways and what patients and clinicians value in these. The language used within the EVEREST pathway needs to be accessible and optimal to elicit appropriate information.

Conditions

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Head and Neck Cancer

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients

Approximately 150 adults referred for suspected HNC will be recruited.

No intervention.

Intervention Type OTHER

No intervention.

Staff

Approximately 15 ENT and Maxillofacial) clinicians will be recruited.

No intervention.

Intervention Type OTHER

No intervention.

Interventions

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No intervention.

No intervention.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

Patients:

* Adults ≥ 18 years referred via suspected HNC pathway without previous history of HNC
* Participants willing and able to give informed consent for participation in the study.

Clinicians:

* Staff at participating sites involved in the diagnostic pathway for people with suspected HNC.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Leeds

OTHER

Sponsor Role collaborator

Royal Marsden NHS Foundation Trust

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Vinidh Paleri

Role: STUDY_CHAIR

Royal Marsden NHS Foundation Trust

Locations

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Leeds Teaching Hospitals NHS Trust

Leeds, , United Kingdom

Site Status NOT_YET_RECRUITING

Liverpool University Hospitals NHS Foundation Trust

Liverpool, , United Kingdom

Site Status RECRUITING

Luton & Dunstable University Hospital

Luton, , United Kingdom

Site Status RECRUITING

Oxford NHS Foundation Trust

Oxford, , United Kingdom

Site Status RECRUITING

Countries

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United Kingdom

Central Contacts

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Sarah Webb

Role: CONTACT

0208 915 6666

Facility Contacts

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Unknown Unknown

Role: primary

Shirley Pringle

Role: primary

Nithin George

Role: primary

Iqbal Mohammed

Role: primary

Other Identifiers

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CCR5683

Identifier Type: -

Identifier Source: org_study_id

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