Patient-Reported Outcomes in Head and Neck Cancer

NCT03918382 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 291

Last updated 2023-10-27

No results posted yet for this study

Summary

Weekly electronic reporting of patient-reported outcomes will be tested in a national trial in participants undergoing radiotherapy for head and neck cancer.

The study is a national study under the Danish Head and Neck Cancer Group (DAHANCA) and all 6 centers in Denmark will participate.

The clinical endpoints will be:

* Quality of life
* Objective toxicity score (DAHANCA)
* Opioid treatment
* Tube feeding
* Weight loss
* Hospitalization
* Compliance to treatment

Conditions

Interventions

OTHER

Electronic Patient-Reported Outcome

Weekly reporting of patient-reported outcomes on a tablet for closer contact between patient and clinic during radiotherapy.

Sponsors & Collaborators

  • Danish Comprehensive Cancer Center

    collaborator OTHER
  • Danish Cancer Society

    collaborator OTHER
  • University of Copenhagen

    collaborator OTHER
  • Danish Head and Neck Cancer Group

    collaborator NETWORK
  • Herlev Hospital

    collaborator OTHER
  • Zealand University Hospital

    collaborator OTHER
  • Odense University Hospital

    collaborator OTHER
  • Aalborg University Hospital

    collaborator OTHER
  • Aarhus University Hospital

    collaborator OTHER
  • Rigshospitalet, Denmark

    lead OTHER

Principal Investigators

  • Cecilie Holländer-Mieirtz, MD · Rigshospitalet, Denmark

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-06-13
Primary Completion
2024-03-01
Completion
2024-08-01

Countries

  • Denmark

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03918382 on ClinicalTrials.gov