Prospective Evaluation of the Relation Between Different Questionnaires Measuring Radiation-induced Side-effect

ConditionRadiation
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorM.D. Anderson Cancer Center

About this trial

To learn more about how you would rate the intensity or severity of your symptoms during or after radiation therapy using questionnaires with different rating scales.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥18 years

English as a primary language

Participants with a diagnosis of HNC undergoing active curative RT or having received curative RT within the past 5 years at MD Anderson

Ability to complete the survey(s) of their own volition

Disqualifiers

Age < 18 years

Non-English speaking participants

Participants who are receiving or have received RT in a non-HN site.

Participants in follow up and over 5 years from post-treatment

Trial population

Head and Neck Cancer (HNC) participants undergoing active radiation therapy.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • MDASI-HN

    Other intervention

    Given by Questionnaire

  • EORTC QLQ-C30

    Other intervention

    Given by Questionnaire

  • EORTC HN35

    Other intervention

    Given by Questionnaire

Treatment groups

300 Participants
are divided into 1 treatment group
Group A: Head and Neck Cancer (HNC) Questionnaire3 interventions

Trial outcomes

Primary outcomes

1

Safety and adverse events (AEs)

Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE)

Time frame
Through study completion; an average of 1 year

Secondary outcomes

Other outcomes

Sponsors and contacts

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