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Collection of Head Images During Radiotherapy

Collection of Head Images During Radiotherapy (CHIRP)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05218824
Acronym
CHIRP
Enrollment
32
Registered
2022-02-01
Start date
2022-02-14
Completion date
2024-12-31
Last updated
2026-05-19

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

Conditions

Head and Neck Neoplasms, Radiation Therapy Complication

Brief summary

The primary objective of this observational study is to quantify the translation, rotation, and deformation of patient head positions of head and neck cancer patients over the course of a radiation therapy treatment for head and neck cancer. This objective will be achieved by comparing X-ray images collected during each treatment session with those obtained from the planning CT scan. Secondary objectives include (1) the use of the collected X-ray images to develop realistic artificial X-ray images where patient movement can be simulated and (2) to determine whether motion can be detected from individual X-ray images acquired during radiation therapy treatment.

Detailed description

Participants will undergo their radiation therapy treatment for HNC as planned and per the routine clinical management protocol. As part of this routine treatment, multiple x-ray images will be acquired to assist in accurate positioning of the patient for their planned radiation therapy. Normally these images are stored for a few days and then discarded. This study will be collating, storing and analysing these images. These X-ray images will be paired with the corresponding pre-treatment CT scan that is routinely acquired for each patient, as well as the locations of organs of interest, such as the tumour and surrounding structures. The patient treatment plan will also be collated, as it will allow for analysis of how any motion affects the accuracy of dose delivery. The patient radiation treatment delivery record will be collected to help sort and categorise the acquired images. Information on potential confounding or interacting factors will be collected: demographic information will be collected including sex, age, tumour stage and histology.

Interventions

None listed

Sponsors

University of Sydney
Lead SponsorOTHER
Western Sydney Local Health District
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* A diagnosis of head and neck cancer (any stage) * Age 18 years or greater * Receiving radiation therapy to the head and neck with a thermoplastic immobilisation mask * An ECOG score in the range of 0 to 2 * Any other prior or concurrent therapy allowed

Exclusion criteria

* People with cognitive impairment which would preclude them from providing informed consent * People who are unable to speak and read English and for whom obtaining consent would be difficult.

Design outcomes

Primary

MeasureTime frameDescription
Translational head motion between different radiation therapy treatment sessions8 weeksTranslation error (mm)
Rotational head motion between different radiation therapy treatment sessions8 weeksRotation error (degree)
Head deformation between different radiation therapy treatment sessions8 weeksDeformation error (mm)

Secondary

MeasureTime frameDescription
Difference in structural similarity (SSIM) indexes between artificial and real X-rays8 weeksImage quality metric: Structural Similarity (SSIM) index.
Difference in mean absolute error between artificial and real X-rays8 weeksImage quality metric: Mean Absolute Error.

Countries

Australia

Contacts

STUDY_CHAIRPaul Keall, PhD

University of Sydney

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 20, 2026