The Role of Audiovisual Biofeedback on Image Quality During 4D Anatomic and Functional Imaging

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

10 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-07-31

Study Completion Date

2013-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study will investigate whether audiovisual biofeedback, in which visual and audio cues are used to regulate the patient's breathing, can increase the image quality of 4D CT and 4D PET scans.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Radiolabelled Nectin-4 Targeted LMW Probe PET/CT in Patients With Lung Lesions

NCT06648317

Lung Cancer, Non-Small Cell Lung Infection

RECRUITING

Assessment of 4D 18F-FDG PET-CT in Radiotherapy for Non Small Cell Lung Cancers

NCT01421953

Lung Cancer Non-small-cell Lung Carcinoma

COMPLETED NA

Influence of PET/CT Radiomic Features on the Outcome of Lung Cancer Patients

NCT03648151

Lung Cancer Image, Body

COMPLETED

Utility of Anatometabolic Imaging for Radiation Treatment Planning for Lung Cancer

NCT00005666

Carcinoma, Non-Small-Cell Lung

COMPLETED NA

Improving Clinical PET/CT Image Quality in Retrospectively Reconstructed Breath-Hold Images

NCT01109953

Lung Cancer

TERMINATED

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Lung Cancer

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Real time position management system

Device to monitor respiration by using optical monitoring of a marker block placed on the abdomen of the patient.

Intervention Type DEVICE

LS PET/CT

PET/CT scanner for acquiring CT and PET images (3D and 4D)

Intervention Type DEVICE

18-FDG

15mCi

Intervention Type DRUG

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Varian GE Fludeoxyglucose (18F) fluorodeoxyglucose (18F)

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

Required for inclusion in this study are:

* Informed consent
* Diagnosis of AJCC Stage I-III lung cancer of any histology to be treated using radiotherapy at Stanford Cancer Center
* Age 18 or greater
* Painfree in supine position
* Karnofsky performance status 50 or greater

The inclusion of educationally disadvantaged, decisionally impaired or homeless people are allowed if informed consent, in the opinion of the consenting investigator (study PI, co-PI or research nurse), is obtained.