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A Video Intervention to Improve Patient Understanding of Tumor Genomic Testing in Patients With Metastatic Cancer

The Ohio State University logo

The Ohio State University

Status

Active, not recruiting

Conditions

Anatomic Stage IV Breast Cancer AJCC v8
Prognostic Stage IV Breast Cancer AJCC v8
Stage IVA Lung Cancer AJCC v8
Metastatic Malignant Solid Neoplasm
Metastatic Breast Carcinoma
Metastatic Lung Carcinoma
Stage IVB Lung Cancer AJCC v8
Stage IV Lung Cancer AJCC v8

Treatments

Other: Questionnaire Administration
Behavioral: Health Education

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05215769
NCI-2021-13900 (Registry Identifier)
OSU-21313
R21CA259985 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This clinical trial tests whether a video intervention improves patient understanding of tumor genomic testing in patients with cancer that has spread to other parts of the body (metastatic). Measuring how the video intervention affects patient understanding of tumor genomic testing in patients with metastatic cancer may help doctors provide patient-centered care by effectively communicating the importance of tumor genomic testing.

Full description

PRIMARY OBJECTIVE:

I. To assess change in patient knowledge about tumor next generation sequencing (NGS) following exposure to the video.

SECONDARY OBJECTIVES:

I.To assess changes following exposure to the video, including; Ia. Genomic knowledge via the validated 10 true/false question survey (% correct out of 10).

Ib. 11-item Trust in Physician Survey (TPS) as a single TPS score. Ic. Comparison of results in three patient cohorts: 1) Metastatic breast cancer; 2) lung cancer; 3) metastatic cancer of unspecified type.

EXPLORATORY OBJECTIVE:

I. Assess whether therapies prescribed as a result of tumor NGS achieved clinically favorable result through chart review.

OUTLINE:

Patients participate in a video intervention session and complete questionnaires at baseline, after participating in the video intervention, and after receiving NGS results.

Enrollment

243 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients must have biopsy-confirmed metastatic cancer
  • Be >= 18 years of age
  • Be undergoing clinical tumor or circulating tumor deoxyribonucleic acid (DNA) NGS

Exclusion criteria

  • Exclude patients who are not English- or Spanish-speaking

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

243 participants in 1 patient group

Health services research (video)
Experimental group
Description:
Patients participate in a video intervention session and complete questionnaires at baseline, after participating in the video intervention, and after receiving NGS results.
Treatment:
Behavioral: Health Education
Other: Questionnaire Administration

Trial contacts and locations

4

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Central trial contact

The Ohio State University Comprehensive Cancer Center

Data sourced from clinicaltrials.gov

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