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Educational Video for Cancer Understanding
N/A
Recruiting
Led By Daniel G Stover, MD
Research Sponsored by Ohio State University Comprehensive Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be >= 18 years of age
Be undergoing clinical tumor or circulating tumor deoxyribonucleic acid (DNA) NGS
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediately before and immediately after video intervention
Awards & highlights
Study Summary
This trial is testing whether a video can help patients understand genomic testing for metastatic cancer. Results may help doctors provide better patient care by communicating the importance of this type of testing.
Who is the study for?
This trial is for adults over 18 with metastatic cancer who are undergoing tumor DNA sequencing. It's designed to see if a video can help them understand their genomic testing better. Participants must speak English or Spanish, and have confirmed biopsy results.Check my eligibility
What is being tested?
The study is evaluating the effectiveness of an educational video intervention on patients' comprehension of tumor genomic testing. The goal is to determine if this approach can enhance patient-centered care by improving communication about genomic tests.See study design
What are the potential side effects?
Since the interventions include health education and questionnaire administration, there are no direct medical side effects associated with typical drugs or treatments; however, participants may experience stress or anxiety related to learning about their condition.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 years old or older.
Select...
I am currently having genetic testing on my cancer.
Select...
My cancer has spread, confirmed by a biopsy.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ immediately before and immediately after video intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~immediately before and immediately after video intervention
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Message-specific knowledge/recall accuracy
Secondary outcome measures
Change in patient genomic knowledge
Change in patient genomic knowledge in metastatic breast cancer (MBC) versus metastatic lung cancer (MLC) patients
Change in patient trust of physician/provider
+1 moreSide effects data
From 2020 Phase 3 trial • 177 Patients • NCT0181707513%
Rash maculo-papular
10%
Skin and subcutaneous tissue disorders - Other, specify
1%
Mucositis oral
1%
Sepsis
1%
Skin ulceration
1%
Urticaria
100%
80%
60%
40%
20%
0%
Study treatment Arm
Arm I (CHG Cleansing Wipe)
Arm II (Control)
Trial Design
1Treatment groups
Experimental Treatment
Group I: Health services research (video)Experimental Treatment2 Interventions
Patients participate in a video intervention session and complete questionnaires at baseline, after participating in the video intervention, and after receiving NGS results.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Health Education
2014
Completed Phase 3
~4010
Find a Location
Who is running the clinical trial?
National Cancer Institute (NCI)NIH
13,663 Previous Clinical Trials
40,925,680 Total Patients Enrolled
Ohio State University Comprehensive Cancer CenterLead Sponsor
320 Previous Clinical Trials
289,942 Total Patients Enrolled
Daniel G Stover, MDPrincipal InvestigatorOhio State University Comprehensive Cancer Center
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My cancer has spread, confirmed by a biopsy.I am 18 years old or older.I am currently having genetic testing on my cancer.I speak English or Spanish.
Research Study Groups:
This trial has the following groups:- Group 1: Health services research (video)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
What is the total cohort size of this clinical trial?
"Affirmative, the information held on clinicaltrials.gov confirms that this trial is still seeking participants as of April 18th 2022. Initially posted on April 6th, it requires 225 individuals to be enrolled from a single site."
Answered by AI
Are there any available appointments for this medical experiment?
"Affirmative. Clinicaltrials.gov indicates that this trial, which was first published on April 6th 2022 and is actively enrolling participants, needs 225 people to join from 1 medical site."
Answered by AI
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