Ohio State University Comprehensive Cancer Center
Columbus, Ohio, 43210, United States
NCT Number: NCT06630442
This clinical trial evaluates the impact of a food safety educational training program on food safety knowledge and behaviors in cancer patients receiving treatment. Cancer treatments, such as chemotherapy, can put patients at risk for foodborne infections and despite this risk, it has been reported that patients do not receive any food safety counseling until they are already experiencing low white blood cell counts. A food safety educational training program may help cancer patients make better choices of low-risk foods and prepare foods safely.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Columbus, Ohio, 43210, United States
PRIMARY OBJECTIVE:
I. Evaluate the efficacy of a food safety education intervention for cancer patients.
OUTLINE:
Patients attend a food safety educational training program over 50 minutes on study.
After completion of study intervention, patients are followed up at 5 weeks.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Attend a food safety educational training program
Other names: Education for Intervention, Intervention by Education, Intervention through Education, Intervention, Educational
Ancillary studies
Time frame: From baseline up to 5 weeks post intervention
Pre and post responses will be determined using score calculation and compared using analysis of variance (ANOVA).
Time frame: From baseline up to 5 weeks post intervention
Pre and post responses will be determined using score calculation and compared using ANOVA.
Time frame: From baseline up to 5 weeks post intervention
Pre and post responses will be determined using score calculation and compared using ANOVA.
Time frame: From baseline up to 5 weeks post intervention
Pre and post responses will be determined using score calculation and compared using ANOVA.
Time frame: From baseline up to 5 weeks post intervention
Pre and post responses will be determined using score calculation and compared using ANOVA.
Time frame: From baseline up to 5 weeks post intervention
Pre and post responses will be determined using score calculation and compared using ANOVA.
Time frame: From baseline up to 5 weeks post intervention
Pre and post responses will be determined using score calculation and compared using ANOVA.
Ohio State University Comprehensive Cancer Center
Other
Efficacy of an Educational Food Safety Intervention for Cancer Patients Receiving Treatment
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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