Ignite Creation Date:
2025-12-24 @ 11:53 PM
Ignite Modification Date:
2025-12-25 @ 9:48 PM
Study NCT ID:
NCT04597151
Status:
COMPLETED
Last Update Posted:
2023-01-09
First Post:
2020-10-14
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Diet Education Program for Stage I-IV Colorectal Cancer Survivors
Sponsor:
University of California, San Francisco
Organization:
Study Overview
Official Title:
Diet Education Among Colorectal Cancer Survivors in the Safety Net Setting: A Pilot Feasibility Study
Status:
COMPLETED
Status Verified Date:
2022-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This pilot trial evaluates the feasibility of a group diet education program for stage I-IV colorectal cancer survivors. Providing a nutrition education program for colon and rectal cancer survivors may help them have better access to the tools necessary to make healthy food decisions that can impact their cancer outcomes.
Detailed Description:
PRIMARY OBJECTIVE:
I. To describe the feasibility and acceptability of a group diet education intervention for colorectal cancer (CRC) survivors at Zuckerberg San Francisco General Hospital (ZSFGH).
SECONDARY OBJECTIVE:
I. To describe perceived barriers to healthy diet among CRC survivors at ZSFGH.
EXPLORATORY OBJECTIVES:
I. To evaluate for differences in feasibility and acceptability of a group diet education program, based on sociodemographic factors such as education, food insecurity, employment, and race.
II. To explore changes in health-related behaviors pre and post intervention using a validated lifestyle score.
OUTLINE:
Patients attend group diet education sessions over 1.5-2 hours every 2 weeks (weeks 1, 3, and 5).
After completion of study, patients are followed up at 12 weeks.
I. To describe the feasibility and acceptability of a group diet education intervention for colorectal cancer (CRC) survivors at Zuckerberg San Francisco General Hospital (ZSFGH).
SECONDARY OBJECTIVE:
I. To describe perceived barriers to healthy diet among CRC survivors at ZSFGH.
EXPLORATORY OBJECTIVES:
I. To evaluate for differences in feasibility and acceptability of a group diet education program, based on sociodemographic factors such as education, food insecurity, employment, and race.
II. To explore changes in health-related behaviors pre and post intervention using a validated lifestyle score.
OUTLINE:
Patients attend group diet education sessions over 1.5-2 hours every 2 weeks (weeks 1, 3, and 5).
After completion of study, patients are followed up at 12 weeks.
Study Oversight
Has Oversight DMC:
False
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
Secondary ID Infos
| Secondary ID | Type | Domain | Link | View |
|---|---|---|---|---|
| NCI-2020-06808 | REGISTRY | CTRP (Clinical Trial Reporting Program) | View |