- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06602999
Addressing the Nutritional Needs of Cancer Survivors With Nutrition Insecurity
Study Overview
Status
Intervention / Treatment
Detailed Description
PRIMARY OBJECTIVE:
I. To determine the intervention's feasibility and acceptability.
SECONDARY OBJECTIVES:
I. To estimate the effect of the intervention on adherence to American Cancer society nutrition guidelines.
II. To estimate the effect of the intervention on self-reported food insecurity.
III. To evaluate the feasibility of patient navigation calls. IV. To evaluate the feasibility of Instacart vouchers.
EXPLORATORY OBJECTIVE:
I. To evaluate the feasibility of the intervention through an end-of-study semi-structured interview.
OUTLINE:
Patients receive a booklet on nutrition and physical activity for cancer survivors and 1 Instacart grocery delivery voucher to use over 4 weeks on study. Patients also receive nutrition navigation phone calls for assistance with following nutrition guidelines and ordering groceries on Instacart once a week (QW) for 4 weeks.
After completion of study intervention, patients are followed up at 28 days.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
-
San Francisco, California, United States, 94143
- University of California, San Francisco
-
San Francisco, California, United States, 94110
- Zuckerberg San Francisco General
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age > 18 years
- Diagnosis of a malignant cancer (except non-melanoma skin cancer).
- Not on active treatment at the time of screening and not expected to receive active anticancer therapy (e.g., surgery, radiation, chemotherapy, immunotherapy, targeted therapies) during the study period. Hormonal therapies are allowed for patients with breast or prostate cancer
- At least 6 weeks since a major surgery and fully recovered.
- Have access to the internet and able to send and receive text messages.
- Able to speak/read English.
Based on the United States Department of Agriculture (USDA) United States (U.S.) Household Food Security Survey, identify as experiencing food insecurity and/or belong to a population that the National Institutes of Health (NIH) has identified as being at risk for health disparities:
- Identify as a racial or ethnic minoritized group, as defined by the NIH (American Indian or Alaska Native, Asian, Black or African American, Native Hawaiian or Pacific Islander, Latino or Hispanic)
- Identify with a sexual or gender minoritized group.
- Annual household income < 200% of the federal poverty definition and/or education < bachelor's degree.
- Live in a rural and/or a persistent poverty area (based on zip code).
Exclusion Criteria:
- Contraindication to any study-related procedure or assessment.
- Planned major surgery or cancer-directed therapy during the study period.
- Living outside of the US or Canada during screening and/or the study period (outside the geographic areas that Instacart covers).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Supportive Care (Instacart voucher, nutrition navigation)
Participants receive a booklet on nutrition and physical activity for cancer survivors and 1 Instacart grocery delivery voucher to use over 4 weeks on study.
Participants also receive nutrition navigation phone calls for assistance with following nutrition guidelines and ordering groceries on Instacart every week for 4 weeks.
|
Receive a booklet on nutrition and physical activity for cancer survivors
Receive Instacart grocery delivery voucher
Other Names:
Receive nutrition navigation phone calls
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Median Score on the Feasibility of Intervention Measure (FIM) Survey
Time Frame: At 4 week assessment, 1 day
|
The FIM is a four-item measure of implementation that assesses participants perceived feasibility of the intervention.
Each item response falls on a scale of 1 (Completely disagree) to 5 (Completely agree).
A total score is calculated by averaging responses.
Total score values range from 1 to 5 with higher values representing a greater feasibility.
The intervention will be determined feasible if the overall median score is >= 4. The median and full range of the FIM scores will be reported.
|
At 4 week assessment, 1 day
|
|
Median Score on the Acceptability of Intervention Measure (AIM) Survey
Time Frame: At 4 week assessment, 1 day
|
The AIM is a four-item measure of implementation that assesses participants perceived acceptability of the intervention.
Each item response falls on a scale of 1 (Completely disagree) to 5 (Completely agree).
A total score is calculated by averaging responses.
Total score values range from 1 to 5 with higher scores indicating a greater acceptability of the intervention.
The intervention will be determined acceptable if the overall median score is >= 4. The median and full range of the AIM scores will be reported.
|
At 4 week assessment, 1 day
|
|
Median Score on the Appropriateness of Intervention Measure (IAM) Survey
Time Frame: At 4 week assessment, 1 day
|
The IAM is a four-item measure of implementation that assesses participants perceived appropriateness of the intervention.
Each item response falls on a scale of 1 (Completely disagree) to 5 (Completely agree).
A total score is calculated by averaging responses.
Total score values range from 1 to 5 with higher scores indicating a higher agreement with the appropriateness of the intervention.
The intervention will be determined appropriate if the overall median score is >= 4. The median and full range of the AIM scores will be reported.
|
At 4 week assessment, 1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Median Score on the Red Meat Category of the Dietary Screener Questionnaire (DSQ) Over Time
Time Frame: Up to 4 weeks
|
The DSQ is a 19-item questionnaire which assesses intakes of fruits and vegetables, whole grains, added sugars, dairy, fiber, and calcium assessment of nutritional intake from the National Health and Nutrition Examination Survey (NHANES) to assess dietary habits.
This brief screener asks participants to report on dietary intake in the past month.
Dietary factors assessed include fruit and vegetables, fiber, whole grains, added sugars, red meat, and processed meat.
The scoring algorithms that convert DSQ data to nutrient and food-group estimates and appropriate analysis programs are available from the NCI (https://epi.grants.cancer.gov/nhanes/dietscreen/scoring/).
A theoretical maximum and/or minimum value for the overall intake scores on the DSQ does not exist.
Change in median overall intake values on the DSQ to assess adherence to the American Cancer Society nutrition guidelines and full range of scores will be used to describe the change of overall adherence over time.
|
Up to 4 weeks
|
|
Change in Median Score on the Processed Meat Category of the Dietary Screener Questionnaire (DSQ) Over Time
Time Frame: Up to 4 weeks
|
The DSQ is a 19-item questionnaire which assesses intakes of fruits and vegetables, whole grains, added sugars, dairy, fiber, and calcium assessment of nutritional intake from the National Health and Nutrition Examination Survey (NHANES) to assess dietary habits.
This brief screener asks participants to report on dietary intake in the past month.
Dietary factors assessed include fruit and vegetables, fiber, whole grains, added sugars, red meat, and processed meat.
The scoring algorithms that convert DSQ data to nutrient and food-group estimates and appropriate analysis programs are available from the NCI (https://epi.grants.cancer.gov/nhanes/dietscreen/scoring/).
A theoretical maximum and/or minimum value for the overall intake scores on the DSQ does not exist.
Change in median overall intake values on the DSQ to assess adherence to the American Cancer Society nutrition guidelines and full range of scores will be used to describe the change of overall adherence over time.
|
Up to 4 weeks
|
|
Change in Median Score on the Whole Grains Category of the Dietary Screener Questionnaire (DSQ) Over Time
Time Frame: Up to 4 weeks
|
The DSQ is a 19-item questionnaire which assesses intakes of fruits and vegetables, whole grains, added sugars, dairy, fiber, and calcium assessment of nutritional intake from the National Health and Nutrition Examination Survey (NHANES) to assess dietary habits.
This brief screener asks participants to report on dietary intake in the past month.
Dietary factors assessed include fruit and vegetables, fiber, whole grains, added sugars, red meat, and processed meat.
The scoring algorithms that convert DSQ data to nutrient and food-group estimates and appropriate analysis programs are available from the NCI (https://epi.grants.cancer.gov/nhanes/dietscreen/scoring/).
A theoretical maximum and/or minimum value for the overall intake scores on the DSQ does not exist.
Change in median overall intake values on the DSQ to assess adherence to the American Cancer Society nutrition guidelines and full range of scores will be used to describe the change of overall adherence over time.
|
Up to 4 weeks
|
|
Change in Median Score on the Sugar-Sweetened Beverages Category of the Dietary Screener Questionnaire (DSQ) Over Time
Time Frame: Up to 4 weeks
|
The DSQ is a 19-item questionnaire which assesses intakes of fruits and vegetables, whole grains, added sugars, dairy, fiber, and calcium assessment of nutritional intake from the National Health and Nutrition Examination Survey (NHANES) to assess dietary habits.
This brief screener asks participants to report on dietary intake in the past month.
Dietary factors assessed include fruit and vegetables, fiber, whole grains, added sugars, red meat, and processed meat.
The scoring algorithms that convert DSQ data to nutrient and food-group estimates and appropriate analysis programs are available from the NCI (https://epi.grants.cancer.gov/nhanes/dietscreen/scoring/).
A theoretical maximum and/or minimum value for the overall intake scores on the DSQ does not exist.
Change in median overall intake values on the DSQ to assess adherence to the American Cancer Society nutrition guidelines and full range of scores will be used to describe the change of overall adherence over time.
|
Up to 4 weeks
|
|
Change in Median Score on the Frut and Vegetable Category of the Dietary Screener Questionnaire (DSQ) Over Time
Time Frame: Up to 4 weeks
|
The DSQ is a 19-item questionnaire which assesses intakes of fruits and vegetables, whole grains, added sugars, dairy, fiber, and calcium assessment of nutritional intake from the National Health and Nutrition Examination Survey (NHANES) to assess dietary habits.
This brief screener asks participants to report on dietary intake in the past month.
Dietary factors assessed include fruit and vegetables, fiber, whole grains, added sugars, red meat, and processed meat.
The scoring algorithms that convert DSQ data to nutrient and food-group estimates and appropriate analysis programs are available from the NCI (https://epi.grants.cancer.gov/nhanes/dietscreen/scoring/).
A theoretical maximum and/or minimum value for the overall intake scores on the DSQ does not exist.
Change in median overall intake values on the DSQ to assess adherence to the American Cancer Society nutrition guidelines and full range will be used to describe the change of overall adherence over time.
|
Up to 4 weeks
|
|
Change in Mean Score on Participant Reported United States Department of Agriculture Food Insecurity Questionnaire
Time Frame: Up to 4 weeks
|
The United States Department of Agriculture Food Insecurity Questionnaire consists of 6 items that address various aspect of food security.
Responses of "often" or "sometimes" and "yes" are coded as affirmative.
Responses of "almost every month" and "some months but not every month" are coded as affirmative.
The sum of affirmative responses to the six questions in the module is the household's raw score on the scale.
Food security status is assigned as follows: Raw score 0-1 = High or marginal food security (raw score=1 may be considered marginal food security, but a large proportion of households that would be measured as having marginal food security using the household or adult scale will have raw score of 0 on the six-item scale), Raw scores of 2-4=Low food security, Raw scores 5-6=Very low food security.
The mean change in raw score over time will be reported along with the standard deviation.
|
Up to 4 weeks
|
|
Proportion of Participants Who Participated in Navigation Calls
Time Frame: Up to 4 weeks
|
The proportion of participants who participated in the weekly navigation calls by total number of calls completed will be reported.
|
Up to 4 weeks
|
|
Proportion of Participants Using Instacart Vouchers
Time Frame: Up to 4 weeks
|
The proportion of participants who utilized the Instacart vouchers during the course of the study will be reported.
|
Up to 4 weeks
|
Collaborators and Investigators
Investigators
- Principal Investigator: Erin Van Blarigan, ScD, University of California, San Francisco
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 24806
- NCI-2024-07163 (Registry Identifier: NCI Clinical Trials Reporting Program (CTRP))
- U54CA280811 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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