Trial · NCT07901816
Optimal Defaults Grocery Shopping Intervention to Promote Healthy Diets for Pediatric Cancer Survivors and Their Families
NCT07901816, Not applicable, Recruiting, Roswell Park Cancer Institute
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Optimal Defaults Grocery Shopping Intervention to Promote Healthy Diets for Pediatric Cancer Survivors and Their Families. Trials, record NCT07901816. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07901816
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Optimal Defaults Grocery Shopping Intervention to Promote Healthy Diets for Pediatric Cancer Survivors and Their Families
- NCT number
- NCT07901816
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 160 participants, estimated
- Lead sponsor
- Roswell Park Cancer Institute
- Conditions
- Pediatric
- Interventions
- Dietary Intervention - meal recipes, Informational Intervention, Educational Intervention, Dietary Intervention - prefilled grocery cart
- First posted
- 2026-10-28
- Last updated
- 2026-11-10
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Retention Rate | At 4 weeks | Percentage of study cohort who complete the study |
| Primary | Percentage of Interested families Eligible for study | At 4 weeks | Feasibility defined as ≥ 50% of interested families being eligible for the study |
| Primary | Percentage of eligible families enrolling in study | At week 4 | Feasibility defined as ≥ 50% of eligible families enrolling |
| Primary | Percent of enrolled families completing baseline measures and proceeding to randomization | At 4 weeks | Feasibility defined as ≥ 90% of enrolled families successfully completing baseline measures and proceeding to randomization |
| Primary | Percentage of randomized families completing the study | At 4 weeks | Feasibility defined as ≥ 85% of randomized families completing the study. |
| Primary | Participant reported interest in continuing to engage in program over a longer period of time. | At 4 weeks | As reported by participants by Phone call |
| Secondary | Change in household grocery purchases: nutritional quality | From baseline to end of study - up to 4 weeks | Nutritional quality will be calculated based on quintiles for each of 13 indicators that correspond to the Healthy Eating Index: total fruit, whole fruit, total vegetables, dark green and legume vegetables, whole grains, dairy, total protein foods, seafood and plant proteins, the ratio of mono and polyunsaturated fatty acids to saturated fatty acids, refined grains, sodium, added sugars, and saturated fats. Quintile scores will be summed to generate nutritional quality of grocery purchases each week |
| Secondary | Changes in household grocery purchases: energy content | UP to 4 weeks | Total energy content of groceries purchased for the household each week |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07901816
GET https://conductscience.org/api/trials/v1/NCT07901816/registered