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N/A N=85 Randomized Prevention

Food Pantry Client and Staff Preferences for Nutritious no Prep Ready-to-eat Meals

Diet, Healthy · Food Security

Enrolled (actual)
85
Serious AEs
0.0%
Results posted
Mar 2025
Primary outcome: Primary: Hedonic Liking of Study Foods — 7.2; 7.2 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
No prep ready-to-eat meals (Behavioral); Ingredient bundles (e.g. meal kits) (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Texas Southwestern Medical Center
Primary completion
Apr 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Hedonic Liking of Study Foods
7.2; 7.2
PRIMARY
Satisfaction of Study Foods
15.74; 17.29
SECONDARY
Perceived Diet Quality
3.10; 3.4

Summary

The specific aims of this pilot study are: Aim 1) To identify whether no prep ready to eat meals (intervention) or ingredient bundles (control) have higher client acceptability, liking, satisfaction, and perceived diet quality ratings. Aim 2) To identify whether no prep ready to eat meals (intervention) or ingredient bundles (control) have higher feasibility ratings with food pantry staff. Exploratory Aim) To identify whether no prep ready to meals (intervention) or ingredient bundles (control) lead to greater improvements in food security, perceived diet quality, and fruit and vegetable consumption.

Eligibility Criteria

Inclusion Criteria

  • 18 years of age or older;
  • ability to read, write, and speak English or Spanish;
  • ability to provide informed consent;
  • current or new pantry user at our community partner;
  • willing to participate;
  • no dietary restrictions, allergies, or sensitivities that would put the participant at-risk of harm from consuming study foods.

Exclusion Criteria

  • Under 18 years of age;
  • inability to read, write, and speak English or Spanish;
  • unable to provide informed consent;
  • not a pantry user at our community partner or uninterested in becoming a pantry user;
  • not wanting to participate;
  • dietary restrictions, allergies, or sensitivities that would put the participant at-risk of harm from consuming study foods.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05593510). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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