A Multilevel Intervention in the Hunger Relief Network to Improve Diet Among Adults Experiencing Food Insecurity (SuperShelf)
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|ClinicalTrials.gov Identifier: NCT03421106|
Recruitment Status : Terminated (Data collection was halted prematurely due to COVID-19.)
First Posted : February 5, 2018
Last Update Posted : October 8, 2021
|Condition or disease||Intervention/treatment||Phase|
|Food Selection||Behavioral: Intervention Food Pantries Other: Control Food Pantries||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||504 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Multilevel Intervention in the Hunger Relief Network to Improve Diet Among Adults Experiencing Food Insecurity|
|Actual Study Start Date :||February 5, 2018|
|Actual Primary Completion Date :||September 1, 2019|
|Actual Study Completion Date :||November 16, 2020|
Experimental: Intervention Food Pantries
Food pantries will transform to offer healthier and more appealing food ; the effect on clients will be measured.
Behavioral: Intervention Food Pantries
Food pantries will receive consulting services to transform their food offerings and environment in order to influence client health behaviors.
Active Comparator: Control Food Pantries
Food pantries will make no changes during the evaluation period; the effect on clients will be measured.
Other: Control Food Pantries
Normal food pantry use
- Overall diet quality of clients [ Time Frame: Baseline, 1 year ]Assessed by Healthy Eating Index-2015 scores (scale 0-100), with 100 representing the highest possible score.
- Nutritional quality of food selected by clients at the food pantry [ Time Frame: Baseline, 1 year ]Assessed by Healthy Eating Index-2015 scores (scale 0-100), with 100 representing the highest possible score.
- Cardiovascular health [ Time Frame: Baseline, 1 year ]American Heart Association's Life's Simple 7 (LS7) scores (scale 0 -7), with 7 representing the highest possible score
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03421106
|United States, Minnesota|
|University of Minnesota|
|Minneapolis, Minnesota, United States, 55414|
|Principal Investigator:||Caitlin E Caspi, ScD||University of Connecticut|