- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05880004
Developing a Support Application for Food Pantries (SAFPAS) to Improve Client Access to Healthy Foods & Enhance Emergency Preparedness (SAFPAS)
October 6, 2023 updated by: Johns Hopkins Bloomberg School of Public Health
Food pantries face many challenges, including recruitment and training of staff/volunteers, communications with staff/volunteers and clients, providing client choice, and emergency preparedness.
The investigators will develop, implement, and evaluate the Support Application for Food Pantries (SAFPAS), a mobile application to address these concerns under normal and emergency operations, and assess its impact on 20 Baltimore food pantries, and on the healthiness of foods received by 360 food pantry clients using a randomized controlled trial design.
If successful, the tested and refined app will support local food assistance programs throughout the United States.
Study Overview
Status
Recruiting
Conditions
Study Type
Interventional
Enrollment (Estimated)
537
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Cara Shipley, BS
- Phone Number: (410)502-6961
- Email: cshiple9@jhu.edu
Study Locations
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-
Maryland
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Baltimore, Maryland, United States, 21205
- Recruiting
- Johns Hopkins University
-
Contact:
- Joel Gittelsohn, PhD
- Phone Number: 410-955-3927
- Email: jgittel1@jhu.edu
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Contact:
- Lisa Poirier, MHS
- Phone Number: 4105026971
- Email: lpoirie4@jh.edu
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Regular client of the food pantry (visit food pantry/order from one or more participating food pantries at least 1 time/month), for the past year, identified by food pantry personnel Adult (18 years or older)
- Willing and able to use a mobile app through a smart phone (or other device) for making electronic Choice (echoice) selections and engaging in other communications
Exclusion Criteria:
- Anticipate moving out of Baltimore in the next 12 months (for pilot study)
- Pregnant (due to changes in diet, weight and body composition)
- Medically or behaviorally at risk as indicated by the food pantry
- No access to a smart phone or other web-enabled device and Wi-Fi
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Food Pantries receiving SAFPAS intervention
Food Pantries in this arm will receive access to all functions of the SAFPAS application
|
The primary intervention is a mobile application (app) which supports food pantries to recruit, train and schedule volunteers; provide a safe, remote form of client choice; and provides a means of sharing real-time status information with clients, pantries, food banks, and emergency operation centers.
Following formative work, user centered design, and usability testing, the SAFPAS app will be implemented in three stages, where each stage introduces new features.
Pantry clients will be encouraged to download the app and learn its key features at the end of baseline data collection.
During the first weeks of each stage, training of participating food pantry directors/staff and Maryland Food Bank (MFB) staff will take place - focusing on use of any new features.
Initial training will be follow up by proficiency testing.
|
No Intervention: Food Pantries not receiving SAFPAS intervention
Food Pantries in the arm will not receive access to the SAFPAS application
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Client FAST Scores as assessed by the Food Assessment Scoring Tool (FAST)
Time Frame: 1 hour, 14 months
|
Food Assessment Scoring Tool (FAST)(91) scores of client bags from pantries will be captured by the FAST scoring tool at baseline and post-treatment in a sample of 360 client bags (18 clients customers/pantry in 10 intervention and 10 control pantries, at baseline).
Scores can range from 0-100 and are calculated based on the total weight and healthfulness of foods and beverages from 13 categories.
|
1 hour, 14 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Joel Gittlesohn, PhD, Johns Hopkins Bloomberg School of Public Health
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 14, 2023
Primary Completion (Estimated)
April 30, 2025
Study Completion (Estimated)
July 31, 2025
Study Registration Dates
First Submitted
May 19, 2023
First Submitted That Met QC Criteria
May 19, 2023
First Posted (Actual)
May 30, 2023
Study Record Updates
Last Update Posted (Estimated)
October 9, 2023
Last Update Submitted That Met QC Criteria
October 6, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1R34HL161566-01A1 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
De-identified data will be shared on request after signing a data use agreement.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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