Can a smartphone app ease the stress of food insecurity for mothers?
NCT ID NCT07718646
First seen Jul 22, 2026 · Last updated Jul 23, 2026 · Updated 1 time
Summary
This pilot study tests whether an 8-week mobile app called MOMent can help mothers who are experiencing food insecurity build coping skills and reduce stress. The app uses techniques from cognitive behavioral therapy (CBT), including goal-setting, self-monitoring, and skill-building reflections. Participants will use the app and complete surveys about their mental health and coping. The study aims to see if the app is practical and acceptable for future, larger research.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- an 8-week mobile app behavioral intervention called MOMent that teaches coping strategies, goal-setting, and self-monitoring
- What this could lead to
- If the app proves helpful and easy to use, it could offer a low-cost way to support mental well-being for mothers facing food insecurity.
- What could go wrong
- This is a very small pilot study with only 30 participants, so results may not apply broadly. The app requires a smartphone, which could limit access.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Reside in Oklahoma * Identify as a woman or non-binary * At least 18 years old * Have a child under 18 years old living in your household * Experienced food insecurity in the past 30 days Exclusion Criteria: * Currently undergoing mental health counseling * No access to a smartphone (Apple or Android)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Oklahoma State University
RECRUITINGStillwater, Oklahoma, 74078, United States
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