Could a 12-Day cooking class beat malnutrition? bangladesh trial aims to find out
NCT ID NCT07591064
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a 12-day nutrition education program, called Positive Deviance/Hearth (PDH), can help children aged 6-59 months recover from moderate acute malnutrition. Caregivers learn to prepare nutrient-dense meals using local ingredients, with follow-up support. The trial will compare recovery rates and relapse in 400 children receiving PDH versus standard care in Bangladesh.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Positive Deviance/Hearth (PDH) behavioral nutrition program
- What this could lead to
- If successful, this could provide a low-cost, sustainable way to treat malnutrition in children using local foods, reducing reliance on specialized supplements.
- What could go wrong
- This is a relatively small trial (400 children) in one region of Bangladesh, so results may not apply elsewhere. The program depends on caregiver participation and local food availability, which could limit effectiveness.
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
-
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
-
About 400 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
May 2026
An estimate. Start dates often move.
- Expected to finish
-
Dec 2026
An estimate. End dates often move.
- Lead sponsor
-
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
-
6 to 59 months
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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: * Children 6-52.9 months at Baseline. This is so that children are 6-59 months by end of study (6-7 months from baseline) * Children with MAM (WHZ/WLZ \<-2 and ≥-3 and/or MUAC \<125mm and ≥115mm) * No Medical Complications (passes IMCI screening questions) * No oedema * Child does not deteriorate to SAM (WHZ/WLZ\<-3 and/or MUAC\<115mm) because child should be referred to health centre * Caregiver refuses to receive age-appropriate immunization, Vitamin A and deworming minimum 2 weeks before PDH begins * Child is not planning to live outside the study area routinely for more than 2 weeks during the 3 months of the study * Written/Oral consent is given by Parent/Caregiver to participate in the study Exclusion Criteria: * Child is not between 6-52 months of age at Baseline * Child does not meet the inclusion criteria for WHZ/WLZ and/or MUAC; (WHZ/WLZ \<-2SD and ≥-3SD and/or MUAC \<125mm and ≥115mm); * Child has oedema; * Child has medical complications and/or does not pass the IMCI screening including fever, nausea/vomiting, acute respiratory illness (refer to Study Protocol V2.0, 19 Feb 2026); * Deteriorates to SAM and must be removed from the study and referred to the health centre for specially formulated food (SFF) treatment; * Refuses to receive minimum 2 weeks before the intervention begins, age-appropriate immunization and Vitamin A and deworming in the past 6 months; * Child lives outside the study area routinely or will be outside of the study area for more than 2 weeks in the upcoming 3 months * Parent/Caregiver unable or unwilling to attend PDH from start; * Parent/Caregiver does not provide written or oral consent to screen for the trial; * Parent/Caregiver does not provide informed consent for the study; and * any other reason.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Moderate acute malnutrition (MAM) are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
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
-
World Vision Bangladesh
Purbadhala, Mymensingh, Bangladesh
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- One diet plan to fight two forms of malnutrition in kids?
- Soothing sounds: a simple audio may help Low-Birth-Weight babies thrive
- Food voucher experiment aims to tackle hunger in the philippines
- Nutrition lessons boost health in vietnamese children
- Can monthly arm measurements save kids from malnutrition?
- Can extra calories help kids with heart disease grow stronger?