CompletedNot Applicable

The Effectiveness of HBM-based Education Program on Improve Knowledge and Behaviors

Taiwan80 participantsStarted 2022-09-10

Plain-language summary

The randomized controlled trial design with one intervention arm (nutrition education and complementary feeding) and one control (usual care) arm (1:1 ratio). Randomization of each participant to the groups will be carried out using Random Allocation Software 1.0 (https://random-allocation-oftware.software.informer.com/1.0/) to intervention or control groups in a 1:1 ratio. The sample size to be recruited is 80 participants.

Who can participate

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Mothers who have children under 2 years of ages with undernutrition categories residences in Lombok Barat or Lombok Tengah District, * Mothers who are able to speak Bahasa or Sasak languages, * Mothers who are able to use a telephone. Exclusion Criteria: * Mothers with impaired cognitive function, and psychiatric diseases, * Children suffering from severe/chronic diseases, mental retardation, physical disability, * Children with hospitalization within six months.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Knowledge of Undernutrition

Timeframe: before intervention

Knowledge of Undernutrition

Timeframe: at two weeks after intervention

Complementary Feeding Practice

Timeframe: before intervention

Complementary Feeding Practice

Timeframe: at two weeks after intervention

Self-efficacy

Timeframe: before intervention

Self-efficacy

Timeframe: at two weeks after intervention

Trial details

NCT IDNCT05517395

SponsorTaipei Medical University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-12-30

View on ClinicalTrials.gov More Undernutrition trials

Plain-language summary

Who can participate

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Knowledge of Undernutrition

Timeframe: before intervention

Knowledge of Undernutrition

Timeframe: at two weeks after intervention

Complementary Feeding Practice

Timeframe: before intervention

Complementary Feeding Practice

Timeframe: at two weeks after intervention

Self-efficacy

Timeframe: before intervention

Self-efficacy

Timeframe: at two weeks after intervention