| Methods | Study design: Randomized controlled trial |
| Unit of randomization: Individually randomized | |
| Type of study: Food Program | |
| Participants | Location/setting: Maternal Child Health (MCH) centre, Rajchaburi (100 km from Bangkok),Thailand |
| Population: Not specified | |
| Sample size: 43 | |
| Drop outs/withdrawal: None | |
| Socio‐demographics | |
| Mean (SD) age: | |
| Intervention groups: | |
| I: 22.4 (3.0), | |
| II: 25.0 (4.8) | |
| III: 23.4 (4.5). | |
| Age range: 16‐30 years | |
| Occupation: Not specified | |
| Race: Not specified | |
| Education: Not specified | |
| Family income: Not specified | |
| Inclusion criteria: All nonsmoking women, who ranged in age from 16 to 30 year who attended the MCH centre (local hospital) | |
| Exclusion criteria: Not specified | |
| Interventions | Intervention (sample size): |
| Supplemented groups (I and II): | |
| Group I: received a mix of soybean, mungbean, sesame and sugar coming to, on average, 384 kcal energy, 9.1 g fat and 15 g protein | |
| Group II: received a mix of rice, dried shrimp, groundnut, sugar and oil coming to, on average, 348 kcal energy, 15.6 g fat and 13.1 g protein | |
| The supplement was instructed to be consumed as an additional snack and was initiated from the 28th (±2) week of gestation and stopped at birth | |
| Control (sample size): | |
| Nonsupplemented group (III): | |
| Group III: Did not receive any supplementation | |
| Concomitant interventions: | |
| Each participant's blood haematocrit was determined before delivery | |
| Training: Not specified | |
| Follow‐up: | |
| Subjects visited the MCH centre every 2 weeks until delivery. These visits consisted of General physical and obstetric examination, anthropometric measurement, 24‐h dietary recall and acceptability and consumption patterns of supplementary formula | |
| Outcomes | Primary outcomes: None |
| Secondary outcomes: | |
| Birth weight | |
| Birth length | |
| Head circumference | |
| Timing of outcome assessment: Every newborn was weighed without clothes within 30 min after delivery | |
| Notes | Study start date: Not specified |
| Study end date: Not specified | |
| Time period: Not specified | |
| Study country: Thailand | |
| Study limitations: Not specified | |
| Funding source: The project funded by the research committee of the Faculty of Medicine, Ramathibodi Hospital, Mahidol University | |
| Conflict of interest: Not specified |