School of Human Sciences, Faculty of Education, Health and Human Sciences, University of Greenwich, Park Row, London SE10 9 LS, UK.
Nutritional Epidemiology Observatory, Department of Social and Applied Nutrition, Institute of Nutrition Josué de Castro, Federal University of Rio de Janeiro, 21941-902 Rio de Janeiro, Brazil.
Int J Environ Res Public Health. 2020 Oct 30;17(21):8023. doi: 10.3390/ijerph17218023.
This study aims to assess the acceptability, adherence, and retention of a feasibility trial on milk fortification with calcium and vitamin D (Ca+VitD) and periodontal therapy (PT) among low income Brazilian pregnant women with periodontitis (IMPROVE trial). This 2 × 2 factorial feasibility trial used a mixed-methods evaluation. In total, 69 pregnant women were randomly allocated to four groups: 1. fortified sachet with Ca+VitD and milk plus early PT (throughout gestation); 2. placebo and milk plus early PT; 3. fortified sachet with Ca+VitD and milk plus late PT after childbirth; 4. placebo and milk plus late PT. Data were collected via questionnaires, field notes, participant flow logs, treatment diary, and focal group discussions. Quantitative and qualitative data were analysed using appropriate descriptive statistics and content analysis, respectively. Eligibility rate (12%) was below the target of 15%, but participation (76.1%) and recruitment rate (2 women/week) exceeded the targets. Retention rate (78.6%) was slightly below the target (80%). Adherence to the PT was significantly higher in the early treatment groups (98.8%) compared to the late treatment groups (29%). All women accepted the random allocation, and baseline groups were balanced. There was no report of adverse events. This multi-component intervention is acceptable, well-tolerated, and feasible among low-risk pregnant women in Brazil.
本研究旨在评估一项针对巴西低收入牙周炎孕妇的可行性试验,即钙和维生素 D(Ca+VitD)强化牛奶和牙周治疗(PT)的可接受性、依从性和保留率(IMPROVE 试验)。这是一项 2×2 析因可行性试验,采用混合方法评估。共有 69 名孕妇被随机分配到四个组:1. 强化钙和维生素 D 袋与牛奶加早期 PT(整个孕期);2. 安慰剂和牛奶加早期 PT;3. 强化钙和维生素 D 袋与牛奶加产后晚期 PT;4. 安慰剂和牛奶加产后晚期 PT。通过问卷、现场记录、参与者流程日志、治疗日记和焦点小组讨论收集数据。使用适当的描述性统计和内容分析分别对定量和定性数据进行分析。合格率(12%)低于目标的 15%,但参与率(76.1%)和招募率(每周 2 名妇女)超过了目标。保留率(78.6%)略低于目标(80%)。早期治疗组的 PT 依从性明显高于晚期治疗组(98.8%对 29%)。所有妇女均接受了随机分组,基线组平衡。没有报告不良事件。这种多成分干预措施在巴西低风险孕妇中是可接受的、耐受良好且可行的。