Stress and Feeding (SAFE): A Pilot Intervention for Mothers and Their Preterm Infants
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 10
- 试验地点
- 2
- 主要终点
- Ease of recruitment of participants
研究概览
简要总结
A majority of mothers experience high stress levels and associated symptoms of anxiety, depressive symptoms, and sleep disruption during the NICU hospitalization and continuing after hospital discharge. Given preterm infant feeding is one of the most stressful things the new mother will face and given the harmful nature of stress on maternal and infant health, it is important an intervention focuses on both of these concerns: infant feeding and maternal stress. Therefore, the purpose of this research study is two-fold. First, the investigators will examine how practical and acceptable it is for mothers of preterm infants to participate in Stress And FEeding (SAFE) intervention and collect biological stress measures from mothers and their preterm infant's saliva (spit). The intervention is designed to reduce stress and improve maternal feeding interaction. The second purpose of this study is to examine changes before and after using the intervention on mother and infant outcomes over 16-weeks.
详细描述
Descriptive statistics will be computed for demographic and outcome variables. The number of mother/infant dyads recruited but not enrolled will be tracked. If provided, reasons for non-participation will be noted. Enrolled dyads will be tracked and monitored for the number of times the interventions are used and completeness of study data. Acceptability and burden will be assessed by theme analysis of the responses to the interview by the mPI's using traditional strategies of reading and re-reading the transcripts, coding participant responses using their language, and developing categories and subcategories to create a structure for considering acceptability will be completed.. Finally, perceptions of usefulness and satisfaction of the mothers will be assessed by looking at frequencies of Likert responses.
Means and standard errors of the maternal stress and feeding behavior variables will be estimated and graphed across the data collection time points. Although the sample size is small, it is anticipated the mixed effects linear model will be used to assess and quantify changes across time. This model will include a random effect for participant and a fixed effect for time. The model is flexible enough to model potential cofactors, such as age at birth. The study will track the number of successfully obtained, transported, processed and stored samples and compare those number to the proposed maternal and infant cortisol collections.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 60 Years(Adult)
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •English-speaking and reading
- •Given birth to preterm infant < 35-weeks gestation
- •Has access to internet
- •Lives within 50-mile radius of hospital
- •Infant Inclusion Criteria:
- •Born less than 35 week gestation
- •No congenital anomalies that could interfere with feeding (e.g., diaphragmatic hernia, cleft lip/palate tracheoesophageal fistula, and cardiac anomalies
排除标准
- •Chronic neuroendocrine or immunologic condition
- •Currently using guided imagery or other mind-body techniques such as meditation
- •Psychiatric disorder involving a history of dissociative disorders, borderline personalities, and psychotic pathology
- •Infant Exclusion Criteria:
- •Grade III or IV intraventricular hemorrhage
- •Surgical necrotizing enterocolitis
结局指标
主要结局
Ease of recruitment of participants
时间窗: 12-months after study opens to enrollment
Number of mother-infant dyads recruited, with a goal of 15
Track non-participation
时间窗: 16-weeks after start of intervention
Track reasons for non-participation via self-report
Appraisal of SAFE's degree of inconvenience
时间窗: 16-weeks after start of intervention
The participants appraisal of inconvenience will be measured through a semi-structured interview and will be described qualitatively
Satisfaction with intervention
时间窗: 16-weeks after start of intervention
The participants satisfaction with the intervention will be measured using a 26-item Likert scale where 1 represents being not at all satisfied to 5 being very much satisfied.
Adherence
时间窗: 16-weeks after start of intervention
Adherence will be assessed by tracking the number of times the interventions are used
Data collection completeness
时间窗: 16-weeks after start of intervention
Percent of participants with complete data collection at end of study, with a goal of \>75% of patients
次要结局
- Changes in mother biological stress(Baseline to 16-weeks post-baseline)
- Changes in mother-infant feeding behaviors(Baseline to 16-weeks post-baseline)
- Changes in infant biological stress(Baseline to 16-weeks post-baseline)
- Change in maternal stress(Baseline to 16-weeks post-baseline)
