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临床试验/NCT03664154
NCT03664154已完成不适用

Stress and Feeding (SAFE): A Pilot Intervention for Mothers and Their Preterm Infants

Virginia Commonwealth University2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2019年5月15日最近更新:
适应症

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

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)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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