Sleep-Safe: A Strong African American Families Study
Primary Purpose
Weight Gain
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Sleep Soothe
Sleep Safe
Sponsored by
About this trial
This is an interventional prevention trial for Weight Gain focused on measuring Responsive parenting, Mother-child relations, Infant feeding, Infant sleeping, Infant obesity
Eligibility Criteria
Inclusion Criteria:
- Infant > 37 0/7 weeks gestational age, apparently healthy and without significant morbidity
- Singleton infant
- Nursery/NICU/maternity stay of 7 days or less
- Mother at least 17 years of age
- Mother self-identifies as African American
- Mother is primiparous
Exclusion Criteria:
- Non-English speaking
- Infant birth weight <2500 grams
- Presence of a congenital anomaly or neonatal physical or metabolic condition that significantly affects a newborn's feeding (e.g. cleft lip, cleft palate, metabolic disease)
- Any major maternal morbidities, pre-existing condition that would affect postpartum care or her ability to care for her newborn (e.g., narcotic drug use: heroin, cocaine, meth, pain pills, etc; on chemotherapy; uncontrolled MS; uncontrolled depression causing social service contact).
- Plan for newborn to be adopted
- Plan to move from area within four months of delivery
- Residence further than 75 miles from Augusta, GA
Sites / Locations
- University of Georgia
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Sleep Soothe
Sleep Safe
Arm Description
An intervention in which parents are given information on how to respond to their baby's cues related to sleeping and fussiness.
An intervention in which parents are given information on a safe sleep environment, as well as other strategies to keep baby safe
Outcomes
Primary Outcome Measures
Change in infants' weight for age from 3 weeks to 16 weeks (conditional weight gain)
Standardized residuals from the linear regression of weight for age at 16 weeks on weight for age at 3 weeks, with length for age at birth and 16 weeks and infant age at the 16-week assessment entered as covariates
Secondary Outcome Measures
Change in infants' weight for age
Growth curve models of change in infants' weight for age
Weight-for-age z scores
Weight-for-age z scores at 16 weeks
Weight-for-length z scores
Weight-for-length z scores at 16 weeks
Infant BMI z scores
BMI z scores at 16 weeks
Full Information
NCT ID
NCT03505203
First Posted
April 3, 2018
Last Updated
October 26, 2022
Sponsor
University of Georgia
Collaborators
Augusta University, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
1. Study Identification
Unique Protocol Identification Number
NCT03505203
Brief Title
Sleep-Safe: A Strong African American Families Study
Official Title
Sleep-Safe: A Strong African American Families Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
March 4, 2018 (Actual)
Primary Completion Date
July 5, 2021 (Actual)
Study Completion Date
July 5, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Georgia
Collaborators
Augusta University, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Rapid weight gain during infancy is a powerful, and potentially malleable, risk factor for later overweight and obesity, but limited research has examined the impact of promising interventions when applied to the groups most at risk for rapid weight gain in infancy. The present study examines whether providing mothers of newborns with responsive parenting guidance during the first weeks of life to promote infant sleep and soothing can reduce rapid weight gain for African American infants born in low SES contexts.
Detailed Description
The study design is a randomized controlled trial. This trial will deliver a responsive parenting intervention (Sleep Soothe) to provide information on how to soothe, how to distinguish hunger from other distress, how to promote self-soothing, and bedtime routines. The responsive parenting intervention will be compared to a safety control group (Sleep Safe). The programs will be delivered across 2 sessions at 3-weeks and 8-weeks postpartum. Both interventions and all data collection will be delivered in participants' homes. Assessments will be conducted in participants' homes at 1-week postpartum, 3 weeks postpartum, 8 weeks postpartum, and 16-weeks postpartum.
Three hundred African American infants and their mothers will be recruited from the mother/baby nursery at Augusta University Medical Center. A dedicated recruitment coordinator will have access to electronic medical records systems in order to pre-screen mothers and infants. The recruitment coordinator will approach those who match basic inclusion criteria and will deliver an approved verbal script to pre-screened mothers to determine interest in participation. Interested mothers will respond to remaining screening questions in order to confirm eligibility. Once enrollment criteria are satisfied, informed consent will be obtained from the infant's mother during her hospital stay. Mothers will also complete selected demographic information. Anthropometric measurements will be obtained on the infant, mother, and father (optional). After enrollment, families will be scheduled for a research visit at their home at 1 week postpartum.
At home visit 1 (7-10 days postpartum), mothers (and fathers, if interested) will complete questionnaire measures using Qualtrics. There will also be measurements of infant weight and length. Families will be randomized to condition following this visit.
At home visit 2 (3 weeks postpartum), families will receive either the responsive parenting intervention or the safety control intervention. They will complete brief questionnaires. Measures of infant, maternal, and paternal (optional) weight will be obtained.
At home visit 3 (8 weeks postpartum), families will receive either the second part of the responsive parenting intervention or the second part of the safety control intervention. They will complete brief questionnaires. Measures of infant, maternal, and (optional: paternal) weight will be obtained. Mothers will be provided with activity monitors for themselves and for their babies that will be picked up by study staff after 7 days' use.
At home visit 4 (16 weeks postpartum), mothers will complete questionnaire measures (fathers' participation is optional). Measures of maternal and paternal (optional) weight will be obtained, as will measures of infant weight, length, and head circumference.
We test the following specific aims:
Specific Aim 1: To assess the effects of responsive parenting, focused on infant sleep and soothing, on reducing rapid weight gain from 3 to 16 weeks among African American infants. We hypothesize that infants in the Sleep Soothe condition will gain weight more slowly compared to infants in the Sleep Safe condition and have lower weight outcomes (i.e., BMI z scores, weight-for-length z scores, weight-for-age z scores) at age 16 weeks.
Specific Aim 2: To assess effects of responsive parenting on parental and infant behaviors. We hypothesize that compared with parents in the Sleep Safe condition, parents in the Sleep Soothe condition will show increases in responsive parenting, parenting self-efficacy, and the use of alternatives to feeding to soothe (white noise, pacifier, etc.), and decreases in feeding to soothe. Over time, infants in this condition will have longer sleep bouts and fewer feedings.
Specific Aim 3: To examine moderation of intervention effects by individual and contextual factors.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Weight Gain
Keywords
Responsive parenting, Mother-child relations, Infant feeding, Infant sleeping, Infant obesity
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be assigned to one of two conditions: (1) Sleep Soothe (responsive parenting), where parents are given information on how to respond to their baby's cues related to sleeping and fussiness, and (2) Sleep Safe (safety control), where parents are given information on a safe sleep environment, as well as other strategies they can use to keep their baby safe.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
234 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sleep Soothe
Arm Type
Experimental
Arm Description
An intervention in which parents are given information on how to respond to their baby's cues related to sleeping and fussiness.
Arm Title
Sleep Safe
Arm Type
Active Comparator
Arm Description
An intervention in which parents are given information on a safe sleep environment, as well as other strategies to keep baby safe
Intervention Type
Behavioral
Intervention Name(s)
Sleep Soothe
Intervention Description
An intervention in which parents are given information on how to respond to their baby's cues related to sleeping and fussiness.
Intervention Type
Behavioral
Intervention Name(s)
Sleep Safe
Intervention Description
An intervention in which parents are given information on a safe sleep environment, as well as other strategies to keep baby safe.
Primary Outcome Measure Information:
Title
Change in infants' weight for age from 3 weeks to 16 weeks (conditional weight gain)
Description
Standardized residuals from the linear regression of weight for age at 16 weeks on weight for age at 3 weeks, with length for age at birth and 16 weeks and infant age at the 16-week assessment entered as covariates
Time Frame
3 weeks to 16 weeks
Secondary Outcome Measure Information:
Title
Change in infants' weight for age
Description
Growth curve models of change in infants' weight for age
Time Frame
3 weeks to 16 weeks
Title
Weight-for-age z scores
Description
Weight-for-age z scores at 16 weeks
Time Frame
16 weeks
Title
Weight-for-length z scores
Description
Weight-for-length z scores at 16 weeks
Time Frame
16 weeks
Title
Infant BMI z scores
Description
BMI z scores at 16 weeks
Time Frame
16 weeks
Other Pre-specified Outcome Measures:
Title
Maternal report of infant sleep at 8 weeks
Description
Sleep duration and number of night awakenings using the Brief Infant Sleep Questionnaire (Sadeh, 2004)
Time Frame
8 weeks
Title
Maternal report of infant sleep at 16 weeks
Description
Sleep duration and number of night awakenings using the Brief Infant Sleep Questionnaire (Sadeh, 2004)
Time Frame
16 weeks
Title
Maternal sleep actigraphy
Description
7-day actigraphy data to assess mothers' sleep duration
Time Frame
8 weeks postpartum
Title
Infant soothing at 8 weeks
Description
Parents use feeding for reasons other than in response to hunger
Time Frame
8 weeks
Title
Infant soothing at 16 weeks
Description
Parents use feeding for reasons other than in response to hunger
Time Frame
16 weeks
Title
Infant feeding frequency at 16 weeks
Description
Feeding frequency, use of bottle feeding, and introduction of solids using Babies Need Feeding (Stifter et al., 2011)
Time Frame
16 weeks
Title
Safe sleep practices
Description
Frequency of sleep safety practices (Fowler et al., 2013)
Time Frame
16 weeks
Title
Child safety practices
Description
Child safety practices assessed using the Framingham Safety Survey (Hansen et al., 1996)
Time Frame
16 weeks
Title
Infant eating behavior
Description
Infant eating behavior using the Baby Eating Behavior Questionnaire (Llewellyn et al., 2011)
Time Frame
16 weeks
Title
Parental self-efficacy at 8 weeks
Description
Perceived parental self-efficacy at 8 weeks using total score from the Karitane Parenting Confidence Scale (Crncec, Barnett, & Matthey, 2008)
Time Frame
8 weeks
Title
Parental self-efficacy at 16 weeks
Description
Perceived parental self-efficacy at 16 weeks using total score from the Karitane Parenting Confidence Scale (Crncec, Barnett, & Matthey, 2008)
Time Frame
16 weeks
Title
Maternal feeding practices and beliefs at 8 weeks
Description
Maternal feeding beliefs and behaviors using the Infant Feeding Styles Questionnaire (Thompson et al., 2009)
Time Frame
8 weeks
Title
Maternal feeding practices and beliefs at 16 weeks
Description
Maternal feeding beliefs and behaviors using the Infant Feeding Styles Questionnaire (Thompson et al., 2009)
Time Frame
16 weeks
Title
Maternal depressive symptoms at 8 weeks
Description
Maternal depressive symptoms at 8 weeks using the CES-D (Radloff, 1977)
Time Frame
8 weeks
Title
Maternal depressive symptoms at 16 weeks
Description
Maternal depressive symptoms at 16 weeks using the CES-D (Radloff, 1977)
Time Frame
16 weeks
Title
Family routines
Description
Extent to which there is order and routine versus chaos and confusion in their home. Uses total score from the Confusion, Hubbub, and Order Scale (Matheny et al., 1995)
Time Frame
8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Infant > 37 0/7 weeks gestational age, apparently healthy and without significant morbidity
Singleton infant
Nursery/NICU/maternity stay of 7 days or less
Mother at least 17 years of age
Mother self-identifies as African American
Mother is primiparous
Exclusion Criteria:
Non-English speaking
Infant birth weight <2500 grams
Presence of a congenital anomaly or neonatal physical or metabolic condition that significantly affects a newborn's feeding (e.g. cleft lip, cleft palate, metabolic disease)
Any major maternal morbidities, pre-existing condition that would affect postpartum care or her ability to care for her newborn (e.g., narcotic drug use: heroin, cocaine, meth, pain pills, etc; on chemotherapy; uncontrolled MS; uncontrolled depression causing social service contact).
Plan for newborn to be adopted
Plan to move from area within four months of delivery
Residence further than 75 miles from Augusta, GA
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Justin A Lavner, Ph.D.
Organizational Affiliation
University of Georgia
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Georgia
City
Athens
State/Province
Georgia
ZIP/Postal Code
30602
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
35684150
Citation
Moore AM, Smith JJ, Stansfield BK, Savage JS, Lavner JA. Patterns and Predictors of Breast Milk Feeding from Birth to Age 4 Months among Primiparous African American Mother-Infant Dyads. Nutrients. 2022 Jun 4;14(11):2350. doi: 10.3390/nu14112350.
Results Reference
background
PubMed Identifier
31277694
Citation
Lavner JA, Stansfield BK, Beach SRH, Brody GH, Birch LL. Sleep SAAF: a responsive parenting intervention to prevent excessive weight gain and obesity among African American infants. BMC Pediatr. 2019 Jul 5;19(1):224. doi: 10.1186/s12887-019-1583-7.
Results Reference
background
PubMed Identifier
35577176
Citation
Lavner JA, Savage JS, Stansfield BK, Beach SRH, Marini ME, Smith JJ, Sperr MC, Anderson TN, Hernandez E, Moore AM, Caldwell AL, Birch LL. Effects of the Sleep SAAF responsive parenting intervention on rapid infant weight gain: A randomized clinical trial of African American families. Appetite. 2022 May 13;175:106080. doi: 10.1016/j.appet.2022.106080. Online ahead of print.
Results Reference
result
PubMed Identifier
36183135
Citation
Hernandez E, Lavner JA, Moore AM, Stansfield BK, Beach SRH, Smith JJ, Savage JS. Sleep SAAF responsive parenting intervention improves mothers' feeding practices: a randomized controlled trial among African American mother-infant dyads. Int J Behav Nutr Phys Act. 2022 Oct 1;19(1):129. doi: 10.1186/s12966-022-01366-1.
Results Reference
result
Learn more about this trial
Sleep-Safe: A Strong African American Families Study
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