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Infant Behavioral Sleep Intervention: Comparative Efficacy

Primary Purpose

Insomnia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Bedtime routine
Sleep schedule
Intervention (bedtime)
Intervention (after night wakings)
Sponsored by
Indiana University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Insomnia focused on measuring Infant behavioral sleep intervention, Infant sleep, Pediatric insomnia, Infant night wakings

Eligibility Criteria

6 Months - 18 Months (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Infant has disruptive night wakings (wakes 1x or more/night, 5+ nights per wk; caregiver intervenes at night wakings)
  • Infant is placed in bed asleep in a crib/bassinet or similar at bedtime at least five nights per week
  • Parent/caregiver goal is for the infant to fall asleep independently at bedtime and/or return to sleep independently during the night
  • Parent/caregiver goal is for the infant to sleep in crib or similar
  • Parent/caregiver lives in the home with the infant, is typically at home at the time of the infant's typical bedtime at least 5 nights a week, and is primary caregiver at bedtime and during the night.
  • The family must have in-home private wireless access that they are willing to share with the study team (necessary for streaming video)
  • Families lives in Indianapolis, Indiana or surrounding areas (within 50 miles of Indiana University School of Medicine)

Exclusion Criteria:

  • Infant has a chronic major medical condition that affects sleep
  • Infant has a major developmental condition (e.g. Down syndrome)
  • Family is already receiving professional help for the infant's sleep problems
  • Infant snores 5+ nights per week (in which case a sleep study will be recommended; families could participate in the study following a negative sleep study.)
  • Infant has chronic skin conditions (e.g. eczema) that would prohibit wearing an actigraph on the leg

Sites / Locations

  • Indiana University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Experimental

Experimental

Arm Label

Control

Intervention (Bedtime only)

Intervention (All night)

Arm Description

Infant sleep monitoring and parental surveys only

Infant behavioral sleep intervention implemented at bedtime only. Parents are instructed to soothe/help their infant back to sleep after night wakings. Includes a tailored sleep schedule and bedtime routine, as well as support from a sleep interventionist.

Infant behavioral sleep intervention implemented at bedtime and after each subsequent infant night waking. Includes a tailored sleep schedule and bedtime routine, as well as support from a sleep interventionist.

Outcomes

Primary Outcome Measures

Infant sleep (subjective)
Total score on Infant Sleep Questionnaire (ISQ; range=0-38; higher score indicate more problematic sleep)

Secondary Outcome Measures

Infant sleep (objective): wake after sleep onset
Wake after sleep onset in minutes (assessed via videosomnography)
Infant sleep (subjective): wake after sleep onset
Wake after sleep onset in minutes (assessed via parent report on sleep diary)
Infant sleep (objective): longest sleep period
Longest sleep period in minutes (assessed via videosomnography)
Infant sleep (subjective): longest sleep period
Longest sleep period in minutes (assessed via parent report on sleep diary)
Parental stress
Daily parental rating of nightly stress associated with their infant's sleep
Parental mood
Profile of Mood State - 2nd edition, total score
Parental sleep
Pittsburgh Sleep Quality Index, total score

Full Information

First Posted
February 9, 2018
Last Updated
April 16, 2019
Sponsor
Indiana University
Collaborators
Purdue University, Saint-Joseph University
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1. Study Identification

Unique Protocol Identification Number
NCT03447665
Brief Title
Infant Behavioral Sleep Intervention: Comparative Efficacy
Official Title
Infant Behavioral Sleep Intervention: Comparative Efficacy Across Two Approaches "The Sleeping Baby Study"
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
February 1, 2018 (Actual)
Primary Completion Date
April 10, 2019 (Actual)
Study Completion Date
April 10, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indiana University
Collaborators
Purdue University, Saint-Joseph University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
While frequent night awakenings in newborns are common and expected, an estimated 20-30% of older infants and toddlers have frequent problematic night wakings requiring parental intervention throughout the night. Standard infant behavioral sleep intervention approaches, which require parental intervention throughout the night, are effective but often difficult for families to implement. The aim of this study is to compare the efficacy of two infant behavioral sleep interventions with a no treatment condition, on infant sleep and family functioning. Healthy infants between the ages of 6 and 18 months with night wakings will be randomized into one of three conditions: Entire night intervention, bedtime only intervention, or no treatment.
Detailed Description
Study Design: Randomized controlled trial (RCT). Approximately thirty participants will be randomized to a control condition or one of two intervention conditions. Participants: Participants are healthy infants between the ages of 6 and 18 months who wake during the night, and their parents. Parents must be willing to engage in infant behavioral sleep intervention. Study Procedure: Participant recruitment strategies include direct referrals from community primary care providers (PCP)s, signs posted in medical offices, and social media posts. Participants will be screened and consented via phone. Team members will conduct three home visits with participating families to install videorecording device and actigraphy and take a sleep history (Visit 1); teach families the intervention (Visit 2); and remove monitoring equipment and offer intervention to families in the control condition (Visit 3). Parents will be asked to complete daily sleep logs and three sets of surveys using REDCap. Intervention: The intervention consists of an infant behavioral sleep protocol. For both intervention conditions an interventionist will collaborate with the family to design a tailored sleep schedule and bedtime routine. The interventionist will then teach the family a behavioral approach, which involves placing the infant in his/her crib awake, and leaving the room. The behavioral approach will be individually tailored for each family (e.g., periodic checks). The two intervention conditions differ in regards to the timing of the intervention. In the all night condition, which represents a standard intervention approach, parents are asked to implement the behavioral protocol at bedtime and at subsequent night wakings. In the bedtime only condition, parents are asked to implement the behavioral protocol at bedtime only, and to soothe their infant back to sleep following night wakings. Measures: Infant sleep will be assessed via parent-report (sleep diary and validated measure); actigraphy; and videosomnography. Parent sleep, parent mood, and infant mood will be assessed via validated parental-report survey measures. Collaborators on this study include: AJ Schwichtenberg, Purdue University; Jodi Mindell, Saint Joseph University.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insomnia
Keywords
Infant behavioral sleep intervention, Infant sleep, Pediatric insomnia, Infant night wakings

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Families are randomly assigned to one of three groups: control, bedtime only (intervention), or all night (intervention).
Masking
Outcomes Assessor
Masking Description
The individuals coding videosomnography are blinded to the participant's condition.
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Infant sleep monitoring and parental surveys only
Arm Title
Intervention (Bedtime only)
Arm Type
Experimental
Arm Description
Infant behavioral sleep intervention implemented at bedtime only. Parents are instructed to soothe/help their infant back to sleep after night wakings. Includes a tailored sleep schedule and bedtime routine, as well as support from a sleep interventionist.
Arm Title
Intervention (All night)
Arm Type
Experimental
Arm Description
Infant behavioral sleep intervention implemented at bedtime and after each subsequent infant night waking. Includes a tailored sleep schedule and bedtime routine, as well as support from a sleep interventionist.
Intervention Type
Behavioral
Intervention Name(s)
Bedtime routine
Intervention Description
Tailored bedtime routine
Intervention Type
Behavioral
Intervention Name(s)
Sleep schedule
Intervention Description
Tailored sleep schedule, including morning rise time, cut-off for last nap of the day, and bedtime.
Intervention Type
Behavioral
Intervention Name(s)
Intervention (bedtime)
Intervention Description
Parents implement behavioral sleep intervention at bedtime.
Intervention Type
Behavioral
Intervention Name(s)
Intervention (after night wakings)
Intervention Description
Parents implement behavioral sleep intervention following each night waking.
Primary Outcome Measure Information:
Title
Infant sleep (subjective)
Description
Total score on Infant Sleep Questionnaire (ISQ; range=0-38; higher score indicate more problematic sleep)
Time Frame
Change in score from baseline (day 2, prior to the start of intervention) to post-intervention (day 16)
Secondary Outcome Measure Information:
Title
Infant sleep (objective): wake after sleep onset
Description
Wake after sleep onset in minutes (assessed via videosomnography)
Time Frame
Average per night from nights 1-3 (baseline) compared to average from nights 15-17 (2 weeks later; after intervention)
Title
Infant sleep (subjective): wake after sleep onset
Description
Wake after sleep onset in minutes (assessed via parent report on sleep diary)
Time Frame
Average per night from nights 1-3 (baseline) compared to average from nights 15-17 (2 weeks later; after intervention)
Title
Infant sleep (objective): longest sleep period
Description
Longest sleep period in minutes (assessed via videosomnography)
Time Frame
Average per night from nights 1-3 (baseline) compared to average from nights 15-17 (2 weeks later; after intervention)
Title
Infant sleep (subjective): longest sleep period
Description
Longest sleep period in minutes (assessed via parent report on sleep diary)
Time Frame
Average per night from nights 1-3 (baseline) compared to average from nights 15-17 (2 weeks later; after intervention)
Title
Parental stress
Description
Daily parental rating of nightly stress associated with their infant's sleep
Time Frame
Average from nights 1-3 (baseline) compared to average from nights 15-17 (2 weeks later; after intervention)
Title
Parental mood
Description
Profile of Mood State - 2nd edition, total score
Time Frame
Baseline (day 2, prior to the start of intervention) compared to post-intervention (day 16)
Title
Parental sleep
Description
Pittsburgh Sleep Quality Index, total score
Time Frame
Baseline (day 2, prior to the start of intervention) compared to post-intervention (day 16)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
18 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Infant has disruptive night wakings (wakes 1x or more/night, 5+ nights per wk; caregiver intervenes at night wakings) Infant is placed in bed asleep in a crib/bassinet or similar at bedtime at least five nights per week Parent/caregiver goal is for the infant to fall asleep independently at bedtime and/or return to sleep independently during the night Parent/caregiver goal is for the infant to sleep in crib or similar Parent/caregiver lives in the home with the infant, is typically at home at the time of the infant's typical bedtime at least 5 nights a week, and is primary caregiver at bedtime and during the night. The family must have in-home private wireless access that they are willing to share with the study team (necessary for streaming video) Families lives in Indianapolis, Indiana or surrounding areas (within 50 miles of Indiana University School of Medicine) Exclusion Criteria: Infant has a chronic major medical condition that affects sleep Infant has a major developmental condition (e.g. Down syndrome) Family is already receiving professional help for the infant's sleep problems Infant snores 5+ nights per week (in which case a sleep study will be recommended; families could participate in the study following a negative sleep study.) Infant has chronic skin conditions (e.g. eczema) that would prohibit wearing an actigraph on the leg
Facility Information:
Facility Name
Indiana University School of Medicine
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Infant Behavioral Sleep Intervention: Comparative Efficacy

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