- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04373915
Evaluating Parent Engagement, Attachment, Stress, and Satisfaction With Remote Rounding in the NICU
Improving Family Engagement With Remote Rounding in the NICU
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Every year 10 to 15 percent of infants born in the United States, totaling roughly half a million babies, are admitted to a Neonatal Intensive Care Unit (NICU). Although survival rates are generally high, as many as half of these infants require a prolonged hospital stay. For parents, the admission of a newborn to the NICU is among the most emotionally distressing situations that they can face. A prolonged hospital stay can further impact the mother and family physically, psychologically, and financially.
During admission in the NICU it is often difficult for families to be present at bedside rounds on a daily basis due to transportation challenges or competing demands of work and care for siblings. Conflicting schedules between families and doctors make it more difficult to discuss and collaborate with families in the care of their child. The investigators hypothesize that this deficiency of communication and perceived loss of control can have significant impacts on maternal stress, satisfaction, engagement, and attachment.
Outside of the medical field, technology continues to advance as rapidly as ever. The medical field continues to struggle with adapting and using new technology and continue to lag behind many other fields. In recent years telemedicine has been used to facilitate patient care delivery, improve accessibility of health care services, and reduce healthcare costs however this use remains largely in the outpatient sector.
In the Neonatal Intensive Care Unit, Telemedicine has been used by one group to improve parent satisfaction in a variety of areas. A pilot study of the concept of remote or virtual rounding in a Pediatric Intensive Care Unit has been recently published in the literature. This project seeks to expand upon this knowledge to define and measure the impact on several aspects of neonatal care.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ohio
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Cleveland, Ohio, United States, 44106
- Rainbow Babies and Children's Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Parents with an infant admitted to the NICU/R4 with an anticipated length of stay of 2 weeks or more
- Parent consents to study and answering questionnaires
- English speaking
- Infant is assigned to red or purple medical service team.
- Infant age at enrollment: zero to 14 days old
Exclusion Criteria:
- Parents with an infant admitted to the NICU/R4 with an anticipated length of stay less than 2 weeks
- Parent is not willing to answer questionnaires
- Non-English speaking
- Patient is not assigned to red or purple medical service team.
- Discharge to other than biological parents expected
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Standard Bedside Rounding
|
|
|
Experimental: Remote Bedside Rounding
Parents of infants on one care team will have the opportunity to participate in rounds via secure remote video software.
|
Parents of infants on the medical team utilizing remote rounding will have the opportunity to participate in rounds by video conferencing at the infant's bedside.
Participation will be tracked and surveys regarding stress, satisfaction, and attachment will be completed by parents in both groups.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parent Engagement
Time Frame: up to 1 year.
|
Calendars will be placed at each infant's bedside to record engagement events consisting of participation in rounds, phone calls, visits, and kangaroo care.
Each parental interaction recorded on the calendar will be counted.
The mean and standard deviation of interactions over the study period will be calculated for each arm.
|
up to 1 year.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parent Satisfaction: survey
Time Frame: up to 6-10 weeks
|
A short investigator created satisfaction survey will be used to measure parent satisfaction.
Each question on the parent satisfaction survey will be analyzed separately and compared between the two groups.
A Mann-Whitney U test will be used for each of the 8 likert questions.
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up to 6-10 weeks
|
|
Parent Stress
Time Frame: up to 6-10 weeks
|
The Parental Stressor Scale: Neonatal Intensive Care Unit (PSS:NICU) will be used to measure parent stress.
The instrument is a 46-item scale with 3 sub scales: infant behavior and appearance, parental role alteration, and sights and sounds.
Each item is scored 1-5 on a likert scale (total sore range 46-230) with higher scores relating to higher stress.
A standard t-test will be used.
|
up to 6-10 weeks
|
|
Parent Attachment survey
Time Frame: up to 6-10 weeks
|
The Maternal Attachment Inventory will be used to measure parent-infant attachment.
This is a 26 item scale with each item scoring 1-4, for a total possible score of 26-104 with a higher score showing better attachment.
Differences in attachment between the two arms will be assessed using a Wilcoxon rank sum test.
|
up to 6-10 weeks
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Margaret Kuper-Sasse, MD, Rainbow Babies and Children's Hospital
Publications and helpful links
General Publications
- Muller ME. A questionnaire to measure mother-to-infant attachment. J Nurs Meas. 1994 Winter;2(2):129-41.
- Miles MS, Funk SG, Carlson J. Parental Stressor Scale: neonatal intensive care unit. Nurs Res. 1993 May-Jun;42(3):148-52.
- Gray JE, Safran C, Davis RB, Pompilio-Weitzner G, Stewart JE, Zaccagnini L, Pursley D. Baby CareLink: using the internet and telemedicine to improve care for high-risk infants. Pediatrics. 2000 Dec;106(6):1318-24. doi: 10.1542/peds.106.6.1318.
- Epstein EG, Sherman J, Blackman A, Sinkin RA. Testing the Feasibility of Skype and FaceTime Updates With Parents in the Neonatal Intensive Care Unit. Am J Crit Care. 2015 Jul;24(4):290-6. doi: 10.4037/ajcc2015828.
- Yager PH, Clark M, Cummings BM, Noviski N. Parent Participation in Pediatric Intensive Care Unit Rounds via Telemedicine: Feasibility and Impact. J Pediatr. 2017 Jun;185:181-186.e3. doi: 10.1016/j.jpeds.2017.02.054. Epub 2017 Mar 28.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- STUDY20181178
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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