Actively Recruiting
Impact of Serial Bedside Video Calls on Stress Level in Parents of Infants Admitted to NICU
Led by Cook County Health · Updated on 2024-07-24
70
Participants Needed
1
Research Sites
47 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this randomized prospective interventional study is to determine if serial bedside video calls w/audio feature to NICU parents in addition to the routine phone and/or bedside updates can reduce parental stress level. The main question it aims to answer is if the impact of audio-visual calls to nicu parents can improve parent-infant relationship in the form of reduced parental anxiety/stress level. Participants will be parents of infants admitted to NICU for more than seven (7) days. Parents in Group A will receive serial video call communication, 2-3 days a week in addition to the daily phone and/or bedside updates. Parents in Group B will receive daily phone and/or bedside updates per our NICU routine. Parents will complete a series of questionnaires (PSS-NICU, STAI Y-1 \& 2 and MSPSS) at 3 designated periods during an 8-week time frame. Researchers will compare Group A (intervention group) and Group B (control group) to see if there is any difference in the stress levels in relation to the intervention (serial video calls) at the end of the study time frame.
CONDITIONS
Official Title
Impact of Serial Bedside Video Calls on Stress Level in Parents of Infants Admitted to NICU
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Newborns with 7 days or more of NICU stay
You will not qualify if you...
- Infant with intrauterine drug exposure
- Infant with major critical congenital cardiac anomaly
- Infant with major neurologic anomaly
- Infant with chromosomal disorder
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
John H. Stroger Hospital of Cook County
Chicago, Illinois, United States, 60612
Actively Recruiting
Research Team
N
Nanda Vishakha, MD
CONTACT
U
Ugoeze Otome, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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