RECRUITING

Impact of Serial Bedside Video Calls on Stress Level in Parents of Infants Admitted to NICU

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Impact of Serial Bedside Video Call Communication on Stress Level in Parents of Infants Admitted to NICU.

Quick Facts

Study Start:2024-06-01
Study Completion:2025-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06252883

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:7 Days to 60 Days
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. * intrauterine drug exposure
  2. * major critical congenital cardiac anomaly
  3. * major neurologic anomaly
  4. * chromosomal disorder.

Contacts and Locations

Study Contact

Nanda Vishakha, MD
CONTACT
312-864-6000
vishakha.nanda@cookcountyhhs.org
Ugoeze Otome, MD
CONTACT
ugoeze.otome@cookcountyhealth.org

Principal Investigator

Nanda Vishakha, MD
PRINCIPAL_INVESTIGATOR
John H Stroger Hospital of Cook County, IL

Study Locations (Sites)

John H. Stroger Hospital of Cook County
Chicago, Illinois, 60612
United States

Collaborators and Investigators

Sponsor: Cook County Health

  • Nanda Vishakha, MD, PRINCIPAL_INVESTIGATOR, John H Stroger Hospital of Cook County, IL

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-06-01
Study Completion Date2025-05

Study Record Updates

Study Start Date2024-06-01
Study Completion Date2025-05

Terms related to this study

Keywords Provided by Researchers

  • Parental stress
  • Anxiety
  • NICU
  • PSS-NICU
  • STAI-Y

Additional Relevant MeSH Terms

  • Stress