RECRUITING

Bilateral Infant Stimulation Study

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

This study will investigate stress that parents of children admitted to the neonatal intensive care unit (NICU) experience. Investigation of a novel intervention of using bilateral alternating stimulation to reduce parental stress and anxiety and increase bonding/attachment in NICU. Evaluate parental stress and feelings of bonding using surveys before and after the intervention. Intervention will be done at neonate's bedside while admitted to the NICU. Vital sign data will be collected as a marker of parent and neonate's stress response during the intervention.

Official Title

Pilot of the Bilateral Infant Stimulation Study (BLISS): A Parent Provided Positive-Touch Intervention Targeting Stress in the Neonatal Intensive Care Unity (NICU)

Quick Facts

Study Start:2024-02-26
Study Completion:2024-08
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06353243

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:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * admitted to the NICU at the time of study
  2. * greater than 34 weeks gestational age and less than 43 weeks gestational age
  3. * within 4 weeks of admission to NICU at time of initial contact
  4. * have parent or legal guardian willing and able to participate in the study
  1. * those who are less than 3 days postop from surgical procedures
  2. * current use of psychotropic medications or medications that affect the central nervous system (CNS)
  3. * CNS anomaly.

Contacts and Locations

Study Contact

Emily Garavatti
CONTACT
5034942634
garavatt@ohsu.edu

Study Locations (Sites)

Oregon Health and Science University Neonatal Intensive Care Unit
Portland, Oregon, 97219
United States

Collaborators and Investigators

Sponsor: Oregon Health and Science University

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 Date2024-02-26
Study Completion Date2024-08

Study Record Updates

Study Start Date2024-02-26
Study Completion Date2024-08

Terms related to this study

Keywords Provided by Researchers

  • neonates
  • heart rate variability
  • bilateral stimulation
  • positive touch
  • NICU

Additional Relevant MeSH Terms

  • Parent-Child Relations
  • Preterm Birth
  • Stress Reaction
  • Hospitalism in Children