Using Smartphones in the Neonatal Intensive Care Unit

Status Completed

Clinical Trial Summary

The goal of this research is to develop and pilot the NICU-2-Home service, a health information technology (IT) concept centered on a smart phone app. NICU-2-Home will provide support to parents of very low birth weight (VLBW) infants as they transition from the NICU to their homes and eventually establish a medical home with the infant's pediatrician. Once the app is developed, we will conduct a feasibility study with randomization to pilot test the ability of NICU-2-Home app to (a) improve parent's self-efficacy and confidence in caring for their VLBW infant, (b) decrease parental stress, and (c) enhance involvement with their VLBW infants compared to controls.

Clinical Trial Description

After 2-3 months in the Neonatal Intensive Care Unit (NICU), mothers and fathers of Very Low Birth Weight (VLBW) infants face discharge home with trepidation. Having a VLBW infant that has survived to discharge, these parents now must perform a myriad of health care tasks once at home, yet parents often feel ill-prepared, uninformed, and unskilled to provide this care. The goal of this exploratory research is to develop and pilot the NICU-2-Home service, a health information technology (IT) concept centered on the smart phone that will be created with researchers at Motorola. NICU-2-Home will provide support to parents of VLBW infants as they transition from the NICU to their homes and eventually establish a medical home with the infant's pediatrician. Phase 1 of this research uses qualitative methods and an iterative process to design the NICU-2-Home content service that will support parents as they transition to home from the NICU through interviews with the major stakeholders: parents, neonatal physicians, neonatal staff, and community pediatricians. Phase 2 evaluates NICU-2-Home as parents are transitioning to home and includes a feasibility study with randomization to pilot test the ability of NICU-2-Home to (a) improve parent's self-efficacy and confidence in caring for their VLBW infant, (b) decrease parental stress, and (c) enhance involvement with their VLBW infants compared to controls. ;

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Self-efficacy

Clinical Trial Details

NCT number	NCT01987180
Study type	Observational
Source	Northwestern University
Contact
Status	Completed
Phase	N/A
Start date	January 2013
Completion date	June 2015

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT02906306` - Effects of Individual and Group Occupational Therapy on General Self-Efficacy, Psychological Well-Being, Personal Independence and Occupational Therapy in Older Adults	N/A
Completed	`NCT05562245` - Motivational Interviewing-Based Breastfeeding Education	N/A
Completed	`NCT05576545` - Develop and Evaluate the Effectiveness of a Self-Care Smartphone Application on the Self-Efficacy, and Resilience Among Newly Diagnosed Breast Cancer Patients Undergoing Treatment	N/A
Completed	`NCT03261700` - Recovering From Intimate Partner Violence Through Strengths and Empowerment (RISE)	N/A
Completed	`NCT01001286` - Questscope Non-Formal Education Impact Study	Phase 2
Completed	`NCT02100215` - Quantifying the Influence of Expert Modeling	N/A
Completed	`NCT01672437` - NewPreBP: Project Newborn -Preparation for Birth and Parenthood	N/A
Completed	`NCT01837888` - WheelSee Feasibility Study	N/A
Completed	`NCT00888953` - Nursing Homes Study of Fall Risk Assessment Oriented to Intervention	N/A
Enrolling by invitation	`NCT06339333` - Evaluation of ACT Now GAIN Later	N/A
Completed	`NCT01838135` - WheelSeeU Feasibility Study	N/A
Completed	`NCT06296654` - Effect of Empowerment-Based Interventions on Self-Efficacy and Self-Care Capacity Among Adults With Sickle Cell Disease	N/A
Completed	`NCT05054205` - Motivational Interview-based Self-management Training	N/A
Not yet recruiting	`NCT05863650` - The Effect of Digital-Based Simulation on Physiotherapy Students	N/A
Completed	`NCT04438356` - M-Health Care for Patients After AMI on Disease Perception, Self-Efficacy, Anxiety and Cardio-Respiratory Fitness	N/A
Completed	`NCT02770898` - Improving Family Holistic Health in Probationers	N/A
Completed	`NCT01385241` - Feasibility of a Stigma Reduction Intervention for Human Immunodeficiency Virus (HIV)-Infected Women	N/A
Completed	`NCT06000878` - Evaluate the Effectiveness of First Aid E-book Intervention Among New Nurses	N/A
Not yet recruiting	`NCT05935111` - Physical Activity: Feasibility Study	N/A
Completed	`NCT00145834` - Early Breastfeeding Cessation - is It Possible to Prevent?	Phase 1

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.