Multimedia Based Information to Parents in a Pediatric Acute Ward: A Randomized Controlled Trial

This study has been completed.
Sponsor:
Collaborator:
St. Olavs Hospital
Information provided by (Responsible Party):
Norwegian University of Science and Technology
ClinicalTrials.gov Identifier:
NCT01659879
First received: August 2, 2012
Last updated: August 3, 2012
Last verified: August 2012
  Purpose

The aim of this study is to determine whether multimedia based health information presented in a pediatric acute ward to parents of children with breathing difficulties due to lower respiratory tract infections, is more effective than verbal information to reduce the parent's anxiety and to increase satisfaction with nursing care and health information.


Condition Intervention
Health Communication
Behavioral: Multimedia information
Behavioral: verbal information

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Health Services Research
Official Title: Multimedia Based Information to Parents in a Pediatric Acute Ward: A Randomized Controlled Trial

Resource links provided by NLM:


Further study details as provided by Norwegian University of Science and Technology:

Primary Outcome Measures:
  • parental anxiety [ Time Frame: at discharge from the acute ward. An average stay in the acute ward is about 5 hours. ] [ Designated as safety issue: No ]
    evaluated with the State-Trait Anxiety Inventory (STAI) (translated to Norwegian)


Secondary Outcome Measures:
  • parental satisfaction with nursing care [ Time Frame: at discharge from the acute ward. An average stay in the acute ward is about 5 hours. ] [ Designated as safety issue: No ]
    evaluated with the Consumer Emergency Care Satisfaction Scale (CECSS)

  • Parental satisfaction with the health information given in the acute ward. [ Time Frame: 1-2 weeks after discharge from the hospital. An average stay in the acute ward is about 5 hours, and an average stay in the children's department is 2 days. ] [ Designated as safety issue: No ]
    Evaluated with a structured telephone interview 1-2 weeks after hospital discharge, performed by the main researcher.


Enrollment: 101
Study Start Date: January 2011
Study Completion Date: August 2011
Primary Completion Date: March 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: multimedia information
Health information concerning the child's diagnosis, treatment and recovery time after evaluation by the pediatrician, using a 15 minutes long standardized health information package with multimedia elements from the Norwegian website www.syktbarn.no (English version: www.childhealthguide.com)
Behavioral: Multimedia information
Active Comparator: verbal information
Verbal health information by a nurse in the acute ward concerning the child's diagnosis, treatment and recovery time, after the evaluation by the pediatrician
Behavioral: verbal information

Detailed Description:

The intervention website www.syktbarn.no is an open Norwegian online resource for parents of small children, and the site contains videos, audio clips, animations, illustrations, pictures and text materials regarding children's illnesses and normal development. In addition, the parents can use an interactive symptom checker that will help them to decide what to do and when to seek medical advice when their child is sick. The uniqueness of the website is the authentic video clips of sick children with common childhood symptoms like breathing difficulties, signs of dehydration, rash, cough and fever.

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • parents of 0-15 years old children with breathing difficulties caused by LRTI (bronchiolitis, laryngitis or pneumonia) or asthma exacerbation
  • ability to communicate and read Norwegian

Exclusion Criteria:

  • parents of children with chronic diseases who have direct access to the acute ward, children with oxygen saturation less than 90 %, or other very sick children who need urgent treatment
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01659879

Locations
Norway
Department of Pediatrics, St. Olav's University Hospital
Trondheim, Norway
Sponsors and Collaborators
Norwegian University of Science and Technology
St. Olavs Hospital
Investigators
Study Director: Jon Skranes, MD, PhD Norwegian University of Science and Technology
Principal Investigator: Henrik Døllner, MD, PhD St. Olavs Hospital
  More Information

Additional Information:
No publications provided by Norwegian University of Science and Technology

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Norwegian University of Science and Technology
ClinicalTrials.gov Identifier: NCT01659879     History of Changes
Other Study ID Numbers: LBK-2010/12-1
Study First Received: August 2, 2012
Last Updated: August 3, 2012
Health Authority: Norway: Norwegian Social Science Data Services

Keywords provided by Norwegian University of Science and Technology:
Parents
Caregivers
Anxiety
Consumer satisfaction

ClinicalTrials.gov processed this record on October 23, 2014