Adolescent to Adult-Oriented Health Care Transition Survey: Study of a Video-Based Educational Intervention
1 other identifier
interventional
152
1 country
1
Brief Summary
Purpose: To understand the baseline knowledge on the transition of care to adult providers in hospitalized adolescent patients and to test if an educational intervention given during an inpatient stay in a medium size academic pediatric hospital affects perception of knowledge, attitudes and participation in transition planning. Primary Research Question: Will a video-based educational intervention in an academic pediatric hospital affect perception of knowledge, attitudes and participation in transition planning to adult oriented health care of the hospitalized adolescent? Secondary Research Question: What is the baseline experience of the hospitalized adolescent in key elements of transitioning to adult oriented health care?
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Nov 2013
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2013
CompletedFirst Submitted
Initial submission to the registry
May 1, 2015
CompletedFirst Posted
Study publicly available on registry
June 24, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2015
CompletedFebruary 22, 2016
June 1, 2015
2.1 years
May 1, 2015
February 19, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Measure the number of subjects who showed a positive change in perception of transition knowledge in survey responses pre and post intervention
Will measure primary outcomes using likert scales ( eg very interested, somewhat interested, not very interested and not interested) Will compare pre and post intervention in intervention group and will compare intervention group to control group pre and post intervention.
2 years
Measure the number of subjects who showed a positive change in attitudes about transition in survey responses pre and post intervention.
Will measure primary outcomes using likert scales ( eg very interested, somewhat interested, not very interested and not interested) Will compare pre and post intervention in intervention group and will compare intervention group to control group pre and post intervention.
2 years
Measure the number of subjects who showed a positive change in participation in transition planning in survey responses pre and post intervention
Will measure primary outcomes using likert scales ( eg very interested, somewhat interested, not very interested and not interested) Will compare pre and post intervention in intervention group and will compare intervention group to control group pre and post intervention.
2 years
Secondary Outcomes (1)
Measure the number of subjects who had a positive baseline survey response in hospital experience
2 years
Study Arms (2)
Video Intervention Group
EXPERIMENTALSubjects will be randomized to intervention group where participants will be asked to watch a 7 minute educational video.
Control Group
NO INTERVENTIONSubjects will be randomized to control group ( no intervention) and receive standard of educational care on adolescent to adult oriented health care transitions.
Interventions
The video highlights key elements found in the existing literature critical for transition including understanding and taking charge of their health, creating a medical summary, learning more about health insurance, introducing the idea of organizing a health care transition team and creating a plan. The video also educates patients on the opportunities to take a tour of an adult floor, talk with social workers and learn more about adult providers during their hospital stay.
Eligibility Criteria
You may not qualify if:
- Critically ill, as defined as being ICU patients;
- Patients with acute psychosis;
- Patients boarding within the pediatric hospital admitted to an adult hospital service;
- Patients who have previously viewed the video;
- Intellectually disabled;
- Non -English speaking subjects and patients who have previously participated in the study.
- For patients with an intellectual disability investigators will defer to the parents' judgment whether the patient can complete the surveys independently.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Rochesterlead
- Academic Pediatric Associationcollaborator
Study Sites (1)
Golisano Children's Hospital at Strong
Rochester, New York, 14642, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Keely E Dwyer-Matzky, MD
University of Rochester
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
May 1, 2015
First Posted
June 24, 2015
Study Start
November 1, 2013
Primary Completion
December 1, 2015
Study Completion
December 1, 2015
Last Updated
February 22, 2016
Record last verified: 2015-06