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| Name | Class |
|---|---|
| Academic Pediatric Association | INDUSTRY |
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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?
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.
Aim 1: To determine the effect of viewing 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.
Aim 2: To describe the baseline experience and knowledge base of hospitalized adolescents regarding key elements of transitioning to adult-oriented health care.
CHARACTERISTICS OF THE RESEARCH POPULATION
Methods and Procedures:
The purpose of the study will be achieved by surveying all eligible subjects admitted to the children's hospital. Eligible patients will be identified by the daily unit census in the children's hospital, excluding the patients outlined under exclusion criteria. Informed consent will be obtained from their parents and patients will assent to participate in the study. Personal health information and contact information will be collected with parents present by study investigator prior to randomization of subjects and will be stored separately from other survey data stored in a secure database on a password protected computer. All paper files will be kept in a locked office.
A retrospective chart review will be performed to record each subject's type of health insurance and chronic illness based on the medical chart from the current hospitalization. Comparison will be made between the patient's awareness of his underlying chronic illness and compared with health care providers' documentation of underlying chronic illness.
Data Analysis and Monitoring Data will be statistically analyzed using descriptive statistics such as mean and standard deviation, chi square testing and regression analysis. Excel, SPSS and SAS will be used for statistical calculations. Dr. Keely Dwyer-Matzky , the principal investigator will be responsible for ensuring the privacy of the data. Since there is minimal risk a data and safety monitoring plan is not necessary.
Data Storage and Confidentiality
SurveyMonkey© is a confidential proprietary survey tool that collates quantitative data and written comments into convenient reports. SurveyMonkey© uses Secure Sockets Layer (SSL) technology, which protects user information through both server authentication and data encryption, ensuring that user data is safe, secure, and available only to authorized persons. Investigators will protect all health identifiers. Data downloaded from SurveyMonkey© will be maintained on electronic files on a secure server with password protection. Only authorized researchers will have access to the data. University of Rochester Office of Human Subjects or research regulatory groups may review these records.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Video Intervention Group | Experimental | Subjects will be randomized to intervention group where participants will be asked to watch a 7 minute educational video. |
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| Control Group | No Intervention | Subjects will be randomized to control group ( no intervention) and receive standard of educational care on adolescent to adult oriented health care transitions. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Educational Video | Behavioral | 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. |
| Measure | Description | Time Frame |
|---|---|---|
| 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 |
| Measure | Description | Time Frame |
|---|---|---|
| Measure the number of subjects who had a positive baseline survey response in hospital experience | Will measure secondary outcome measures using likert scales ( eg very interested, somewhat interested, not very interested and not interested) Will compare all respondents based on age, race, gender, special health care need, health insurance and education level. | 2 years |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Keely E Dwyer-Matzky, MD | University of Rochester | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Golisano Children's Hospital at Strong | Rochester | New York | 14642 | United States |
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