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Satisfaction Rates Among Parents of Children With Autism in the ED (ASD)

Primary Purpose

Autism Spectrum Disorder

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Questionnaire
Sponsored by
Seton Healthcare Family
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Autism Spectrum Disorder

Eligibility Criteria

2 Years - 18 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • aged 2 to 18 years
  • parent/caregiver is fluent and literate in either English or Spanish
  • parental report of a diagnosis of (1) autism, (2) autism spectrum disorder, (3) pervasive developmental disorder, (4) childhood disintegrative disorder, (5) sensory integration disorder

Exclusion Criteria:

  • triage level 1
  • physician provider unable to review questionnaire prior to seeing the patient

Sites / Locations

  • Dell Children's Medical Center of Central Texas

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Standard of Care

Questionnaire

Arm Description

The control arm participants will receive only a satisfaction survey once disposition is determined by the physician provider. The satisfaction survey will be collected by the research associated and kept in a protected location, along with all other study materials. All patients will receive standard of care, which at this institution is the help of Child Life Specialists, when they are available and requested by the physician. Physicians will be instructed to request Child Life Specialists with the same discretion as with all patients.

Participants who are randomized to the questionnaire arm will receive a patient-centered questionnaire at the beginning of their visit. This single page document will ask questions about their child including, but not limited to, diagnoses, suggestions for distraction, sensory issues that may affect their visit, and method to best administer medications. The research associate will ask them to fill it out to the best of their ability and will collect the questionnaire prior to a physician provider seeing the patient. At least one physician provider must review the questionnaire prior to seeing the patient. Once disposition is determined, the satisfaction survey will be distributed by the research associate along with an envelope for the parent to seal their survey within.

Outcomes

Primary Outcome Measures

Satisfaction Scores
Parental satisfaction as rated on a Likert Scale (1-5)

Secondary Outcome Measures

Length of Stay
ED Length of Stay
Admission rate
Hospital admission rate
Number of PIV attempts
The number of attempts necessary to obtain peripheral venous access in those patients who have been determine by the physician to need IV placement for their medical care.
Sedating medications needed for procedures
The number and type of sedating medications needed for any procedure determined to be necessary for the patient's medical care by the physician.

Full Information

First Posted
January 31, 2016
Last Updated
July 31, 2018
Sponsor
Seton Healthcare Family
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1. Study Identification

Unique Protocol Identification Number
NCT02675933
Brief Title
Satisfaction Rates Among Parents of Children With Autism in the ED
Acronym
ASD
Official Title
What Factors Effect Parental Satisfaction During Their Visit to a Pediatric Emergency Department Among Parents of Children With Autism?
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Terminated
Why Stopped
Seton IRB administratively closed this study on January 6, 2017
Study Start Date
February 2016 (undefined)
Primary Completion Date
January 6, 2017 (Actual)
Study Completion Date
January 6, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seton Healthcare Family

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is a randomized controlled trial utilizing a patient-centered questionnaire distributed to parents of children with autism. The study arm will receive the questionnaire and will be compared to the control arm, which will receive standard of care. The results of satisfaction surveys will be the primary endpoint of this study.
Detailed Description
This study is a randomized controlled trial utilizing a patient-centered questionnaire distributed to parents of children with autism. Potential study participants will be identified during the triage process through medical history taking, which is routine for the triage process at this institution. The triage nurse will be educated to alert a research associate if a patient with one of our qualifying diagnoses is identified. This study will include patients aged 2-18 with parental report of a diagnosis of (1) Autism, (2) Autism Spectrum Disorder, (3) Pervasive Developmental Disorder, (4) Childhood Disintegrative Disorder, or (5) Sensory Integration Disorder. All patients whose caregiver is fluent and literate in either English or Spanish will be included. Research associates will then attempt to obtain consent from the parent. If consent is obtained, the research associate will then attempt to obtain assent from patients aged > 6 years. If the research associate feels the child is unable to assent based on their developmental capabilities, the research associate will then indicate this on the assent form and sign in the space provided for the research associate. Once consent and assent, if applicable, are obtained, the research associate will then select an envelope from the top of a pre-randomized stack. The contents of the envelope will either contain a questionnaire and satisfaction survey for the intervention arm, or simply a satisfaction survey if in the control arm. If the intervention arm is selected, the research associate will then distribute the questionnaire to the parent and ask them to fill it out to the best of their ability. The research associate will then return to collect the questionnaire and one of the physician providers caring for the patient must review the questionnaire prior to seeing the patient. This hospital is a teaching institution and physician providers may include residents, fellows, and attendings. Once reviewed, the physician provider will sign at the bottom of the questionnaire and proceed with the encounter. Multiple providers, including nursing staff and clinical assistants may review the questionnaire as well, which will be kept on the paper chart. When the patient's disposition is determined, the research associate will distribute the satisfaction survey and an envelope for the survey to be sealed within once completed by the parent. The satisfaction survey, along with the questionnaire and any other study documents, will be collected and placed in the envelope. The envelopes will be stored in a badge-access protected office inside of a locked cabinet behind a password protected door. Only fellows, attendings, and a few fellowship-associated and research-associated providers have access to this office.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Autism Spectrum Disorder

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
116 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard of Care
Arm Type
No Intervention
Arm Description
The control arm participants will receive only a satisfaction survey once disposition is determined by the physician provider. The satisfaction survey will be collected by the research associated and kept in a protected location, along with all other study materials. All patients will receive standard of care, which at this institution is the help of Child Life Specialists, when they are available and requested by the physician. Physicians will be instructed to request Child Life Specialists with the same discretion as with all patients.
Arm Title
Questionnaire
Arm Type
Active Comparator
Arm Description
Participants who are randomized to the questionnaire arm will receive a patient-centered questionnaire at the beginning of their visit. This single page document will ask questions about their child including, but not limited to, diagnoses, suggestions for distraction, sensory issues that may affect their visit, and method to best administer medications. The research associate will ask them to fill it out to the best of their ability and will collect the questionnaire prior to a physician provider seeing the patient. At least one physician provider must review the questionnaire prior to seeing the patient. Once disposition is determined, the satisfaction survey will be distributed by the research associate along with an envelope for the parent to seal their survey within.
Intervention Type
Behavioral
Intervention Name(s)
Questionnaire
Intervention Description
There will be a single page document, a patient-centered questionnaire, distributed to parents of study participants who have been randomized to the intervention arm.
Primary Outcome Measure Information:
Title
Satisfaction Scores
Description
Parental satisfaction as rated on a Likert Scale (1-5)
Time Frame
through study completion, an average of 1 year
Secondary Outcome Measure Information:
Title
Length of Stay
Description
ED Length of Stay
Time Frame
through study completion, an average of 1 year
Title
Admission rate
Description
Hospital admission rate
Time Frame
through study completion, an average of 1 year
Title
Number of PIV attempts
Description
The number of attempts necessary to obtain peripheral venous access in those patients who have been determine by the physician to need IV placement for their medical care.
Time Frame
through study completion, an average of 1 year
Title
Sedating medications needed for procedures
Description
The number and type of sedating medications needed for any procedure determined to be necessary for the patient's medical care by the physician.
Time Frame
through study completion, an average of 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: aged 2 to 18 years parent/caregiver is fluent and literate in either English or Spanish parental report of a diagnosis of (1) autism, (2) autism spectrum disorder, (3) pervasive developmental disorder, (4) childhood disintegrative disorder, (5) sensory integration disorder Exclusion Criteria: triage level 1 physician provider unable to review questionnaire prior to seeing the patient
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Catherine E Yee, MD
Organizational Affiliation
Pediatric Emergency Medicine Fellow
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dell Children's Medical Center of Central Texas
City
Austin
State/Province
Texas
ZIP/Postal Code
78723
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
25057539
Citation
Institute of Medicine (US) Committee on Quality of Health Care in America. Crossing the Quality Chasm: A New Health System for the 21st Century. Washington (DC): National Academies Press (US); 2001. Available from http://www.ncbi.nlm.nih.gov/books/NBK222274/
Results Reference
background
PubMed Identifier
25701197
Citation
Jo H, Schieve LA, Rice CE, Yeargin-Allsopp M, Tian LH, Blumberg SJ, Kogan MD, Boyle CA. Age at Autism Spectrum Disorder (ASD) Diagnosis by Race, Ethnicity, and Primary Household Language Among Children with Special Health Care Needs, United States, 2009-2010. Matern Child Health J. 2015 Aug;19(8):1687-97. doi: 10.1007/s10995-015-1683-4.
Results Reference
background
PubMed Identifier
22456193
Citation
Autism and Developmental Disabilities Monitoring Network Surveillance Year 2008 Principal Investigators; Centers for Disease Control and Prevention. Prevalence of autism spectrum disorders--Autism and Developmental Disabilities Monitoring Network, 14 sites, United States, 2008. MMWR Surveill Summ. 2012 Mar 30;61(3):1-19.
Results Reference
background
Links:
URL
http://www.cdc.gov/nchs/slaits/cshcn.htm#2001CSHCN
Description
2001 National Survey of Children with Special Health Care Needs
URL
http://www.cdc.gov/nchs/slaits/cshcn.htm#2005CSHCN
Description
2005-2006 National Survey of Children with Special Health Care Needs
URL
http://www.cdc.gov/nchs/slaits/cshcn.htm#09-10
Description
2009-2010 National Survey of Children with Special Health Care Needs
Available IPD and Supporting Information:
Available IPD/Information Type
Satisfaction Survey
Available IPD/Information URL
https://drive.google.com/file/d/0B_NqlF7oW2UNVjY1VlQ3MmtjR1E/view?usp=sharing
Available IPD/Information Identifier
Satisfaction survey
Available IPD/Information Comments
Please email if there are any issues downloading from google drive at ceyee@seton.org
Available IPD/Information Type
Questionnaire
Available IPD/Information URL
https://drive.google.com/file/d/0B_NqlF7oW2UNdVFBXzhDRkxpdlU/view?usp=sharing
Available IPD/Information Identifier
Questionnaire
Available IPD/Information Comments
Please email me if there are any issues downloading from google drive at ceyee@seton.org

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Satisfaction Rates Among Parents of Children With Autism in the ED

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