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Using Social Media to Decrease Healthcare Utilization for Pediatric Asthma

Primary Purpose

Asthma in Children

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Social Media Enhanced Education
Usual Asthma Education
Sponsored by
The University of Texas Health Science Center, Houston
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Asthma in Children focused on measuring Social Media, Pediatric Asthma, Healthcare Utilization

Eligibility Criteria

3 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • hospitalized to Children's Memorial Hermann admitted for asthma exacerbation
  • patient and/or primary caregiver must have internet access on cellular phones or at home and use a social media account (Facebook, Twitter, Instagram, and/or Snapchat)

Exclusion Criteria:

  • other chronic conditions besides asthma that may necessitate frequent health care utilization. i.e. children with complex chronic conditions, sickle cell, seizures, diabetes.

Sites / Locations

  • The University of Texas Health Science Center at HoustonRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Treatment

Control Group

Arm Description

Outcomes

Primary Outcome Measures

Total number of treatment days in a medical setting (hospital, emergency department (ED), clinic)
Treatment days are defined as the summation of days in the hospital, ED, or in the clinic.

Secondary Outcome Measures

Total number of hospitalizations
total number of readmissions
total number of emergency room visits
total number of clinic visits
patient satisfaction and understanding of asthma education
This is a 13 item questionnaire each question is rated from 1 to 5 a higher number indicating a better outcome
number of missed days of school
total estimated health system costs, hospital costs, and clinic costs

Full Information

First Posted
August 13, 2021
Last Updated
May 9, 2023
Sponsor
The University of Texas Health Science Center, Houston
Collaborators
National Center for Advancing Translational Sciences (NCATS)
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1. Study Identification

Unique Protocol Identification Number
NCT05013788
Brief Title
Using Social Media to Decrease Healthcare Utilization for Pediatric Asthma
Official Title
Using Social Media to Decrease Healthcare Utilization for Pediatric Asthma: a Pilot Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 1, 2021 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Texas Health Science Center, Houston
Collaborators
National Center for Advancing Translational Sciences (NCATS)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate if social media enhanced education (SME) will reduce total number of treatment days defined as summation of days of subsequent hospital admission, emergency room visits, and clinic visits, reduce missed school days, reduce total costs from a health system perspective, have increased effect with increased social media engagement, have increased effect in participants with both caregiver and patient (combined) with social media accounts, compared to participants where only the patient or only the caregiver uses social media (single),have increased patient satisfaction in the asthma education received and to obtain the experience and data needed to refine SME to be able to expand this platform for other chronic medical conditions with high healthcare utilization including pediatric diabetes, epilepsy, and sickle cell disease in children with asthma.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma in Children
Keywords
Social Media, Pediatric Asthma, Healthcare Utilization

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Treatment
Arm Type
Experimental
Arm Title
Control Group
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
Social Media Enhanced Education
Intervention Description
Along with usual asthma education received,participants will receive asthma education via various social media platforms ,Facebook, Twitter, Instagram, and/or Snapchat. Topics of education will include background on asthma and pathophysiology, asthma severity classification, asthma triggers, different medications and indications for when to take them, how to use an inhaler technique, and symptom monitoring.Online resources from the American Lung Association and the National Asthma Education and Prevention Program will also be posted.
Intervention Type
Other
Intervention Name(s)
Usual Asthma Education
Intervention Description
For patients who are admitted to Children's Memorial Hermann for asthma exacerbation, asthma education is provided to patients and families on the day of discharge by the nurse and respiratory therapist on triggers, Signs & Symptoms, Medication Use, Medication Delivery, Peak Flow, Zones and how to respond to each, and Cleaning equipment.Nursing staff are responsible for printing out education sheets to give to patients and showing an education video that is 20 minutes long. An asthma action plan are given to families on discharge. Patients that are discharged from the emergency room are given the same educational materials by the nurses and/or respiratory therapists except for the asthma video. Patients receive a variable amount of asthma education when going to usual clinic visits. The education provided is dependent on the provider, and usually limited in length to the time of the visit
Primary Outcome Measure Information:
Title
Total number of treatment days in a medical setting (hospital, emergency department (ED), clinic)
Description
Treatment days are defined as the summation of days in the hospital, ED, or in the clinic.
Time Frame
1 year after enrollment
Secondary Outcome Measure Information:
Title
Total number of hospitalizations
Time Frame
1 year after enrollment
Title
total number of readmissions
Time Frame
1 year after enrollment
Title
total number of emergency room visits
Time Frame
1 year after enrollment
Title
total number of clinic visits
Time Frame
1 year after enrollment
Title
patient satisfaction and understanding of asthma education
Description
This is a 13 item questionnaire each question is rated from 1 to 5 a higher number indicating a better outcome
Time Frame
1 year after enrollment
Title
number of missed days of school
Time Frame
1 year after enrollment
Title
total estimated health system costs, hospital costs, and clinic costs
Time Frame
1 year after enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: hospitalized to Children's Memorial Hermann admitted for asthma exacerbation patient and/or primary caregiver must have internet access on cellular phones or at home and use a social media account (Facebook, Twitter, Instagram, and/or Snapchat) Exclusion Criteria: other chronic conditions besides asthma that may necessitate frequent health care utilization. i.e. children with complex chronic conditions, sickle cell, seizures, diabetes.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Raymond Parlar-Chun, MD
Phone
(713) 500-5666
Email
Raymond.L.Chun@uth.tmc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Raymond Parlar-Chun, MD
Organizational Affiliation
The University of Texas Health Science Center, Houston
Official's Role
Principal Investigator
Facility Information:
Facility Name
The University of Texas Health Science Center at Houston
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Raymond Parlar-Chun, MD
Phone
713-500-5666
Email
Raymond.L.Chun@uth.tmc.edu

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Using Social Media to Decrease Healthcare Utilization for Pediatric Asthma

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