- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04410380
Patient Portal Use by Parents of Spanish-Speaking Children
March 13, 2023 updated by: University of North Carolina, Chapel Hill
The purpose of this study is to determine whether patient portal access is feasible and useful for Spanish-speaking parents.
Participants will be given an electronic tablet and will be taught how to access their child's medical record and other electronic health resources using the tablet.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
25
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
North Carolina
-
Chapel Hill, North Carolina, United States, 27599
- UNC Hospitals
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Be parent/legal guardians of children receiving care in UNC's Children's Clinics
- Have Spanish as preferred language of individual identifying as primary caregiver
- Have never activated MyChart (patient portal)
- Have internet service at home OR ability to easily access internet service
- Have at least one child under age 13
Exclusion Criteria:
- Medically unstable at time of recruitment
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Electronic tablet
Spanish-speaking parents receive electronic tablet and teaching about use
|
Spanish-speaking parents are provided with an electronic tablet and taught how to use it to access health information for their children.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Percent of Parents Activating Patient Portal
Time Frame: 6 months
|
To determine patient portal use.
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Parent Attitudes Toward Health Information Technology
Time Frame: Baseline, 1 month
|
Parent attitudes and perceptions will be assessed by survey at enrollment and 1 month after intervention.
Scale name: Reasons to use more health information technology.
Range 3-12.
Directionality: Higher scores indicate more favorable attitudes toward health information technology
|
Baseline, 1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 2, 2020
Primary Completion (Actual)
December 30, 2022
Study Completion (Actual)
December 30, 2022
Study Registration Dates
First Submitted
May 27, 2020
First Submitted That Met QC Criteria
May 27, 2020
First Posted (Actual)
June 1, 2020
Study Record Updates
Last Update Posted (Actual)
March 14, 2023
Last Update Submitted That Met QC Criteria
March 13, 2023
Last Verified
March 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 19-1545
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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