Skip to content

Impact of Mobile Text Messaging on Follow Up Rates After Discharge From the Pediatric Emergency Department

Impact of Mobile Text Messaging on Follow Up Rates After Discharge From the Pediatric Emergency Department

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03674879
Enrollment
0
Registered
2018-09-18
Start date
2016-09-30
Completion date
2017-12-31
Last updated
2018-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Duty to Recontact

Keywords

Follow Up, Text Messaging

Brief summary

To compare the effectiveness of text message versus voice call as a method of contact for providing results of diagnostic tests and assuring ongoing care from the pediatric emergency department.

Detailed description

The investigators plan to conduct a prospective randomized controlled trial to compare two means of contacting patients and their caregivers after discharge from the emergency department in order to provide results of tests: text messaging (intervention group) vs. telephone call (standard group).

Interventions

OTHERText Message

Patient contact attempted with text message.

Sponsors

New York City Health and Hospitals Corporation
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* patients under the age of 18 who have had diagnostic testing without finalized results prior to discharge from the emergency department

Exclusion criteria

* Admitted patients * Patients transferred to another facility * Patients with critical values as results * Do not have devices that can receive phone and text messages * Cannot read English or Spanish

Design outcomes

Primary

MeasureTime frameDescription
Number of phone call or text message attempts to successful contact with study participantWithin 2 weeks.A study practitioner will make one attempt per business day to contact the patient or caregiver to provide test results and arrange follow-up care; the method will be determined by the study arm to which the participant is assigned. Participants in the standard practice control arm will receive a telephone call. If a call is not answered, a voice message will be left instructing the patient/parent to call the Pediatric Follow-Up Office. Participants in the intervention arm will receive a text message using the same script. A successful contact will be recorded when a practitioner speaks directly to the patient or parent/guardian via phone.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026