NCT01938053

Brief Summary

The primary goal of this project is to improve the process for contacting patients that test positive for a sexually transmitted infection (STI) in the emergency department by using text messaging. We believe patients that are contacted by both a phone call and a text message will be reached more often and they will be reached sooner than those that only receive a phone call or only a text message. In addition, patients will be given reminder cards at the time of testing to remind them that they will be contacted within 7 days if they test positive. Half of the reminder cards will have a number to call for test results. We believe patients that receive a card with a number are more likely to be contacted within 7 days.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
609

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Apr 2011

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2011

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2013

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

September 5, 2013

Completed
5 days until next milestone

First Posted

Study publicly available on registry

September 10, 2013

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2013

Completed
Last Updated

September 16, 2020

Status Verified

September 1, 2020

Enrollment Period

2.2 years

First QC Date

September 5, 2013

Last Update Submit

September 14, 2020

Conditions

Keywords

STI, STD

Outcome Measures

Primary Outcomes (1)

  • Contact rate

    The percentage of patients that are contacted within 7 days of their emergency department visit

    7 days

Study Arms (2)

Reminder card with no number

OTHER

Patients receive a card to remind them of the time frame for results but no number is listed.

Other: Call when test results are readyOther: Text message when test results are readyOther: Call and text message when test results are ready

Card with number

OTHER

Patients receive a card to remind them of the time frame for results but and a number to call for results is listed

Other: Call when test results are readyOther: Text message when test results are readyOther: Call and text message when test results are ready

Interventions

Patients are called when the test results are ready

Card with numberReminder card with no number

Patients receive a text message when results are ready

Card with numberReminder card with no number

Patients receive both a call and a text message when test results are resay

Card with numberReminder card with no number

Eligibility Criteria

Age14 Years - 21 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • to 21 years old
  • Seen in the emergency department at Cincinnati Children's Hospital Medical Center
  • Test positive for an STI

You may not qualify if:

  • Seen for a psychiatric evaluation
  • Seen for sexual assault or abuse

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio, 45229, United States

Location

MeSH Terms

Conditions

Sexually Transmitted Diseases

Interventions

CD56 Antigen

Condition Hierarchy (Ancestors)

Communicable DiseasesInfectionsGenital DiseasesUrogenital DiseasesDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Neural Cell Adhesion MoleculesCell Adhesion Molecules, NeuronalCell Adhesion MoleculesMembrane GlycoproteinsGlycoproteinsGlycoconjugatesCarbohydratesProteinsAmino Acids, Peptides, and ProteinsMembrane ProteinsAntigens, Differentiation, T-LymphocyteAntigens, DifferentiationAntigens, SurfaceAntigensBiological FactorsBiomarkers

Study Officials

  • Jennifer Reed, MD

    Children's Hospital Medical Center, Cincinnati

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
FACTORIAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 5, 2013

First Posted

September 10, 2013

Study Start

April 1, 2011

Primary Completion

June 1, 2013

Study Completion

December 1, 2013

Last Updated

September 16, 2020

Record last verified: 2020-09

Locations