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A Pilot Study Using Text Messaging to Communicate With Adolescent Females in the Pediatric Emergency Department

Texting 2 Initiate: A Pilot Study Using Text Messaging to Communicate With Adolescent Females in the Pediatric Emergency Department (T2I)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02093884
Acronym
T2I
Enrollment
100
Registered
2014-03-21
Start date
2014-01-31
Completion date
2015-03-31
Last updated
2017-01-20

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

Conditions

Pregnancy

Keywords

Pregnancy, Pregnancy, unplanned, Reproductive behavior, Pregnancy in Adolescence, Text messaging

Brief summary

The objective of this study is to develop and test an emergency department (ED)-based intervention which uses text messages to facilitate contraception initiation.

Detailed description

Our hypothesis is that adolescent females at high pregnancy risk who receive text message reminders and motivational messages that promote contraception and referral to the Family Planning Clinic are more likely to start effective contraception than those who receive standard paper-based referral to the Family Planning Clinic alone.

Interventions

Sponsors

Society of Family Planning
CollaboratorOTHER
Columbia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
14 Years to 19 Years
Healthy volunteers
No

Inclusion criteria

* Aged 14-19 years * Sexually active with males in the past three months * Presenting to the ED for a reproductive health complaint.

Exclusion criteria

* Presently pregnant * Too ill for participation per the attending physician * Cognitively impaired * In foster care or a ward of the state * Does not speak English or Spanish * Does not own a cellular or mobile phone with text messaging capabilities * Used contraception at last intercourse and/or is currently using any highly effective or effective form of contraception (as defined by the World Health Organization) * Does not live in Manhattan or the Bronx

Design outcomes

Primary

MeasureTime frameDescription
Initiation of highly effective contraception, as defined by the World Health Organization.3 months after initial enrollmentWe will be assessing contraception initiation rates based on electronic medical record review and telephone call follow up.

Secondary

MeasureTime frameDescription
Patient visits to Family Planning Clinic3 months after initial enrollmentWe assess Family Planning Clinic visits using our electronic medical records.
Follow up for contraceptive counseling to a doctor or nurse3 months after initial enrollmentWe will be asking patients during our phone call follow if they have had contraceptive counseling with any healthcare professional. We will also be looking through electronic medical records for documentation of contraceptive counseling such as by ICD-9 coding or a physician's/nurse's note.
Change in pregnancy intentions3 months after initial enrollmentWe will compare pregnancy intentions elicited from the answers provided in the baseline questionnaire to those reported on the telephone follow up for both study arms.

Other

MeasureTime frameDescription
Text messaging intervention safety3 months after initial enrollmentSafety will be assessed during the telephone follow up.

Countries

United States

Outcome results

None listed

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