NCT00677703

Brief Summary

Teen girls and young women taking birth control pills may forget to take their pills or may stop taking them altogether. This places them at risk for unintended pregnancies. Most young women own cell phones and use them for text messaging. We will test whether contraceptive continuation is affected after six months of daily text message reminders.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
968

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jan 2008

Longer than P75 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

January 1, 2008

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

May 12, 2008

Completed
2 days until next milestone

First Posted

Study publicly available on registry

May 14, 2008

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2010

Completed
2.3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2012

Completed
Last Updated

November 19, 2012

Status Verified

November 1, 2012

Enrollment Period

2.2 years

First QC Date

May 12, 2008

Last Update Submit

November 16, 2012

Conditions

Keywords

birth control pillscontraceptioncontinuationtext messagingcontraceptive continuationcontraceptive knowledge

Outcome Measures

Primary Outcomes (1)

  • contraceptive continuation

    6 months

Secondary Outcomes (1)

  • change in contraceptive knowledge scores

    6 months

Study Arms (2)

Standard Care

NO INTERVENTION

Participants will receive standard care without daily reminders.

Text Messages

EXPERIMENTAL

Participants will receive a daily text message reminder for 6 months

Other: Daily Text Messages

Interventions

Text message reminders to take oral contraception daily: Each text message will be a short educational message listing the benefits of contraceptive use and providing instructions for avoiding common medication errors.

Also known as: Text Messaging
Text Messages

Eligibility Criteria

AgeUp to 24 Years
Sexfemale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • aged \<25 years requesting OC as their primary method of contraception
  • currently sexually active or anticipating sexual activity within the next 30 days
  • owns cell phone with text messaging capability

You may not qualify if:

  • contraindications to combined hormonal contraception per clinic protocol (e.g., hypertension)
  • previous participation in this study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Planned Parenthood Boro Hall

Brooklyn, New York, 11201, United States

Location

Related Publications (4)

  • Castano PM, Martinez RA. Harnessing technology for adolescent health promotion. Adolesc Med State Art Rev. 2007 Aug;18(2):400-6, xiii.

    PMID: 18605654BACKGROUND
  • Castano PM, Westhoff C, Andres Martinez R, Lara M. The effect of daily text message reminders on adolescent oral contraceptive pill continuation. Journal of Adolescent Health 44(2): S17, 2009.

    RESULT
  • Hall KS, Westhoff CL, Castano PM. The impact of an educational text message intervention on young urban women's knowledge of oral contraception. Contraception. 2013 Apr;87(4):449-54. doi: 10.1016/j.contraception.2012.09.004. Epub 2012 Oct 10.

  • Castano PM, Bynum JY, Andres R, Lara M, Westhoff C. Effect of daily text messages on oral contraceptive continuation: a randomized controlled trial. Obstet Gynecol. 2012 Jan;119(1):14-20. doi: 10.1097/AOG.0b013e31823d4167.

Study Officials

  • Paula M Castano, MD, MPH

    Columbia University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Clinical Professor

Study Record Dates

First Submitted

May 12, 2008

First Posted

May 14, 2008

Study Start

January 1, 2008

Primary Completion

April 1, 2010

Study Completion

July 1, 2012

Last Updated

November 19, 2012

Record last verified: 2012-11

Locations