A Trial Assessing the Effectiveness of Text Messages in Improving Continuation of Birth Control (BC 2U)
|ClinicalTrials.gov Identifier: NCT01545609|
Recruitment Status : Completed
First Posted : March 7, 2012
Last Update Posted : December 24, 2013
This study is a randomized controlled trial assessing the effectiveness in a series of educational text messages in improving continuation of a birth control method in comparison to the 'standard counseling', when girls initiate a new method of birth control. Girls aged 15-19 year olds who are attending for a reproductive health visit and who own a working cell phone will be approached and asked if they would like to participate. Following completion of a baseline questionnaire and consultation for initiation of a new birth control method they will be randomized to receive either the intervention or standard counseling.
If randomized to the intervention they will receive 3 messages per week for the initial 3 weeks, 2 messages per week for the following 5 weeks and then one message per week thereafter. Messages will be tailored to the birth control method the participant has initiated. At 4 months all participants will be contacted via telephone and asked to complete a questionnaire regarding continuation of use.
|Condition or disease||Intervention/treatment||Phase|
|Initiation of a Birth Control Method||Other: Text messaging||Phase 1|
Hypothesis. A personalized text messaging program providing trustworthy, reliable information and support to female adolescents initiating a birth control method, will improve adherence and correct use of the method and so reduce unwanted pregnancies.
Methods. Female adolescents aged 15-19 year olds attending Mount Sinai Adolescent Health Center (MSAHC) for initiating a birth control method will be asked if they are interested in participating in the trial.
The Intervention Group. Upon initiation of a birth control method patients will be signed up to the text messaging platform. Via this program they will receive personalized messages regarding their chosen method of birth control. Participants will receive 3 messages during the initial 3 weeks, 2 messages per week in weeks 4-8 and then one message a week thereafter for a period of 12 months. They will be signed up for reminders to take/change their method (as appropriate) and have access to a Healthcare Provider to ask questions via text message that they may have regarding their method. Participants will be reminded (via text message) to attend the clinic for a birth control refill (if necessary) at 3, 6, 9 and 12 months.
The Control Group. Participants randomized in to the control group will have standard care. This is the usual counseling by the Health Care Provider or Health Educator. Patients in the intervention arm will also receive this standard care.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||220 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Text Message Support System for Effective Continuation of a Birth Control Method in Female Adolescents: 'BC 2U'|
|Study Start Date :||March 2012|
|Primary Completion Date :||November 2013|
|Study Completion Date :||November 2013|
Experimental: Text messaging
Other: Text messaging
Text messages to cell phone with education messages about the specific birth control they are using
No Intervention: No intervention
- Continuation of a birth control method [ Time Frame: at 4 months ]Birth control continuation will be assessed at 4 months by direct asking of the participant to see if participant has attended for a refill of her birth control method.
- Change in birth control method being used. [ Time Frame: at 4 months ]whether subjects continue with the initial method of birth control or discontinue a method at the 4 months.
- Pregnancy [ Time Frame: at 4 months ]
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01545609
|United States, New York|
|Mount Sinai Adolescent Health Center|
|New York, New York, United States, 10128|
|Principal Investigator:||Jenny Francis, MD||Mount Sinai Adolescent Health Center|