A Trial Assessing the Effectiveness of Text Messages in Improving Continuation of Birth Control

NCT ID: NCT01545609

Last Updated: 2013-12-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

220 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-03-31

Study Completion Date

2013-11-30

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Initiation of a Birth Control Method

Keywords

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Text messaging birth control adolescents

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Text messaging

Text messaging

Group Type EXPERIMENTAL

Text messaging

Intervention Type OTHER

Text messages to cell phone with education messages about the specific birth control they are using

No intervention

No intervention

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Text messaging

Text messages to cell phone with education messages about the specific birth control they are using

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* female
* Aged 15-19 years old
* English speaking
* owner of a working cell phone
* patient must be wanting to start a birth control method and not have been on a method for preceding 3 months
* no contra indications to initiating a birth control method

Exclusion Criteria

* male
* younger than 15 years old, older than 19 years old
* already on a birth control method
* Not English speaking
* No working cell phone in possession
Minimum Eligible Age

15 Years

Maximum Eligible Age

19 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Icahn School of Medicine at Mount Sinai

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jenny Francis, MD

Role: PRINCIPAL_INVESTIGATOR

Mount Sinai Adolescent Health Center

Locations

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Mount Sinai Adolescent Health Center

New York, New York, United States

Site Status

Countries

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United States

References

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Other Identifiers

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HS#: 11-01558

Identifier Type: -

Identifier Source: secondary_id

GCO 11-1385

Identifier Type: -

Identifier Source: org_study_id