Cluster, Randomized Trial on Long Acting Reversible Contraception (LARC) Education and Training

University of California San Francisco (UCSF)

Status: Completed

Conditions: Contraception Behavior

Treatments: Behavioral: LARC education and training

Study type: Interventional

Funder types: Other

Identifiers

NCT01360216

2010-5442

Details and patient eligibility

About

The purpose of the study is to measure whether an education and training intervention for clinicians and contraceptive counselors on long-acting reversible contraception (LARC) will result in greater use of the methods among contraceptive patients.

Full description

Unintended pregnancy is extremely high in the United States among young women, and use of contraceptives with top-tier effectiveness, intrauterine contraception and implants, is low. Contraceptive providers in the US have low knowledge of current scientific evidence on LARC methods, and do not routinely include these methods in counseling patients at highest risk of unintended pregnancy. This intervention provides evidence-based education and hands-on training to clinicians and contraceptive educators in Planned Parenthood affiliated Title X clinics throughout the US on LARC methods.

Enrollment: 1,500 patients

Sex: Female

Ages: 18 to 25 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

This study involves two groups of human subjects: patients and staff at participating Planned Parenthood (PP) clinics in the United States.

Patient participants are young women receiving contraceptive counseling at Planned Parenthood clinics and staff participants are the clinicians and health educators serving these women.

Patients must be:

Female;

• Age 18-25;
• Fluent in English or Spanish;
• Not wanting to become pregnant in the next 12 months;
• Sexually active in past 3 months;
• At risk of pregnancy;
• Received contraceptive counseling;
• Not pregnant;
• Willing to be contacted by telephone over the next 12 months.

Clinic staff must be:

• Employed by a participating PP clinic; and
• Offer clinical care, counseling or education for abortion or contraception at the clinic. (This may include physicians, advance practice clinicians, nurses, social workers and health educators.)

For clinics to be eligible to be study sites, they must:

• Not share staff
• Have no active LARC interventions ongoing
• Have >400 clients/year

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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1,500 participants in 2 patient groups

LARC education and training

Experimental group

Description:

Clinicians and contraceptive educators practicing in clinics assigned to this arm receive a special half-day Continuing Medical Education (CME/CEU) accredited LARC education and training session.

Treatment:

Behavioral: LARC education and training

Standard practice- control

No Intervention group

Description:

Clinicians and contraceptive educators practicing in clinics assigned to this arm do not receive special LARC training and education session. Standard practice will be followed at clinics assigned to the control arm.