Among people who do not want to get pregnant, some do not use any birth control. This is also called contraceptive nonuse. Common reasons for contraceptive nonuse include concerns about birth control safety or side effects. People with health conditions, such as diabetes or high blood pressure, also report worries about how different birth control methods might affect their health condition or medicines. The goal of this clinical trial is to learn if a web tool called My Health, My Choice helps people with health conditions understand their birth control options and choose birth control that is right for them. The study will also look at the medical safety of birth control methods that participants decide to use. The main questions it aims to answer are: • Does the My Health My Choice tool lower the number of participants who do not use any birth control method? (contraceptive nonuse) In other words, does the My Health My Choice tool increase the number of participants who use any birth control method? (contraceptive use) Participants who use the My Health, My Choice tool before a clinic visit with their clinician (Intervention Group) will be compared to participants who only go to a clinic visit with their clinician (Usual Care Group). For this study, a "clinician" is any licensed health care provider who counsels about birth control, prescribes birth control, and/or inserts birth control devices. All participants will: * Complete 4-5 online surveys that take 5-10 minutes each, over a 3 month time period * Be asked to go to a scheduled clinic visit with their health care provider * A small group of participants (about 30) will be invited to a 1 hour exit interview Participants in the intervention arm will be asked to: • Use the My Health My Choice tool before their clinic visit
Fourteen outpatient clinics in the United States that provide birth control services, including primary care and obstetrics and gynecology clinics, will be enrolled. Each clinic will be randomly assigned to the My Health My Choice Group (intervention group) or the Usual Care group. Only patients who receive health care at enrolled clinics are eligible for study participation. Participants must be aged 18-49 years, read English, fertile (able to get pregnant), have at least one index health condition, characteristic or medication usage (full list of 60+ eligible conditions, characteristics, and 50+ medications available upon request); and want to talk about birth control at an upcoming clinic visit with their clinician. Eligible participants will be enrolled over the phone. Enrolled participants will complete a baseline electronic survey about their demographics, health history, contraceptive use, and contraceptive knowledge before learning which study group they are in. Study Activities for Participants in the Intervention Arm Only: * Before their scheduled clinic visit, open and use the My Health My Choice tool via a password-protected weblink on a mobile device, computer * Complete a brief electronic survey about their experience using the My Health My Choice web tool. Study Activities for All Participants: * Go to their scheduled clinic visit with their clinician * Complete a survey shortly after the clinic visit * Complete a survey 1 month after the clinic visit * Complete a survey 3 months after the clinic visit All surveys take about 5-10 minutes to complete. About 30 participants across all clinic sites will be asked to do an optional 1 hour exit interview by phone or teleconference. Clinicians who provide contraceptive care, including residents who have finished their intern year, are eligible to participate. Eligible clinicians include doctors, nurse practitioners, physician assistants, and certified nurse midwives. Enrolled clinicians will complete a brief baseline and exit survey about their contraceptive counseling, the type of contraceptive methods they provide, and their contraceptive knowledge. Activities for All Clinicians * Complete a baseline survey * Complete an exit survey * Provide care to enrolled patients at their scheduled visits * Complete a brief survey after each visit with an enrolled patient Activities for Clinicians in the Intervention Arm Only • Before or during the scheduled clinic visit, open and use Clinician Version of the My Health My Choice tool via a password-protected weblink on a mobile device, computer The Clinician Version of the My Health My Choice has information to help clinicians counsel patients with health conditions about the safety of different birth control methods. Clinicians can also review the "Birth Control Summary" of enrolled patients before or during the clinic visit. All clinician surveys take 3-10 minutes to complete. About 30 clinician participants across all clinic sites will be asked to participate in an optional 1 hour exit interview by phone or teleconference. After patients exit the study, an electronic health record (EHR) review will be done to find out if participants got birth control prescriptions or birth control devices during the study. The EHR review also includes checking if participants report plans to get permanent birth control (tubal sterilization for themselves or vasectomy for their partners). The primary and secondary outcomes are patient-reported or patient-related outcomes. There are no primary or secondary outcomes for clinicians. The study aims to enroll 725 patients and 70 clinicians (795 in total).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
795
The My Health My Choice decision tool is a web-based interactive tool designed to educate patients with health conditions about their contraceptive options, elicit their personal preferences and contraceptive concerns, and help them prepare for a contraceptive discussion with their clinician. Patients can compare features of different contraceptive methods side-by-side and grouped by medical risk according to the Center for Disease Control and Prevention U.S. Medical Eligibility Criteria (US MEC). The tool generates an individualized Birth Control Summary for each patient user that records their "contraceptive favorites" and their questions for the clinician. Clinicians can use the Clinician Version of the tool to review the patient's Birth Control Summary and their medical eligibility for different contraceptive methods per the US MEC guidelines.
Participants will attend clinic visits per routine. Clinicians proceed with usual contraceptive care. All study activities and incentives for participants in the usual contraceptive care arm are the same as for participants in the intervention arm except for those related to the intervention itself.
University of Arizona College of Medicine - Phoenix Department of Family, Community and Preventive Medicine - Research Division & Arizona Developing Experience with Practice-Based Research Network (PBRN) Studies
Phoenix, Arizona, United States
Pomona Valley Hospital Medical Center
Pomona, California, United States
Full Circle Health Family Medicine Residency of Idaho - Nampa Program
Nampa, Idaho, United States
University of Kansas Medical Center Department of Family Medicine & Community Health
Kansas City, Kansas, United States
MaineHealth Primary Care - Family Medicine - Sanford
Sanford, Maine, United States
Boston Medical Center's Department of Family Medicine
Boston, Massachusetts, United States
Department of Family Medicine Research Office
Ann Arbor, Michigan, United States
Von Voigtlander Women's Hospital Obstetrics and Gynecology Clinic University of Michigan Health Michigan Medicine
Ann Arbor, Michigan, United States
Michigan State University Health Care Family Medicine
East Lansing, Michigan, United States
WMed Health Family Medicine - Crosstown Parkway
Kalamazoo, Michigan, United States
...and 8 more locations
Proportion of participants who report contraceptive nonuse at 3 months
This is a binary outcome (yes/no) that will be assessed at baseline, 1 month, and 3 months after the clinic visit. Participants will report use or nonuse of a contraceptive method in the last month. Contraceptive methods include all non-prescription methods, prescription methods, intrauterine devices (IUDs), the implant, tubal ligation/surgery, and vasectomy of their partner. If patients report use of the cervical cap, condoms, diaphragm, spermicides, vaginal gel, or withdrawal, their outcome will be determined by whether they used the method at last intercourse in the prior month. Only patients who did not want to get pregnant in the last month will be included in the calculation of this outcome.
Time frame: Baseline, 1 month, and 3 months after the clinic visit
Medical Eligibility Risk (MER) Category among participants who report contraceptive method use
The Medical Eligibility Risk (MER) Category will be determined for participants who report contraceptive use at baseline, 1 month, and 3 months. Based upon the patient's health history and reported contraceptive method, two contraceptive experts blinded to patient assignment will assign the MER per the U.S. Medical Eligibility Criteria Guidelines. This is a categorical measure with four MER Categories: * Category 1: the method can be used without restriction because there are no theoretical or proven risks * Category 2: the method can be used because the advantages outweigh any theoretical or proven risks * Category 3: in general, the method should be avoided because the theoretical or proven risks of a contraceptive method usually outweigh any advantages of use. * Category 4: the method should not be used because the theoretical or proven risks outweigh any advantages.
Time frame: Baseline, 1 month, and 3 months
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