Northwestern Memorial Hospital
Chicago, Illinois, 60611, United States
Location status: Recruiting
NCT Number: NCT06941974
The Partnering with Antenatal Navigators to Transform Health in Pregnancy (PATH) study aims to evaluate whether an antenatal patient navigation program improves maternal health, neonatal health, pregnant women's experiences, and health care utilization outcomes among low-income pregnant women and their neonates. Patient navigation is an individualized, barrier-focused, longitudinal, patient-centered intervention that offers support for a defined set of health services. In this randomized controlled trial, pregnant women who are randomized to receive antenatal patient navigation will be compared to pregnant women who are randomized to receive usual care. Navigators will support pregnant women from before 20 weeks of gestation through 2 weeks postpartum. The PATH intervention will be grounded in understanding and addressing factors that influence health and access to care in order to promote self-efficacy, enhance access, and sustain long-term engagement.
The main objectives of the study are to:
1. Evaluate whether PATH, compared to usual care, improves maternal health outcomes. We hypothesize the PATH model of antenatal patient navigation for low-income women will reduce the incidence of a composite of adverse maternal outcomes, all of which are known to be increased among women with barriers to care. 2. Evaluate whether PATH, compared to usual care, improves perinatal health outcomes. We hypothesize PATH will reduce the incidence of a composite of adverse perinatal outcomes. We will also investigate neonatal/pediatric health care utilization. 3. Evaluate patient, clinician, navigator, and healthcare system experiences with PATH in preparation for widespread implementation and dissemination of the PATH obstetric navigation model. This aim will be accomplished through investigating patient-reported outcomes, completing qualitative and process mapping interviews with navigated participants, and completing qualitative and process mapping interviews with clinicians, navigators, and health administrators.
Interested in participating?
Request Info16 year–50 year
Female
Interventional
Not applicable
Chicago, Illinois, 60611, United States
Location status: Recruiting
In the US, high rates of maternal morbidity are urgent public health concerns. Limited access to health care combined with other non-medical challenges generate greater risk of adverse maternal and neonatal outcomes for women with low income. High-quality antenatal care supports optimal health, yet typically fails to meet the needs of some populations, including those with lower incomes. Improving the health of pregnant women in a patient-centered manner requires innovative models of care delivery across the spectrum of maternal care. One strategy is patient navigation, a longitudinal, barrier- focused, patient-centered intervention that offers support for health services. Our prior work has included the study of patient navigation for low-income postpartum women, finding that assignment to a navigator improves the receipt of postpartum care and the successful transition to primary care. Although antenatal care is an ideal setting for patient navigation, the benefits of antenatal patient navigation for overall maternal and perinatal health have not been rigorously evaluated in randomized trials. There has been no study of antenatal patient navigation as a comprehensive, wraparound service to improve a wide range of pregnancy outcomes.
This randomized controlled trial aims to test the efficacy of an innovative antenatal care patient navigation model that extends and expands care for low-income pregnant women via the Partnering with Antenatal Navigators to Transform Health in Pregnancy (PATH) Trial. We will randomize nulliparous pregnant women with low income to receive antenatal patient navigation via the PATH program versus usual antenatal care. Participants randomized to receive PATH navigation will receive intensive, individualized patient navigation services throughout pregnancy. As a multilevel, multidomain, intervention, PATH navigation is grounded in understanding and addressing approaches to promote self-efficacy, enhance access, support communication, and sustain healthcare engagement. The PATH navigation program is a comprehensive antenatal patient navigator program which is guided by principles of barrier ascertainment and reduction, promotion of self-efficacy and health literacy skills, facilitation of communication, and enhancing antenatal care access. PATH navigators will incorporate best practices regarding non-medical needs assessment, motivational interviewing, health education, and capacity-building health behavior support.
The study will enroll and randomize 550 to 600 pregnant women, ages 16 and over, who have not had a previous live birth and who have publicly funded prenatal care or have low income. Participants assigned to navigation will be provided intensive, individualized, one-on-one navigation services from enrollment (at less than 20 weeks of gestation) through 2 weeks postpartum. All participants will undergo surveys, interviews, and medical record reviews at 5 study visits from enrollment (<20 weeks of gestation) through 9 months postpartum. Visits will occur at the following intervals: before 20 weeks (V1), 28-32 weeks of gestation (V2), at the time of hospitalization for delivery (V3), 6-12 weeks postpartum (V4), and 9 months postpartum (V5).
Aim 1 will evaluate whether PATH, compared to usual care, improves a composite of maternal adverse outcomes (including hypertensive disorders, preterm birth, postpartum hemorrhage, severe maternal morbidity, maternal mortality). Sub-Aim 1 aims to evaluate whether PATH, compared to usual care, improves effective maternal healthcare utilization (antenatal hospital use, Adequacy of Prenatal Care Utilization index, postpartum care/admission). Aim 2 will evaluate whether PATH, compared to usual care, improves a composite of perinatal adverse outcomes (including neonatal intensive care unit admission, low birthweight, small- and large-for-gestational age, perinatal death). Sub-Aim 2 aims to evaluate whether PATH, compared to usual care, improves effective neonatal/pediatric healthcare utilization (neonatal length-of-stay, neonatal hospital utilization, and pediatric care attendance). Exploratory Aims 1 and 2 will evaluate whether PATH's efficacy varies by different demographic factors (e.g. age), or chronic disease status.
Aim 3 will evaluate patient, clinician, navigator, and health system experiences with PATH in preparation for widespread implementation and dissemination of the PATH obstetric navigation model. This aim is guided by implementation science principles and will be accomplished via serial collection of patient-reported outcomes, individual interviews, and process mapping exercises. Specifically, Aim 3a will compare patient-reported outcomes, including perceived health status, quality of life, patient activation, stress level, and self-efficacy, for women who receive PATH navigation versus usual care. Aim 3b will use qualitative and process mapping methods among approximately 50 participants assigned to PATH to understand participants' engagement, feedback, pregnancy experience, antenatal care processes, and satisfaction with the level of social and medical care received with patient navigation. Aim 3c will similarly use qualitative and process mapping methods with approximately 20 clinicians, navigators, and health system administrators to understand the extent to which PATH facilitated clinical, administrative, and health system needs, as well as lessons for future program implementation, including the relative benefits of discrete elements of the PATH intervention.
The PATH Trial will fill a significant evidence gap by demonstrating whether antenatal patient navigation among low-income pregnant women, who are disproportionately at risk for adverse outcomes, is an effective strategy to improve perinatal health. The expected outcome of this project is to generate the empiric evidence needed to understand the effect of antenatal patient navigation and to plan for an optimized package of successful implementation strategies to prepare for broad dissemination.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion:
PATH navigation is an antenatal patient navigator program designed to reduce barriers to care, enhance access, improve self-efficacy and knowledge, and improve multiple perinatal health outcomes. PATH navigation is a flexible, multi-pronged, patient-centered program with the capacity to evolve with patient needs and preferences. Early in pregnancy, navigators will establish themselves as a non-medical resource and will introduce PATH as a program designed to help inform, support, and connect patients during pregnancy. Navigators will review screen and address supportive and adverse non-medical needs, facilitate communication, perform logistical support, provide advocacy and bridge communication with clinical teams, and perform health education. Navigation services will be tailored to individual medical, psychosocial, or logistical complexity.
Time frame: Enrollment through delivery hospitalization, an average of 28 weeks
Frequency of maternal composite, which includes hypertensive disorders of pregnancy, preterm birth, postpartum hemorrhage, severe maternal morbidity, or maternal mortality. Components of the primary outcome will also be examined as a score and individually as secondary outcomes (see below).
Time frame: At birth/delivery
Frequency of the neonatal composite, which includes neonatal intensive care unit (NICU) admission, low birthweight, small-for-gestational-age (SGA), large-for-gestational-age (LGA) status, and/or perinatal death. Components of the composite outcome will also be examined as a score and individually as secondary outcomes (see below).
Time frame: Enrollment through delivery hospitalization, an average of 28 weeks
Frequency of de novo hypertensive disorder of pregnancy, including gestational hypertension, preeclampsia with or without severe features, superimposed preeclampsia on chronic hypertension, eclampsia, or HELLP syndrome
Time frame: Enrollment through delivery hospitalization, an average of 28 weeks
Frequency of birth less than 37 weeks of gestation
Time frame: At birth/delivery
Frequency of estimated/quantitative blood loss >1000mL (during delivery hospitalization) or blood transfusion
Time frame: Enrollment through delivery hospitalization, an average of 28 weeks
Frequency of CDC-defined indicators for severe maternal
Time frame: Enrollment through delivery hospitalization, an average of 28 weeks
Frequency of maternal death (any reason) during pregnancy or the delivery hospitalization
Time frame: At birth/delivery
Frequency of admission to the neonatal intensive care unit
Time frame: Immediately post-birth
Frequency of birth weight <2500g
Time frame: Immediately post-birth
Frequency of birth weight <10%ile for gestational age and sex
Time frame: Immediately post-birth
Frequency of birth weight >90%ile for gestational age and sex
Time frame: 20 weeks of gestational through birth hospitalization
Frequency of intrauterine fetal demise (>20 weeks of gestation) or neonatal death (i.e., antenatal, intrapartum, or neonatal death)
Time frame: Enrollment through delivery
Frequency of unanticipated obstetric triage or emergency department visit, or antepartum admission
Time frame: Enrollment through delivery
Adequacy of Prenatal Care Utilization Index score
Time frame: Between delivery and 12 weeks after delivery
Frequency of attendance at a routine postpartum care visit within 12 weeks after delivery
Time frame: Between delivery and 9 months postpartum
Frequency of hospital readmission or emergency department use within 9 months of delivery
Time frame: During birth hospitalization
Neonatal length of birth hospitalization (days)
Time frame: From birth hospital discharge through 9 months
Frequency of neonatal emergency department visit or hospital admission
Time frame: From birth hospital discharge through 9 months
Frequency of attendance at indicated neonatal/pediatric outpatient care in the recommended time frame in the first 9 months of life
Time frame: During pregnancy, delivery hospitalization, 6-12 weeks postpartum, and 9 months postpartum
PROMIS Global Health score
Time frame: During pregnancy, delivery hospitalization, 6-12 weeks postpartum, and 9 months postpartum
Short Form Health Survey score
Time frame: During pregnancy, delivery hospitalization, 6-12 weeks postpartum, and 9 months postpartum
Patient Health Questionnaire-9 score
Time frame: During pregnancy, delivery hospitalization, 6-12 weeks postpartum, and 9 months postpartum
General Anxiety Disorder-7 score
Time frame: During pregnancy, delivery hospitalization, 6-12 weeks postpartum, and 9 months postpartum
PROMIS Self-Efficacy-General score
Time frame: During pregnancy, delivery hospitalization, 6-12 weeks postpartum, and 9 months postpartum
Consumer Health Activation Index score
Time frame: During pregnancy, delivery hospitalization, and 6-12 weeks postpartum
nuMoM2b Difficulties in Pregnancy Scale score
Time frame: 3rd trimester, delivery hospitalization
nuMoM2b Pregnancy Experience Scale-Brief score
Time frame: During pregnancy, delivery hospitalization, 6-12 weeks postpartum, and 9 months postpartum
Perceived Stress Scale score
Time frame: During pregnancy, delivery hospitalization, and 6-12 weeks postpartum
Prenatal Care Satisfaction Scale score and modified scale for postpartum care satisfaction
Time frame: Enrollment through delivery hospitalization, an average of 28 weeks
Participants randomized to receive navigation will complete in-depth qualitative interviews on their experiences with the navigation program. Interviews will address satisfaction with social and medical care received, engagement with the program, antenatal care experience, relationship with the navigator, experience with PATH navigation, and areas for improvement. Interviews will also include process mapping to understand antenatal care processes and PATH's contributions to their optimization
Time frame: During pregnancy and through 9 months postpartum
Survey - Patient Satisfaction with Interpersonal Relationship with Navigator Scale (among participants receiving navigation)
Time frame: During pregnancy and through 9 months postpartum
Survey - Patient Satisfaction with Logistical Aspects with Navigator Scale (among participants receiving navigation)
Time frame: Through completion of study, an average of 5 years
Clinicians, navigators, and administrators will complete in-depth interviews and process mapping exercises. Interviews will solicit their input whether PATH is successful, preferred patient navigation elements, and how they perceive PATH to affect patient care. Interviews will also include implementation science-guided process mapping exercises to understand how PATH navigation intersects with system-level healthcare, patient-level needs, and organizational processes.
Time frame: Through completion of study, an average of 5 years
Mixed methods data on navigation intensity (number of interactions over the duration of intervention performance), types of activities completed for/with participants, types of communication modes used, and types of health care team interactions. Data will be integrated from navigator logs of navigation activities and quarterly in-depth qualitative interviews with the navigators.
Contact information is provided by the study sponsor or research team.
Brittney R Williams, MPH
CONTACT
Lynn M Yee, MD, MPH
CONTACT
Northwestern University
Other
Acronym: PATH
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07274527
Amnioinfusion, CPAP
Milwaukee, Wisconsin, United States
View Trial DetailsNCT05430815
Death, Maternal Death
Atlanta, Georgia, United States
View Trial DetailsNCT02148952
Death, Female Urogenital Diseases and Pregnancy Complications
Lucknow, Uttar Pradesh, India
View Trial DetailsNCT03299491
Behavior, Communication
View Trial Details