Postpartum CareCAPSNCT04257552
Care After Pregnancy Study (CAPS): Engaging Women in Postpartum Care
A study testing Healthy Beyond Pregnancy and Pre-Scheduled Postpartum Visit in people with Postpartum Care, run by University of Pittsburgh at 1 site in United States.
Trial summary
The overarching hypothesis of our research agenda is that an intervention that engages economically disadvantaged women in personalized postpartum care will promote equality in maternal child health. Read more about this study
- Who is it for?
- Ages 12 to 50 years, women only
- Conditions the study is for
- Postpartum Care
- What is being tested?
- Healthy Beyond Pregnancy and Pre-Scheduled Postpartum Visit
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 128 participants
- Where
- 1 siteUnited States
- Study dates
- 3 Feb 2020to 2 Sep 2021
- Phase
- Interventional
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 12 to 50 years
- Women only
- No healthy volunteers
- Child, Adult
Who may be able to join
- Insured by a PA Medicaid insurance
- Pregnancy care in the Magee Womens Hospital Outpatient Clinic
Who cannot join
- Delivery less than 24 weeks
- Fetal or neonatal demise
- Women who had a postpartum tubal ligation
- Women less than 18 year of age
Trial locations and contacts
1 site in 1 country.
United States1 site
Magee Womens Hospital
Pittsburgh, Pennsylvania, 15213
About this study
Official title: Care After Pregnancy Study (CAPS): Randomized Controlled Trial of Patient Engagement After Pregnancy
The overarching hypothesis of our research agenda is that an intervention that engages economically disadvantaged women in personalized postpartum care will promote equality in maternal child health. As a first step to test our hypothesis the investigators propose the following aims:
Specific Aim 1: Measure the impact of Healthy Beyond Pregnancy on key components of postpartum care, including use of effective contraception at three and six months postpartum and breastfeeding duration at three and six months.
Specific Aim 2: Determine if Healthy Beyond Pregnancy improves adherence to health screening and linkage to follow-up care for women with cardio-metabolic complications of pregnancy.
Read the detailed description
There are profound economic inequalities in a wide range of important maternal and child health outcomes ranging from neonatal death to maternal morbidity and mortality. The overarching scientific premise for our proposal is that these inequalities stem in part from poor engagement in postpartum care by economically disadvantaged women. The investigators hypothesize that an innovative intervention grounded in empirically derived tenets of behavioral economics that includes the critical components of the American College of Obstetricians and Gynecologists (ACOG) new vision for postpartum care will narrow gaps in important maternal child health outcomes.
Women of lower socioeconomic status are at significantly increased risk of unintended pregnancies, short inter-pregnancy interval and short duration of breastfeeding. The consequences of untimed pregnancies and short duration of breastfeeding for the health of mothers, infants and children are well documented. In addition to significant health implications, these inequalities have important economic ramifications. The cost of births from unintended pregnancies in 2006 was estimated at $11 billion in maternity and infant care. This does not include cost of abortion care, lost productivity, and government assistance.
Providers have effective postpartum strategies to reduce the risk of poorly timed pregnancies and low breastfeeding rates.
Short interval or poorly timed pregnancies: Women have a range of effective contraceptive options, however, not initiating contraception postpartum remains common. The provision of long-acting reversible contraception (LARC) including intrauterine devices (IUDs) and hormonal implants has been shown to decrease short interval pregnancies and the associated risk of preterm birth. Importantly, given the array of contraceptive options available to women, it is important to make LARC accessible while empowering women to choose a method that is effective and acceptable to them. This highlights the need for solutions to engage women in patient centered comprehensive contraceptive decision-making in the postpartum period.
Short Breastfeeding Duration: A number of strategies have been shown to increase breastfeeding success. Most relevant to our proposal is that efforts to educate women about the benefits of breastfeeding, weekly text reminders in the immediate postpartum period, and access to a lactation consultant have all improved both duration and exclusivity of breastfeeding. Importantly, three recent trials demonstrated significant increases in exclusive breastfeeding from eight weeks to six months postpartum among women who received weekly-automated text message breastfeeding support. These interventions may be particularly relevant to our target population, as low-income, non-Hispanic Black women between 18-29 years send and receive text messages more frequently than any other demographic.
There are important high-risk subgroups of women who benefit uniquely from postpartum care given the need to link these women to primary or specialty health care providers in postpartum period.
Gestational diabetes (GDM): GDM complicates roughly 6-9% of pregnancies, but disproportionately burdens those with lower socio-economic status. Women with GDM are at increased risk of type 2 diabetes, metabolic syndrome, and cardiovascular disease after delivery. These findings are present as early as 3 months postpartum with the absolute risk of Type 2 diabetes approaching 5% a year postpartum. Professional societies recommend screening women for diabetes 4-12 weeks after delivery and linking women to primary care to improve long-term maternal health. In 2016, only 14% of economically disadvantaged women who received prenatal care at the Magee-Womens Hospital outpatient clinic returned for their postpartum screening. This is slightly better than national trends, which suggest roughly 6% of women with GDM had recommend postpartum screening and 13.8% had a primary care visit within a year.
Hypertensive disorders of pregnancy: Hypertensive disorders of pregnancy occur in roughly 6-8% of pregnancies and low SES is an independent risk factor. Women with hypertensive disorders of pregnancy, either gestational hypertension or preeclampsia, are more than twice as likely to develop hypertension or prehypertension in the 12 months after delivery. They are also at increased risk for cardiovascular disease. Given this, women with a hypertensive disorder of pregnancy should have early postpartum follow up for a blood pressure and establish care with a primary care physician within a year of delivery.
Recognizing the importance of the postpartum period for the health of women and children across their lifespans, ACOG recently proposed a new paradigm for postpartum care. In their new vision for postpartum care ACOG emphasized the following: 1) Postpartum care should be an on-going process rather than a single encounter 2) The content of postpartum care should be tailored to a woman's individual needs 3) The timing of the postpartum visit should be individualized for a woman. How to implement and scale this model of postpartum care and whether it will improve health outcomes for women and children has not been investigated.
Despite considerable maternal morbidity and mortality in the postpartum period, attendance rates for the postpartum visit are markedly lower for women with limited resources contributing to economic health disparities. While women with Medicaid receive excellent prenatal care, only 50% of them return for their postpartum visit. These parallel national trends, where 60% of women with Medicaid insurance return for a postpartum checkup compared with over 82% of women with private insurance. Medicaid programs serve pregnant women who are particularly vulnerable to poor health outcomes and thus this gap is critical. These data demonstrate that our current care model does not engage all women in quality postpartum care and is disproportionately failing our most vulnerable moms and babies.
Existing interventions to improve adherence with the postpartum visit have not been rigorously evaluated, would be difficult to scale, and do not reflect the new vision for postpartum care outlined by ACOG.
Empirically derived concepts from behavioral economics can be leveraged to design interventions that support patient's engagement in their health. The field of behavioral economics acknowledges that people do not make exclusively rational choices. In fact, immediate (rather than future) needs, cognitive and psychological biases, and social norms profoundly influence decision-making. Insights from the field of behavioral economics have begun to influence the health sciences as researchers seek more effective health interventions and health policy.
Healthy Beyond Pregnancy incorporates tenets of behavioral economics that address two powerful drivers of behavioral change-- awareness and willingness. Awareness has three parts: 1) an awareness of how one's behavior affects oneself 2) an awareness of how one's actions impact others and 3) an awareness of social norms around the given behavior. Awareness alone, however, is insufficient to alter behavior. People must be willing to change their behavior. Designing health interventions that address both awareness and willingness are more likely to lead to behavior change.
In the current proposal the investigators focus on four tenets of behavioral economics-bounded rationality (information overload), status quo bias (valuing the present self over the future self), hovering (limited attention), and framed incentives-- that address both awareness and willingness and have been successfully used to tackle stubborn health problems such as smoking and obesity. Both bounded rationality and hovering address awareness, while status quo bias and framed incentives address willingness.
In summary, this proposal is significant because it will evaluate the impact of an innovative program built on empirically derived concepts of behavioral economics on health decision-making in the postpartum period- a critical window for maternal child health. Our program directly mirrors the new vision for postpartum care outlined by ACOG. Additionally, it targets low-income women who are at risk for not participating in postpartum care to promote equality in maternal child health.
- Conditions
- Postpartum Care
- Being tested
- Healthy Beyond Pregnancy, Pre-Scheduled Postpartum Visit, Attention Control
- Keywords
- contraception, postpartum care, breast feeding, interconception care
- Medical subject headings
- Breast Feeding
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Healthy Beyond PregnancyBehavioural
Web-based application grounded in tenants of behavioral economics.
Pre-Scheduled Postpartum VisitBehavioural
Participants will have their postpartum visit scheduled while they are still in the hospital after delivery.
Attention ControlOther
Participants will receive texts related to infant care to mirror the attention participants receive in the Healthy Beyond Pregnancy intervention.
| Study group | Role | What they receive |
|---|---|---|
| Attention Control Group | Active comparator | If randomized to the attention control arm participants will receive discharge instruction from the postpartum nurses per usual care. Study investigators will ask them to provide us with an SMS number. This will enable collection of self-reported breast feeding duration as well as texts on general infant care. The infant care texts are educational in nature and no data will be collected. Participants will receive a total of two texts on general infant care in the first month postpartum. This increased attention to the control arm mirrors the attention received by the Healthy Beyond Pregnancy arms and seeks to isolate the effect of the intervention from a general increased level of contact with providers. Receives: Other: Attention Control |
| Pre-Scheduled Postpartum Visit: | Active comparator | If randomized the usual care with pre-scheduled visit arm, participants will schedule their postpartum visit with the study coordinator and receive discharge information per usual care. Receives: Behavioral: Pre-Scheduled Postpartum Visit |
| Healthy Beyond Pregnancy | Experimental | Healthy Beyond Pregnancy is a web platform with an electronic survey that assesses a participant's self-identified postpartum concerns. Participants are then presented with 3 educational videos that reflect their self-identified needs from the survey. The Healthy Beyond Pregnancy generates an individualized passport for postpartum care. This passport for care lists the women's self-identified postpartum needs as well as issues that should be prioritized based on her health history. The individualized passport for postpartum care will be printed out and given to participants. After the participant schedules her postpartum visit, she will receive a printout that includes the date and time of her appointment, a copy of the commitment statement. Receives: Behavioral: Healthy Beyond Pregnancy |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of Participants Using a Non-barrier Method of Contraception
Effective contraception (non-barrier method)
Measured: 3 months after delivery
Number of Participants Using a Non-barrier Method of Contraception
Effective contraception (non-barrier method)
Measured: 6 months after delivery
Adherence of Postpartum Visit
Attendance at postpartum visit (yes/no)
Measured: 12 weeks after deliery
Secondary outcomes (4)
The Number of Participants Who Given Their Infant Breast Milk
Rates of breast feeding
Measured: 1 week after delivery
The Number of Participants Who Given Their Infant Breast Milk
Rates of breast feeding
Measured: 1 month after delivery
The Number of Participants Who Given Their Infant Breast Milk
Rates of breast feeding
Measured: 3 months after delivery
The Number of Participants Who Given Their Infant Breast Milk
Rates of breast feeding
Measured: 6 months after delivery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Feb 2020
- Study start3 Feb 2020
- Primary completion2 Jun 2021
- Study completion2 Sep 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Postpartum CareStudies of the same condition, open and under way.
- More trials run by University of PittsburghThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Investigator
- Enrolment
- 128 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Pittsburgh
- Sponsor type
- University, hospital or other
- Collaborators
- National Institute of Nursing Research (NINR)
- Responsible party
- Principal investigator, Katherine Himes, University of Pittsburgh
- Investigators
- Francesca Facco, MD, Principal investigator, University of Pittsburgh
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04257552
- Sponsor's protocol ID
- STUDY19040312
- Other IDs
- 1R56NR017933-01A1
- Acronym
- CAPS
- Status last verified
- Sep 2022
- First submitted
- 31 Jan 2020
- Last updated
- 21 Oct 2022
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: All of the individual participant data collected during the trail will be shared immediately after publication of the trial. Data can be obtained by contacting central contact person, Katherine Himes at himekp@upmc.edu.
Study at a glance
From the registry record, last updated by the sponsor on 21 Oct 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Care After Pregnancy Study (CAPS): Randomized Controlled Trial of Patient Engagement After Pregnancy
- ClinicalTrials.gov ID
- NCT04257552
- Acronym / sponsor ID
- CAPS / STUDY19040312
- Conditions
- Postpartum Care
- Keywords
- contraception, postpartum care, breast feeding, interconception care
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 128 participants (actual)
- Lead sponsor
- University of PittsburghUniversity, hospital or other
- Collaborators
- National Institute of Nursing Research (NINR)
- Study start
- 3 Feb 2020 (actual)
- Primary completion
- 2 Jun 2021 (actual)
- Study completion
- 2 Sep 2021 (actual)
- First posted
- 6 Feb 2020 (actual)
- Results
- Posted 21 Oct 2022
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The overarching hypothesis of our research agenda is that an intervention that engages economically disadvantaged women in personalized postpartum care will promote equality in maternal child health. As a first step to test our hypothesis the investigators propose the following aims:
Specific Aim 1: Measure the impact of Healthy Beyond Pregnancy on key components of postpartum care, including use of effective contraception at three and six months postpartum and breastfeeding duration at three and six months.
Specific Aim 2: Determine if Healthy Beyond Pregnancy improves adherence to health screening and linkage to follow-up care for women with cardio-metabolic complications of pregnancy.
Detailed description
There are profound economic inequalities in a wide range of important maternal and child health outcomes ranging from neonatal death to maternal morbidity and mortality. The overarching scientific premise for our proposal is that these inequalities stem in part from poor engagement in postpartum care by economically disadvantaged women. The investigators hypothesize that an innovative intervention grounded in empirically derived tenets of behavioral economics that includes the critical components of the American College of Obstetricians and Gynecologists (ACOG) new vision for postpartum care will narrow gaps in important maternal child health outcomes.
Women of lower socioeconomic status are at significantly increased risk of unintended pregnancies, short inter-pregnancy interval and short duration of breastfeeding. The consequences of untimed pregnancies and short duration of breastfeeding for the health of mothers, infants and children are well documented. In addition to significant health implications, these inequalities have important economic ramifications. The cost of births from unintended pregnancies in 2006 was estimated at $11 billion in maternity and infant care. This does not include cost of abortion care, lost productivity, and government assistance.
Providers have effective postpartum strategies to reduce the risk of poorly timed pregnancies and low breastfeeding rates.
Short interval or poorly timed pregnancies: Women have a range of effective contraceptive options, however, not initiating contraception postpartum remains common. The provision of long-acting reversible contraception (LARC) including intrauterine devices (IUDs) and hormonal implants has been shown to decrease short interval pregnancies and the associated risk of preterm birth. Importantly, given the array of contraceptive options available to women, it is important to make LARC accessible while empowering women to choose a method that is effective and acceptable to them. This highlights the need for solutions to engage women in patient centered comprehensive contraceptive decision-making in the postpartum period.
Short Breastfeeding Duration: A number of strategies have been shown to increase breastfeeding success. Most relevant to our proposal is that efforts to educate women about the benefits of breastfeeding, weekly text reminders in the immediate postpartum period, and access to a lactation consultant have all improved both duration and exclusivity of breastfeeding. Importantly, three recent trials demonstrated significant increases in exclusive breastfeeding from eight weeks to six months postpartum among women who received weekly-automated text message breastfeeding support. These interventions may be particularly relevant to our target population, as low-income, non-Hispanic Black women between 18-29 years send and receive text messages more frequently than any other demographic.
There are important high-risk subgroups of women who benefit uniquely from postpartum care given the need to link these women to primary or specialty health care providers in postpartum period.
Gestational diabetes (GDM): GDM complicates roughly 6-9% of pregnancies, but disproportionately burdens those with lower socio-economic status. Women with GDM are at increased risk of type 2 diabetes, metabolic syndrome, and cardiovascular disease after delivery. These findings are present as early as 3 months postpartum with the absolute risk of Type 2 diabetes approaching 5% a year postpartum. Professional societies recommend screening women for diabetes 4-12 weeks after delivery and linking women to primary care to improve long-term maternal health. In 2016, only 14% of economically disadvantaged women who received prenatal care at the Magee-Womens Hospital outpatient clinic returned for their postpartum screening. This is slightly better than national trends, which suggest roughly 6% of women with GDM had recommend postpartum screening and 13.8% had a primary care visit within a year.
Hypertensive disorders of pregnancy: Hypertensive disorders of pregnancy occur in roughly 6-8% of pregnancies and low SES is an independent risk factor. Women with hypertensive disorders of pregnancy, either gestational hypertension or preeclampsia, are more than twice as likely to develop hypertension or prehypertension in the 12 months after delivery. They are also at increased risk for cardiovascular disease. Given this, women with a hypertensive disorder of pregnancy should have early postpartum follow up for a blood pressure and establish care with a primary care physician within a year of delivery.
Recognizing the importance of the postpartum period for the health of women and children across their lifespans, ACOG recently proposed a new paradigm for postpartum care. In their new vision for postpartum care ACOG emphasized the following: 1) Postpartum care should be an on-going process rather than a single encounter 2) The content of postpartum care should be tailored to a woman's individual needs 3) The timing of the postpartum visit should be individualized for a woman. How to implement and scale this model of postpartum care and whether it will improve health outcomes for women and children has not been investigated.
Despite considerable maternal morbidity and mortality in the postpartum period, attendance rates for the postpartum visit are markedly lower for women with limited resources contributing to economic health disparities. While women with Medicaid receive excellent prenatal care, only 50% of them return for their postpartum visit. These parallel national trends, where 60% of women with Medicaid insurance return for a postpartum checkup compared with over 82% of women with private insurance. Medicaid programs serve pregnant women who are particularly vulnerable to poor health outcomes and thus this gap is critical. These data demonstrate that our current care model does not engage all women in quality postpartum care and is disproportionately failing our most vulnerable moms and babies.
Existing interventions to improve adherence with the postpartum visit have not been rigorously evaluated, would be difficult to scale, and do not reflect the new vision for postpartum care outlined by ACOG.
Empirically derived concepts from behavioral economics can be leveraged to design interventions that support patient's engagement in their health. The field of behavioral economics acknowledges that people do not make exclusively rational choices. In fact, immediate (rather than future) needs, cognitive and psychological biases, and social norms profoundly influence decision-making. Insights from the field of behavioral economics have begun to influence the health sciences as researchers seek more effective health interventions and health policy.
Healthy Beyond Pregnancy incorporates tenets of behavioral economics that address two powerful drivers of behavioral change-- awareness and willingness. Awareness has three parts: 1) an awareness of how one's behavior affects oneself 2) an awareness of how one's actions impact others and 3) an awareness of social norms around the given behavior. Awareness alone, however, is insufficient to alter behavior. People must be willing to change their behavior. Designing health interventions that address both awareness and willingness are more likely to lead to behavior change.
In the current proposal the investigators focus on four tenets of behavioral economics-bounded rationality (information overload), status quo bias (valuing the present self over the future self), hovering (limited attention), and framed incentives-- that address both awareness and willingness and have been successfully used to tackle stubborn health problems such as smoking and obesity. Both bounded rationality and hovering address awareness, while status quo bias and framed incentives address willingness.
In summary, this proposal is significant because it will evaluate the impact of an innovative program built on empirically derived concepts of behavioral economics on health decision-making in the postpartum period- a critical window for maternal child health. Our program directly mirrors the new vision for postpartum care outlined by ACOG. Additionally, it targets low-income women who are at risk for not participating in postpartum care to promote equality in maternal child health.
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (investigator)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Attention Control Group | Active comparator | Other: Attention ControlIf randomized to the attention control arm participants will receive discharge instruction from the postpartum nurses per usual care. Study investigators will ask them to provide us with an SMS number. This will enable collection of self-reported breast feeding duration as well as texts on general infant care. The infant care texts are educational in nature and no data will be collected. Participants will receive a total of two texts on general infant care in the first month postpartum. This increased attention to the control arm mirrors the attention received by the Healthy Beyond Pregnancy arms and seeks to isolate the effect of the intervention from a general increased level of contact with providers. |
| Pre-Scheduled Postpartum Visit: | Active comparator | Behavioral: Pre-Scheduled Postpartum VisitIf randomized the usual care with pre-scheduled visit arm, participants will schedule their postpartum visit with the study coordinator and receive discharge information per usual care. |
| Healthy Beyond Pregnancy | Experimental | Behavioral: Healthy Beyond PregnancyHealthy Beyond Pregnancy is a web platform with an electronic survey that assesses a participant's self-identified postpartum concerns. Participants are then presented with 3 educational videos that reflect their self-identified needs from the survey. The Healthy Beyond Pregnancy generates an individualized passport for postpartum care. This passport for care lists the women's self-identified postpartum needs as well as issues that should be prioritized based on her health history. The individualized passport for postpartum care will be printed out and given to participants. After the participant schedules her postpartum visit, she will receive a printout that includes the date and time of her appointment, a copy of the commitment statement. |
Who may qualify
- Ages
- 12 to 50 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
Key inclusion criteria (2 listed)
- Insured by a PA Medicaid insurance
- Pregnancy care in the Magee Womens Hospital Outpatient Clinic
Key exclusion criteria (4 listed)
- Delivery less than 24 weeks
- Fetal or neonatal demise
- Women who had a postpartum tubal ligation
- Women less than 18 year of age
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Healthy Beyond PregnancyWeb-based application grounded in tenants of behavioral economics. | Behavioural | Healthy Beyond Pregnancy |
| Pre-Scheduled Postpartum VisitParticipants will have their postpartum visit scheduled while they are still in the hospital after delivery. | Behavioural | Pre-Scheduled Postpartum Visit: |
| Attention ControlParticipants will receive texts related to infant care to mirror the attention participants receive in the Healthy Beyond Pregnancy intervention. | Other | Attention Control Group |
Primary outcome
Number of Participants Using a Non-barrier Method of Contraception
Time frame: 3 months after delivery
Effective contraception (non-barrier method)
Number of Participants Using a Non-barrier Method of Contraception
Time frame: 6 months after delivery
Effective contraception (non-barrier method)
Adherence of Postpartum Visit
Time frame: 12 weeks after deliery
Attendance at postpartum visit (yes/no)
4 secondary outcomes
The Number of Participants Who Given Their Infant Breast Milk
Time frame: 1 week after delivery
The Number of Participants Who Given Their Infant Breast Milk
Time frame: 1 month after delivery
The Number of Participants Who Given Their Infant Breast Milk
Time frame: 3 months after delivery
The Number of Participants Who Given Their Infant Breast Milk
Time frame: 6 months after delivery
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Oct 2022.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Individual participant dataSharing planned: Yes. All of the individual participant data collected during the trail will be shared immediately after publication of the trial. Data can be obtained by contacting central contact person, Katherine Himes at himekp@upmc.edu.
Related trials for Postpartum Care
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Effectiveness Study of a Lifestyle Intervention Versus Metformin in Mothers With Recent Gestational Diabetes
Weight Loss, Gestational Diabetes Mellitus in Pregnancy
RecruitingPhase 4
Optimizing Preeclampsia Postpartum With Point-of-care Ultrasound
Preeclampsia, Preeclampsia Postpartum
Not yet recruiting
Community Support and Mobile Apps to Help Black Women Control High Blood Pressure After Pregnancy
Hypertensive Disorders of Pregnancy (HDP), Hypertension, Pregnancy Induced
Recruiting
Early Intervention for Postpartum PTSD: Comparing Written Exposure and Capnometry-Guided Breathing Therapy
Written Exposure Therapy, Breathing Techniques
Recruiting
Community Health Worker Support to Lower Blood Pressure After a Pregnancy With High Blood Pressure
Pregnancy-Associated Hypertension, Gestational Hypertension
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Francesca Facco, MD principal investigator
University of Pittsburgh
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Healthy Beyond Pregnancy and Pre-Scheduled Postpartum Visit in people with Postpartum Care, run by University of Pittsburgh at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 21 Oct 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Yes. Results are posted in the registry (first posted 21 Oct 2022). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of Participants Using a Non-barrier Method of Contraception (time frame: 3 months after delivery). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Oct 2022.