Quarenta Semanas: Innovative Intervention in Prenatal Care for Reduction of Prematurity (quarenta)
Primary Purpose
Pregnancy
Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
prenatal care in groups
Sponsored by
About this trial
This is an interventional prevention trial for Pregnancy focused on measuring prenatal care, pregnancy, prematurity
Eligibility Criteria
Inclusion Criteria:
In order to be eligible to participate in this study:
- women must be at least eighteen years old and pregnant.
- They must be less than 12 weeks pregnant at the time of enrollment.
- They must speak Portuguese.
- Multiple gestation pregnancies will be excluded.
Exclusion Criteria:
- women who submit reasons not to take part groups after applying the questionnaire
Sites / Locations
- Maria Elisabeth Moreira
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Prenatal Care in groups
Control Group
Arm Description
We will do prenatal care using centering care pregnancy methodology in 10 sessions
We will do in this arm conventional Prenatal care available in the family clinics
Outcomes
Primary Outcome Measures
prematurity rate
birth before 37 weeks of gestational age
Secondary Outcome Measures
mothers satisfaction
scale to do measurement of mothers satisfaction
vaginal birth
% of normal birth
Full Information
NCT ID
NCT02506725
First Posted
July 20, 2015
Last Updated
August 26, 2019
Sponsor
Oswaldo Cruz Foundation
Collaborators
Montefiore Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT02506725
Brief Title
Quarenta Semanas: Innovative Intervention in Prenatal Care for Reduction of Prematurity
Acronym
quarenta
Official Title
Quarenta Semanas: Innovative Intervention in Prenatal Care for Reduction of Prematurity
Study Type
Interventional
2. Study Status
Record Verification Date
July 2019
Overall Recruitment Status
Unknown status
Study Start Date
August 2015 (Actual)
Primary Completion Date
September 1, 2019 (Anticipated)
Study Completion Date
December 31, 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oswaldo Cruz Foundation
Collaborators
Montefiore Medical Center
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The goal of Quarenta Semanas is to remove risk factors for preterm birth by linking women to prenatal care in the first trimester; supporting, educating and empowering women in pregnancy to reduce maternal stress and interrupt social, psychological, attitudinal and biological risk factors for preterm birth; and providing evidence-based, quality care that identifies and intervenes medically to treat underlying chronic and emergent conditions associated with preterm birth.
Detailed Description
Brazil is among 10 countries with the highest rates of preterm birth (12.4%). Alarmingly, rates are rising. Research has identified multiple risk factors for preterm birth, which can be grouped into four domains, all of which must be addressed to result in meaningful reductions in preterm birth. Domain 1: Access to and utilization of prenatal care. With universal access to prenatal and postpartum care assured via Brazil's Stork Network, Community Health Workers will conduct neighborhood outreach to identify women early in pregnancy and assure that women use prenatal services in the first trimester.
Domain 2: Maternal social, demographic and attitudinal risk factors include maternal stress, lack on knowledge about pregnancy, lack of social support, feeling low control over their health and pregnancy care, unplanned or unwanted pregnancy, unsatisfactory relationship with the father, social isolation, and short interpregnancy interval. Maternal demographic characteristics (e.g., Black race, being single, maternal age under 21 or over 35 years, and poverty) are helpful for identifying high-risk women, but are less amenable to interventions to prevent preterm birth. Domain 3: Maternal physical health risk factors include prior preterm birth, multiple gestation, infection, mucosal or systemic immune responses, diabetes, under and overweight, and hypertension. Several of these factors may be prevented or treated with optimal medical care. Domain 4: Quality of prenatal care includes completing all prenatal care visits, provider compliance with prenatal care guidelines, access to recommended tests or equipment, and appropriate referral of high-risk pregnant women to specialty care. QS is designed to attenuate the effects of risk factors for preterm births in each of these four domains through early access to high quality prenatal care delivered in a group model. STUDY DESIGN The Randomized Trial Framework. We will implement QS in the context of a RCT. We recruited 4 clinics in the Stork Network that serve the same patient population and geographic area in the central and west area of Rio de Janeiro. We will pair them into 2 dyads matched by number of prenatal patients served. We will randomly assign one clinic in each dyad to implement QS and the other will continue to deliver care as usual. Below, when we describe activities related to QS, they will be done only in the 2 QS clinics; in the control clinics, we will collect data only. The clinics or Health Municipal Centers belong to the Municipal Health System. They are staffed by Family Doctors, Nurses and Health Agents and look after a specific geographic location. They provide prenatal care and are able to perform laboratory tests, X-rays and obstetrical ultrasonography. Clinics selected for this project follow at least 250 pregnant women per year. The 2 QS sites are intervention sites and two are control sites. All sites have WiFi or wired internet access for REDCap survey administration, which is web based. The targeted enrollment is 240 QS women, 20 groups of 12 women. In each of the two QS clinical sites, we will form one group per month for 10 months, totaling 20 groups. We will enroll an equivalent number of women in the control clinics matching the pace of recruitment in the QS clinics. We will track that the appropriate number of groups are started and that the meetings occur monthly from 16-32 weeks and then biweekly thereafter until delivery. The "Centering Care Pregnancy" methodology will be used in the intervention clinics in prenatal care in groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pregnancy
Keywords
prenatal care, pregnancy, prematurity
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
statistician and qualitative researchers
Allocation
Randomized
Enrollment
240 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Prenatal Care in groups
Arm Type
Experimental
Arm Description
We will do prenatal care using centering care pregnancy methodology in 10 sessions
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
We will do in this arm conventional Prenatal care available in the family clinics
Intervention Type
Other
Intervention Name(s)
prenatal care in groups
Other Intervention Name(s)
centering care for prenatal
Intervention Description
We will do prenatal care in groups using centering care pregnancy methodology
Primary Outcome Measure Information:
Title
prematurity rate
Description
birth before 37 weeks of gestational age
Time Frame
12 months
Secondary Outcome Measure Information:
Title
mothers satisfaction
Description
scale to do measurement of mothers satisfaction
Time Frame
12 months
Title
vaginal birth
Description
% of normal birth
Time Frame
12 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
In order to be eligible to participate in this study:
women must be at least eighteen years old and pregnant.
They must be less than 12 weeks pregnant at the time of enrollment.
They must speak Portuguese.
Multiple gestation pregnancies will be excluded.
Exclusion Criteria:
women who submit reasons not to take part groups after applying the questionnaire
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shioban Dolan, MD
Organizational Affiliation
Montefiore Medical Center
Official's Role
Study Director
Facility Information:
Facility Name
Maria Elisabeth Moreira
City
Rio de Janeiro
State/Province
RJ
ZIP/Postal Code
22250020
Country
Brazil
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Quarenta Semanas: Innovative Intervention in Prenatal Care for Reduction of Prematurity
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