Intensive Education
OtherIntervention will consist of virtual education and communication through scheduled push notifications
NCT Number: NCT06218355
The purpose of this study is to compare two complex, multi-component evidence-based postpartum interventions in underserved populations of lower socioeconomic status in an effort to reduce maternal morbidity and mortality.
Interested in participating?
Request Info18 year and older
Female
Interventional
Not applicable
Emory University School of Medicine, Atlanta, Georgia, United States
This large, multi-center randomized controlled trial will compare two multi-component postpartum care models via hybrid type 1 design conducted in two phases. An initial phase (phase 1) will collect baseline data and ensure patient input into final study. In phase 2, women will be randomized. Comparators are evidenced- based approaches: (1) an intensive in-person education with virtual education via push notifications using an electronic health record web portal; (2) a telehealth model using serial encounters. The "push" approach using notifications directly contrasts with the "pull" approach using telehealth visits. Both models include home visit programs. The study population includes patients delivering in two urban, inner-city health systems: Parkland (Dallas, TX) and Grady Memorial (Atlanta, GA). The primary outcome is time from hospital discharge to diagnosis and treatment of a composite of complications in the first 6 weeks. Based upon pilot data, 2349 women will demonstrate a 40% reduction (9 to 5.4 days) with 80% power and two-sided alpha of 0.05. 3500 women will be enrolled (1000 in phase 1; 2500 in phase 2) with anticipated <5% attrition at 6 weeks. Inclusion will be women who deliver liveborn infants. Secondary outcomes include mental health disorders, emergency room visits, hospital admissions, patient knowledge, quality of life and satisfaction, provider satisfaction, and social determinants of health. Women will be followed for one year postpartum.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Intervention will consist of virtual education and communication through scheduled push notifications
Intervention will utilize a telehealth model consisting of "pull" approach of patient engagement.
Time frame: Up to one year postpartum
Time to diagnosis and treatment of postpartum complications including hypertension, wound infection, and venous thromboembolism, measured in days. Lower value is considered better, representing timely care.
Time frame: enrollment, 1 week, 6 weeks, 3 months, 6 months, 1 year postpartum
screening continuous, numerical; higher value consistent with great risk of postpartum depression
Time frame: enrollment, 1 week, 6 weeks, 3 months, 6 months, 1 year postpartum
screening tool, continuous, numerical, higher value consistent with higher risk of anxiety disorder
Time frame: Up to one year postpartum
continuous variable, preventability to be determined by preventability panel
Time frame: Up to one year postpartum
continuous variable, preventability to be determined by preventability panel
Time frame: enrollment, 1 week, 6 weeks, 3 months, 6 months, 1 year postpartum
Percent scored correct out of 10 total questions
Time frame: 6 weeks and 1 year postpartum
Scales 1-10 for each independent question, with numerical summary score
Time frame: 6 weeks and 1 year postpartum
categorical variables selected by the participant
Time frame: 6 weeks and 1 year postpartum
categorical and dichotomous variables
Time frame: 6 weeks and 1 year postpartum
Scale: Extremely dissatisfied to extremely satisfied Score Range is 0-28.
Time frame: Every 6 months throughout the study period
Scale: Strong agree to strongly disagree; very good to very bad; often to never
Time frame: enrollment, 1 week, 6 weeks, 3 months, 6 months, 1 year postpartum
numerical, continuous
Time frame: enrollment, 1 week, 6 weeks, 3 months, 6 months, 1 year postpartum
numerical, continuous
Time frame: enrollment, 6 weeks, 1 year postpartum
qualitative data, each questions treated as dichotomous or categorical variables
Time frame: enrollment, 6 weeks, 3 months, and 1 year postpartum
laboratory value - continuous variables
Time frame: enrollment, 6 weeks, 3 months, and 1 year postpartum
laboratory value - continuous variable
Time frame: enrollment, 6 weeks, 3 months, and 1 year postpartum
laboratory value - continuous variables
Time frame: enrollment, 6 weeks, 3 months, and 1 year postpartum
laboratory value - continuous variables
Contact information is provided by the study sponsor or research team.
Jacqueline Catchings, PhD
CONTACT
Lisa Moseley, RN
CONTACT
University of Texas Southwestern Medical Center
Other
Acronym: IMPACT
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.
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