A Pharmacist Intervention to Improve Mother and Child Health
- Conditions
- Hypertension
- Registration Number
- NCT06073054
- Lead Sponsor
- University of Iowa
- Brief Summary
The goal of this clinical trial is to learn if a research pharmacist can improve the health of new mothers and their babies. The main questions it aims to answer are:
* Will postpartum women who had elevated blood pressure during pregnancy be willing to participate in the study, talk to a pharmacist about their health and the health of their child, and text us their blood pressure measurements?
* Will contact with the pharmacist improve the health of the mother and/or the child?
Participants will:
* complete a baseline demographic survey,
* be given a blood pressure cuff and taught how to use it,
* be asked to text us their blood pressure values 2 times per day for 7 days after enrollment,
* complete a phone call with a pharmacist discussing their health and the health of their baby,
* text us their blood pressure 1 time per day for 3 days 1 month after enrollment,
* have a 1 month follow-up phone call with the research pharmacist, and
* complete an exit survey to provide feedback about the study.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 25
- biological mother of a baby attending a 1-week to 6-month well-child visit,
- received prenatal care at University of Iowa Hospitals and Clinics,
- had at least 2 elevated blood pressures (>= 130 mmHg systolic or >= 80 mmHg diastolic) during pregnancy,
- owns a smartphone
- arm circumference > 17 inches,
- prisoner status
- unable to provide own written informed consent
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Number of Participants Who Talk to Research Pharmacist Through study completion, an average of 30 days We will calculate the number of participants who talk to the research pharmacist during the course of the intervention.
Number of Participants Who Return BP Measurements Through study completion, an average of 30 days We will calculate the number of participants who return at least one blood pressure measurement via text message.
Percentage of Well-Child Visits Attended Through study completion, an average of 30 days We will calculate the percentage of well-child visits that are attended by each family.
Percentage of Vaccinations Received Through study completion, an average of 30 days We will calculate the percentage of vaccinations received by each child.
- Secondary Outcome Measures
Name Time Method Number of BP Measurements Submitted Through study completion, an average of 30 days We will calculate the number of blood pressure values that are submitted by each participant.
Blood Pressure Control Through study completion, an average of 30 days We will determine how many participants' blood pressure is controlled after the intervention.
Number of Participants Satisfied With the Study Through study completion, an average of 30 days We will measure participant satisfaction with the study using an exit survey. Satisfaction will be measured by a response of Extremely Helpful or Helpful on the question- My contact(s) with the pharmacist about my health were....
Trial Locations
- Locations (1)
University of Iowa Hospitals and Clinics
🇺🇸Iowa City, Iowa, United States
University of Iowa Hospitals and Clinics🇺🇸Iowa City, Iowa, United States