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Behavioural Intervention
Postpartum Follow-Up Card for Enhancing Postpartum Care
N/A
Recruiting
Research Sponsored by Medstar Health Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Subjects >=18 years of age
Delivered via vaginal delivery or c-section within the past 48 hours
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
Study Summary
This trial will test if postpartum cards with patient's name & tasks will help them complete postpartum health tasks more often.
Who is the study for?
This trial is for individuals who are at least 18 years old, can consent for themselves, and can read English or Spanish. They must have delivered a baby via vaginal delivery or c-section within the past 48 hours at a Medstar facility and plan to continue their care within the same system.Check my eligibility
What is being tested?
The study tests if personalized postpartum follow-up cards given at discharge improve completion of health tasks like blood pressure checks and glucose tolerance tests. Participants will be randomly assigned to receive either this card with tailored appointments or standard education provided upon discharge.See study design
What are the potential side effects?
Since this trial involves non-medical interventions (follow-up cards), there are no direct medical side effects associated with it. However, participants may experience stress or anxiety related to following up on their healthcare tasks.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 years old or older.
Select...
I gave birth in the last 48 hours.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Blood pressure check
Two hour glucose tolerance test
Secondary outcome measures
Cervical cancer screening
Primary care
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Follow up cardsExperimental Treatment1 Intervention
Subjects will receive a personalized postpartum health card with recommendations for follow up based on their comorbid conditions in pregnancy. They will receive education about these comorbid conditions when they receive their cards.
Group II: Standard educationPlacebo Group1 Intervention
Subjects will receive standard postpartum education as it is routinely performed by nurses prior to discharge.
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Who is running the clinical trial?
Medstar Health Research InstituteLead Sponsor
189 Previous Clinical Trials
115,333 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
How many participants are allowed to join this clinical trial?
"Affirmative. According to details on clinicaltrials.gov, this medical research project has been accepting participants since May 22nd 2023 and is still recruiting now. A total of 240 individuals need to be recruited from a single site."
Answered by AI
Is this research endeavor still open to recruitment?
"Data hosted on clinicaltrials.gov suggests that this medical research is still open to participants, with the trial initially posted on May 22nd 2023 and last updated September 19th of the same year."
Answered by AI
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