Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03242174
Other study ID # PBRC 2017-036
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 11, 2017
Est. completion date June 2024

Study information

Verified date August 2023
Source Pennington Biomedical Research Center
Contact Abby D. Altazan, M.S.
Phone 2257632801
Email abby.duhe@pbrc.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To assess health and lifestyle behavior of pregnant women in Baton Rouge including women receiving traditional obstetrical prenatal care and delivering in a hospital and those receiving prenatal care from a midwife and delivering at the birth center.


Description:

It is of scientific interest to learn what the health and lifestyle behaviors are for women receiving prenatal care in a non-traditional birth center and the impact of these behaviors on pregnancy and birth outcomes.Participants will be offered a questionnaire packet to complete at a prenatal appointment in the third trimester of pregnancy by their obstetrical prenatal care provider. The questionnaire packet will take approximately 10-15 minutes to complete.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date June 2024
Est. primary completion date June 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - Pregnant women in the third trimester of pregnancy = 28 weeks GA Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Health Behavior Questionnaire Packet
Any pregnant woman offered the questionnaire at her prenatal appointment in the third trimester can complete

Locations

Country Name City State
United States Pennington Biomedical Research Center Baton Rouge Louisiana

Sponsors (1)

Lead Sponsor Collaborator
Pennington Biomedical Research Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Eating Habits Eating Habits assessed by Eating Habits Questionnaire 1 Day
Primary Eating Habits Eating Habits assessed by Rapid Eating Assessment for Participants-Shortened Version 1 Day
Primary Mindful Eating Mindful Eating assessed by Mindful Eating Questionnaire 1 Day
Primary Physical Activity Physical Activity assessed by Nurses Health Study II Physical Activity Questionnaire 1 Day
Primary Frequency of Weighing Frequency of Weighing by Frequency of Weighing Questionnaire 1 Day
Primary Sedentary Behavior Sedentary Behavior by Sedentary Behavior Questionnaire 1 Day
Primary Functional health and well-being Quality of life measure that assesses functional health and well-being from the participant's point of view by 12 Item Short Form Health Survey by RAND 1 Day
Primary Sleep Habits Sleep Habits by Sleep Questionnaire 1 Day
See also
  Status Clinical Trial Phase
Completed NCT05017974 - Research on Improving Sleep During Pregnancy N/A
Completed NCT03284515 - Vaccination In Pregnancy Gene Signature: VIP Signature Study
Recruiting NCT05969795 - Comparison of Live Birth Rate in Natural Cycle Single Euploid FET Versus Without Luteal Phase Support Phase 1
Recruiting NCT06051201 - Innovation for Small-scale Experiments: ReceptIVFity Test N/A
Recruiting NCT04828382 - Prospective Study of Pregnancy in Women With Cystic Fibrosis
Enrolling by invitation NCT04527926 - STEPuP: Prenatal Provider Education and Training to Improve Medication-assisted Treatment Use During Pregnancy N/A
Recruiting NCT04278651 - Early Antenatal Support for Iron Deficiency Anemia Phase 4
Recruiting NCT04405700 - Measuring Adverse Pregnancy and Newborn Congenital Outcomes
Recruiting NCT06258902 - Odevixibat Pregnancy and Lactation Surveillance Program: A Study to Evaluate the Safety of Odevixibat During Pregnancy and/or Lactation
Completed NCT05487196 - Effectiveness of Clonidine, Dexmedetomidine, and Fentanyl Adjuncts for Labor Epidural Analgesia Phase 2
Completed NCT03750968 - Lutein & Zeaxanthin in Pregnancy - Carotenoid Supplementation During Pregnancy: Ocular and Systemic Effects Phase 2
Enrolling by invitation NCT06127277 - Next4You: A Fully Mobile Relationships Based Program for Youth in Foster Care N/A
Completed NCT05897697 - Assessing Women's Preferences for Postpartum Thromboprophylaxis: the Prefer-Postpartum Study
Recruiting NCT05899101 - The Impact of Opioid and Cannabis Exposure on Fetal Growth
Completed NCT05502510 - Assessing the Effectiveness and Efficacy of the MyHealthyPregnancy Application
Completed NCT04296396 - Opioid Prescription After Cesarean Trial Phase 3
Not yet recruiting NCT06069856 - Multiple Micronutrient Supplementation (MMS) IFA- Iron Dose Acceptability Crossover Trial Phase 3
Not yet recruiting NCT06069869 - Multiple Micronutrient Supplementation (MMS) Iron Dose Acceptability Crossover Trial Phase 3
Not yet recruiting NCT06163651 - Evaluating a One-Year Version of the Parent-Child Assistance Program N/A
Not yet recruiting NCT06079918 - Multiple Micronutrient Supplementation for Maternal Anemia Prevention in Tanzania Phase 3