- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06353113
Feasibility of a Prenatal Yoga Mobile App in African American Pregnant Women
Assessing the Feasibility of a Prenatal Mobile App in Pregnant African American Women: The Mindful Maternity Study
The goal of this research is to test if a prenatal yoga app can improve well-being in African American/Black (AA) pregnant women. The main questions it aims to answer are:
- Is the Down Dog prenatal yoga app feasible for AA pregnant women?
- How does mental and physical health change after using the Down Dog app for 12-weeks?
- What cultural adaptations to the Down Dog app are needed?
The study lasts for 12 weeks and participants are asked to:
- do prenatal yoga with the app for at least 20 min/day, three days/week, from home
- wear a Garmin Vivosmart 5 watch daily
- complete four online surveys
- complete an optional virtual interview
This project aims to advance public health by contributing to a broader understanding of how prenatal yoga can support the health and well-being of AA pregnant women and promote optimal maternal and child health outcomes.
Study Overview
Status
Intervention / Treatment
Detailed Description
Recruitment: The investigators will recruit 50 pregnant African American women from local prenatal clinics, non-profits, and social media.
Eligibility: All interested participants will complete a web-based eligibility screener (~5 minutes). Eligible participants will be asked to schedule a virtual intake appointment to review the consent form with a research team member.
Procedures: Participants must sign an informed consent and complete a Physical Activity Readiness Medical Examination (PARmed-X) for Pregnancy with their healthcare provider before beginning the study. Once participants sign the consent and return a completed PARmed-X form, they will be asked to schedule an in-person enrollment appointment.
During the in-person enrollment appointment, participants will receive a free yoga mat and Garmin Vivosmart 5, and study materials. A research team member will set up the Garmin device for the participant. Participants will be asked to resume normal activities for one week before beginning the intervention and to complete a baseline survey.
After one week of baseline data collection, a research team member will send the participant an email with instructions to download/use the prenatal yoga mobile app and other relevant study materials. Participants will then engage in prenatal yoga using the mobile app for at least 20 min/day, 3 days/week for the next 12 weeks. Participants will receive a mid-intervention survey at 6 weeks, a post-intervention survey at 12 weeks, and will have an opportunity to complete a virtual interview when the study is over. Within 1-2 weeks after the participants' due date, a research team member will send an online birth outcomes survey to collect self-reported birth outcomes.
The baseline, mid-intervention, and post-intervention surveys will ask about mental and physical health and perceptions about using the prenatal mobile app. The optional virtual interview will ask questions related to further understanding the feasibility of the prenatal yoga mobile app and exploring cultural adaptations to improve the app.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
-
San Diego, California, United States, 92182
- San Diego State University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria
Participants will be included in the study if they:
- Are 18-46 years of age (childbearing age)
- Reside in San Diego Metropolitan Area
- Speak English
- Are between 13-28 weeks when intervention starts
- Are primiparous (giving birth for the first time)
- Have a singleton pregnancy (pregnant with only one baby)
- Are yoga naive (<60 min/month for past 6 months)
- Have access to smartphone/mobile device
- Willing to wear a wrist worn fitness tracker for the duration of the study
- Willing to download and use 3 mobile apps for the duration of the study
- Identify as Black or African American
- Return a completed Physical Activity Readiness Medical Examination (PARmed-X) for Pregnancy form (HCP approves participation in prenatal PA program before beginning intervention)
Exclusion Criteria:
- High-risk pregnancy
- Severe psychiatric disorder or substance abuse
- Denial of physical activity participation from physician
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Down Dog Prenatal Yoga App
Prenatal yoga via Down Dog Prenatal Yoga Mobile App 20 minutes a day, 3 days per week, for 12 weeks.
|
The Down Dog prenatal yoga app launched in 2015 and was designed to align with the changes a pregnant body goes through in each trimester. Users can select a practice by trimester, which will offer modification cues to work with a changing body during pregnancy. Users can also customize their experience by boosting things like Heartburn or Pubic Symphysis so they can continue to practice yoga and omit poses that might be uncomfortable. The app also utilizes user feedback, to continuously implement new practices to better their app for user interface. All of the prenatal yoga classes were created by a certified and experienced prenatal yoga instructor who has a 200hr yoga certification through Pure Yoga (New York), 80hr prenatal yoga certification through Prenatal Yoga Center (New Yoga), and is Trauma Informed Yoga certified through Exhale to Inhale (New York). |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Acceptability of the intervention
Time Frame: Post intervention (12 weeks)
|
Assessed using an investigator-developed questionnaire using a 5 point likert scale from strongly agree to strongly disagree.
Acceptability benchmark: > 70% of participants report the intervention to be satisfactory, intend to continue using the app, and perceive the app content to be appropriate for pregnancy.
|
Post intervention (12 weeks)
|
|
Demand of the intervention
Time Frame: Assessed across 12-week study period
|
Assessed by measuring actual use of the mobile app with data analytics provided from Down dog.
Demand benchmark: >70% of participants complete at least 75% of their weekly prescribed minutes (i.e., ≥ 45 of 60 minutes per week).
|
Assessed across 12-week study period
|
|
Retention
Time Frame: Assessed across 12-week study period
|
Assessed by calculating the proportion of enrolled participants that complete intervention vs withdrawals.
Retention benchmark: ≥70% (N=35) complete the intervention.
|
Assessed across 12-week study period
|
|
Ease of recruitment
Time Frame: Assessed at enrollment
|
Assessed by evaluating enrollment rate.
Recruitment benchmark: >8 participants will be enrolled each month on average.
|
Assessed at enrollment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Discrimination
Time Frame: Baseline, Mid-intervention (6 weeks), and Post-intervention (12 weeks)
|
Discrimination will be assessed using the Discrimination in Medical Settings (DMS) Scale.
The DMS is a 7-item instrument scored on a 5-point Likert scale (1-never, 2-rarely, 3-sometimes, 4-most of the time, 5-always).
Higher scores indicate greater levels of discrimination.
|
Baseline, Mid-intervention (6 weeks), and Post-intervention (12 weeks)
|
|
Perceived stress
Time Frame: Baseline, Mid-intervention (6 weeks), and Post-intervention (12 weeks)
|
Perceived stress will be measured using the Perceived Stress Scale (PSS-10).
The PSS-10 is a 10-item instrument scored on a 5-point Likert scale (0-Never, 1- Almost Never, 2- Sometimes, 3- Fairly Often, 4-Very Often).
Higher scores indicate greater levels of perceived stress.
|
Baseline, Mid-intervention (6 weeks), and Post-intervention (12 weeks)
|
|
Perinatal Depression
Time Frame: Baseline, Mid-intervention (6 weeks), and Post-intervention (12 weeks)
|
Perinatal Depression will be measured using the 10-item Edinburg Postnatal Depression Scale (EPDS).
Scores range from 0-30, with "possible depression" defined by a score of 10 or greater.
|
Baseline, Mid-intervention (6 weeks), and Post-intervention (12 weeks)
|
|
Self-awareness
Time Frame: Baseline, Mid-intervention (6 weeks), and Post-intervention (12 weeks)
|
Self-awareness will be measured using the Self Awareness Outcomes Questionnaire (SAOQ).
The SAOQ is a 38-item instrument scored on a 5-point Likert scale (1- Never, 2- Rarely, 3- Occasionally, 4- Frequently, 5- Almost Always).
The SAOQ has 4 subscales and the score is determined by calculating the mean of certain items corresponding to each subscale.
Higher scores indicate greater frequency of experienced outcomes.
|
Baseline, Mid-intervention (6 weeks), and Post-intervention (12 weeks)
|
|
Mindfulness
Time Frame: Baseline, Mid-intervention (6 weeks), and Post-intervention (12 weeks)
|
Mindfulness will be measured using the Mindful Attention Awareness Scale (MAAS).
The MAAS is a 15-item instrument scored on a 6-point Likert scale (1- Almost Always, 2- Very Frequently, 3- Somewhat Frequently, 4- Somewhat Infrequently, 5- Very Infrequently, 6- Almost Never).
Higher scores indicate greater levels of mindfulness.
|
Baseline, Mid-intervention (6 weeks), and Post-intervention (12 weeks)
|
|
Subjective physical activity
Time Frame: Baseline, Mid-intervention (6 weeks), and Post-intervention (12 weeks)
|
Subjective physical activity will be measured using the Pregnancy Physical Activity Questionnaire (PPAQ).
The instrument assesses the approximate amount of time spent in 32 activities including household/caregiving, occupational, sports/exercise, and inactivity during the current trimester.
Duration and intensity will be determined using Compendium-based MET values.
|
Baseline, Mid-intervention (6 weeks), and Post-intervention (12 weeks)
|
|
Objective physical activity (steps)
Time Frame: Daily for 12 weeks
|
The number of steps per day will be measured using the Garmin Vivosmart 5 fitness tracker.
|
Daily for 12 weeks
|
|
Objective physical activity (intensity)
Time Frame: Daily for 12 weeks
|
Intensity of activity will be measured using metabolic equivalents (METs) value via the Garmin Vivosmart 5 fitness tracker.
|
Daily for 12 weeks
|
|
Cardiac health (heart rate)
Time Frame: Daily for 12 weeks
|
Heart rate in beats per minute (BPM) will be measured using the Garmin Vivosmart 5 fitness tracker.
|
Daily for 12 weeks
|
|
Cardiac health (heart rate variability)
Time Frame: Daily for 12 weeks
|
Heart rate variability in milliseconds will be measured using the Garmin Vivosmart 5 fitness tracker.
|
Daily for 12 weeks
|
|
Cultural adaptations
Time Frame: Post-Intervention (12 weeks)
|
Qualitative interviews will be used to explore and identify cultural adaptations relevant for African American pregnant women.
|
Post-Intervention (12 weeks)
|
|
Birth outcomes (gestational age)
Time Frame: Post-delivery (~2 weeks after delivery of baby)
|
Self-report survey will be used to assess gestational age (total length of pregnancy in weeks).
|
Post-delivery (~2 weeks after delivery of baby)
|
|
Birth outcomes (type of delivery)
Time Frame: Post-delivery (~2 weeks after delivery of baby)
|
Self-report survey will be used to assess the type of delivery (e.g., vaginal, planned C-section, unplanned C-section).
|
Post-delivery (~2 weeks after delivery of baby)
|
|
Birth outcomes (intervention used for delivery)
Time Frame: Post-delivery (~2 weeks after delivery of baby)
|
Self-report survey will be used to assess interventions used for delivery, if applicable, using a list.
An intervention can include use of medical treatments or procedures to induce labor or assist with delivery.
|
Post-delivery (~2 weeks after delivery of baby)
|
|
Birth outcomes (birth weight)
Time Frame: Post-delivery (~2 weeks after delivery of baby)
|
Self-report survey will be used to assess birth weight (weight of baby in pounds + ounces).
|
Post-delivery (~2 weeks after delivery of baby)
|
|
Birth outcomes (maternal weight)
Time Frame: Post-delivery (~2 weeks after delivery of baby)
|
Self-report survey will be used to assess maternal weight (last known weight before delivery in pounds).
|
Post-delivery (~2 weeks after delivery of baby)
|
|
Birth outcomes (pregnancy-related disorders)
Time Frame: Post-delivery (~2 weeks after delivery of baby)
|
Self-report survey will be used to assess pregnancy-related disorders, if applicable, using a list.
Pregnancy-related disorders could be complications including physical and mental conditions that affect the health of the pregnant or postpartum person, their baby, or both (e.g.,preterm birth, gestational diabetes, preeclampsia, eclampsia, birth injury, postpartum hemorrhage, postpartum hypertension etc.)
|
Post-delivery (~2 weeks after delivery of baby)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jeni Green, PhD, San Diego State University
Publications and helpful links
General Publications
- MacDorman MF, Thoma M, Declcerq E, Howell EA. Racial and Ethnic Disparities in Maternal Mortality in the United States Using Enhanced Vital Records, 2016-2017. Am J Public Health. 2021 Sep;111(9):1673-1681. doi: 10.2105/AJPH.2021.306375. Epub 2021 Aug 12.
- Ely DM, Driscoll AK. Infant Mortality in the United States, 2020: Data From the Period Linked Birth/Infant Death File. Natl Vital Stat Rep. 2022 Sep;71(5):1-18.
- Giurgescu C, Kavanaugh K, Norr KF, Dancy BL, Twigg N, McFarlin BL, Engeland CG, Hennessy MD, White-Traut RC. Stressors, resources, and stress responses in pregnant African American women: a mixed-methods pilot study. J Perinat Neonatal Nurs. 2013 Jan-Mar;27(1):81-96. doi: 10.1097/JPN.0b013e31828363c3.
- Knuist M, Bonsel GJ, Zondervan HA, Treffers PE. Risk factors for preeclampsia in nulliparous women in distinct ethnic groups: a prospective cohort study. Obstet Gynecol. 1998 Aug;92(2):174-8. doi: 10.1016/s0029-7844(98)00143-4.
- Brown HL, Chireau MV, Jallah Y, Howard D. The "Hispanic paradox": an investigation of racial disparity in pregnancy outcomes at a tertiary care medical center. Am J Obstet Gynecol. 2007 Aug;197(2):197.e1-7; discussion 197.e7-9. doi: 10.1016/j.ajog.2007.04.036.
- Dagher RK, Linares DE. A Critical Review on the Complex Interplay between Social Determinants of Health and Maternal and Infant Mortality. Children (Basel). 2022 Mar 10;9(3):394. doi: 10.3390/children9030394.
- Larson CP. Poverty during pregnancy: Its effects on child health outcomes. Paediatr Child Health. 2007 Oct;12(8):673-7. doi: 10.1093/pch/12.8.673.
- Narendran S, Nagarathna R, Narendran V, Gunasheela S, Nagendra HR. Efficacy of yoga on pregnancy outcome. J Altern Complement Med. 2005 Apr;11(2):237-44. doi: 10.1089/acm.2005.11.237.
- Green J, James D, Larkey L, Leiferman J, Buman M, Oh C, Huberty J. A qualitative investigation of a prenatal yoga intervention to prevent excessive gestational weight gain: A thematic analysis of interviews. Complement Ther Clin Pract. 2021 Aug;44:101414. doi: 10.1016/j.ctcp.2021.101414. Epub 2021 May 6.
- Battle CL, Uebelacker LA, Magee SR, Sutton KA, Miller IW. Potential for prenatal yoga to serve as an intervention to treat depression during pregnancy. Womens Health Issues. 2015 Mar-Apr;25(2):134-41. doi: 10.1016/j.whi.2014.12.003.
- Green J, Neher T, Puzia M, Laird B, Huberty J. Pregnant women's use of a consumer-based meditation mobile app: A descriptive study. Digit Health. 2022 Mar 27;8:20552076221089098. doi: 10.1177/20552076221089098. eCollection 2022 Jan-Dec.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HS-2023-0254
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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