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Clinical Trial Details — Status: Suspended

Administrative data

NCT number NCT05087329
Other study ID # 843962
Secondary ID
Status Suspended
Phase N/A
First received
Last updated
Start date May 5, 2021
Est. completion date December 2024

Study information

Verified date February 2024
Source University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to examine whether a simple mindfulness intervention conducted via a virtual platform can reduce stress among pregnant women.


Recruitment information / eligibility

Status Suspended
Enrollment 248
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Women between 16w0d-26w6d gestation with a single gestation who have had a confirmed dating ultrasound a. Only women with singleton gestations will be included because multiple gestation pregnancies introduce additional levels of stress and introduce confounding variables for the adverse composite pregnancy outcome that will be measured. As this is a study of pregnant patients, only women are included. 2. English speaking a. The mindfulness meditation trainings have been scripted and recorded in English. Thus, to understand the recordings and participate in the courses it is necessary for all participants to speak English. 3. Regular internet access through either phone, tablet or computer. a. Mindfulness meditations are administered via Zoom webinars so internet access is required. A proxy for internet access during recruitment will be confirmed by the inclusion of an email address in the electronic medical record (EMR). Exclusion Criteria: 1. Multiple gestations. This has been chosen as an exclusion criteria to limit confounding variables for the secondary outcome of composite adverse pregnancy events. 2. Age < 18

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Virtual Mindfulness Meditation
Four week virtual mindfulness meditation course composed of four weekly group Zoom webinars during which participants will listen to a 15-20 minute pre-recorded meditation, facilitated by a study provider

Locations

Country Name City State
United States University of Pennsylvania Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Decrease in Maternal Stress Change in score on Perceived Stress Scale (PSS) 6 to 8 weeks
Secondary Composite score of maternal morbidity/pregnancy outcomes 6 to 8 weeks post-delivery
Secondary Change in score on Edinburgh Postnatal Depression Scale change between score at time of delivery and 6 weeks
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