Paid Anxiety and Postpartum Anxiety Research Study
Researchers at the University of Pennsylvania are conducting a study with individuals who are pregnant or postpartum to learn more about mood and anxiety during the perinatal period.
Fast Facts
Currently 14+ Weeks Pregnant OR up to 9 Months Postpartum
Diagnosed with or Experiencing Symptoms of Anxiety
Compensation Provided
Conducted in
Philadelphia, PA
Study Background
Help researchers identify important triggers of perinatal anxiety and find the best time to intervene.
We want to find modern solutions to identify and treat individuals who are at risk for anxiety during the perinatal period. The purpose of this study is to investigate how anxiety develops and is maintained in both pregnant and postpartum individuals.
To help us better understand these fluctuations in anxiety, participants will answer daily questionnaires about mood, anxiety, sleep, infant concerns, and suicidal urges. Participants will also be provided a Fitbit, which will track sleep and activity levels for the duration of the study.
Study Background
Help researchers identify important triggers of perinatal anxiety and find the best time to intervene.
We want to find modern solutions to identify and treat individuals who are at risk for anxiety during the perinatal period. The purpose of this study is to investigate how anxiety develops and is maintained in both pregnant and postpartum individuals.
To help us better understand these fluctuations in anxiety, participants will answer daily questionnaires about mood, anxiety, sleep, infant concerns, and suicidal urges. Participants will also be provided a Fitbit, which will track sleep and activity levels for the duration of the study.
Additional Information
The purpose of this research study is to identify important triggers of perinatal anxiety and find the best time to intervene.
You may qualify for a study if you meet the following criteria.
Inclusion Criteria:
- Ages 18+
- Currently 14+ weeks pregnant OR up to 9 months postpartum
- Diagnosed with an anxiety disorder or experiencing symptoms of anxiety
- Able to wear a Fitbit
After a brief phone screen and in-person baseline assessment, the 28-day study will begin.
During this time, participants will receive 4 text message prompts per day to complete questionnaires about mood, anxiety, sleep, infant concerns, and suicidal urges. Participants will also be provided a Fitbit, which will be used to track sleep and activity levels for the duration of the study.
The second and final in-person visit will take place at the end of the 28 days and will consist of self-report measures and an exit interview. Participants will also be asked to return the Fitbit during this final visit.
As a participant, you can receive up to $232 in Greenphire ClinCards for completing all study visits. Greenphire ClinCards can be used like any debit card.
Additionally, participants can be reimbursed for travel costs up to $20 per visit
There is no cost for you to participate in our research study.
