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Mindfulness Intervention Group for Anxiety

N/A
Waitlist Available
Led By Christopher M Morosky, MD
Research Sponsored by UConn Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up over the course of 6 intervention sessions, followed by 6 weeks postpartum
Awards & highlights

Study Summary

This study is evaluating whether a mindfulness audio clip can lower levels of anxiety and depression in pregnant women.

Eligible Conditions
  • Anxiety
  • Mindfulness
  • Depression

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~over the course of 6 intervention sessions, followed by 6 weeks postpartum
This trial's timeline: 3 weeks for screening, Varies for treatment, and over the course of 6 intervention sessions, followed by 6 weeks postpartum for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Beck Anxiety Inventory Score
Edinburgh Postnatal Depression Scale Score

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Mindfulness Intervention GroupExperimental Treatment1 Intervention
Participants in this group will listen to a short mindfulness audio clip during 6 of their NST appointments.
Group II: Control GroupActive Control1 Intervention
Participants in this group will have the regular standard of care for their NST appointments.

Find a Location

Who is running the clinical trial?

UConn HealthLead Sponsor
211 Previous Clinical Trials
60,541 Total Patients Enrolled
2 Trials studying Anxiety
114 Patients Enrolled for Anxiety
Christopher M Morosky, MDPrincipal InvestigatorUConn Health

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~12 spots leftby Apr 2025