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Virtual Mindfulness-Based Stress Reduction (MBSR) program for Quality of Life

N/A
Waitlist Available
Led By Mehrnoosh Faghih, MD
Research Sponsored by One Fertility
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
-Primary infertility and no prior fertility treatment
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights

Summary

This trial will compare a standard fertility treatment group to one with an 8-week virtual Mindfulness-Based Stress Reduction program to study fertility rates & mental health.

Eligible Conditions
  • Quality of Life
  • Infertility
  • Mental Health Issue

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Virtual Mindfulness-Based Stress Reduction (MBSR) programExperimental Treatment1 Intervention
Group II: ControlActive Control1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Mindfulness-Based Stress Reduction course
2010
N/A
~90

Find a Location

Who is running the clinical trial?

One FertilityLead Sponsor
3 Previous Clinical Trials
570 Total Patients Enrolled
Mehrnoosh Faghih, MDPrincipal InvestigatorMcMaster University, ONE Fertility

Media Library

Mindfulness-Based Stress Reduction course Clinical Trial Eligibility Overview. Trial Name: NCT05903638 — N/A
Quality of Life Research Study Groups: Virtual Mindfulness-Based Stress Reduction (MBSR) program, Control
Quality of Life Clinical Trial 2023: Mindfulness-Based Stress Reduction course Highlights & Side Effects. Trial Name: NCT05903638 — N/A
Mindfulness-Based Stress Reduction course 2023 Treatment Timeline for Medical Study. Trial Name: NCT05903638 — N/A
~8 spots leftby Sep 2025
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