← Back to Search

Stress Reduction Programs for Emotional Well-being

N/A
Waitlist Available
Research Sponsored by Virginia Commonwealth University
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 baseline to post intervention, approximately 2 weeks
Awards & highlights

Study Summary

This trial investigates the effects of online stress reduction programs on people's everyday experiences and relationships. Researchers hope to learn how these programs can improve mental health.

Who is the study for?
This trial is for Virginia Commonwealth University students who are at least 18 years old, healthy, fluent in English, non-immigrants, not currently practicing stress reduction for over an hour a week, and own a smartphone. It's not open to those with psychiatric conditions or histories, recent medical diagnoses, drug abuse issues, or major sensory and cognitive impairments.Check my eligibility
What is being tested?
The study compares two online stress reduction programs to see how they affect participants' daily emotions and social interactions. The goal is to determine the impact of these programs on real-world psychological outcomes.See study design
What are the potential side effects?
Since this trial involves non-medical interventions like stress reduction training via smartphones, significant side effects are not anticipated. However, participants may experience changes in mood or behavior as they engage with the program.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to post intervention, approximately 2 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline to post intervention, approximately 2 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in state emotion regulation

Trial Design

3Treatment groups
Experimental Treatment
Active Control
Group I: Stress reduction program 2Experimental Treatment1 Intervention
Participants will complete stress reduction lessons for two weeks
Group II: Stress reduction program 1Experimental Treatment1 Intervention
Participants will complete stress reduction lessons for two weeks
Group III: WaitlistActive Control1 Intervention
Participants will have an opportunity to complete one of the two programs of stress reduction lessons after data collection is completed
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Stress reduction program 1
2023
N/A
~130
Stress reduction program 2
2023
N/A
~130

Find a Location

Who is running the clinical trial?

Virginia Commonwealth UniversityLead Sponsor
700 Previous Clinical Trials
22,886,695 Total Patients Enrolled

Media Library

Stress reduction program 1 Clinical Trial Eligibility Overview. Trial Name: NCT05730270 — N/A
Emotions Research Study Groups: Stress reduction program 1, Stress reduction program 2, Waitlist
Emotions Clinical Trial 2023: Stress reduction program 1 Highlights & Side Effects. Trial Name: NCT05730270 — N/A
Stress reduction program 1 2023 Treatment Timeline for Medical Study. Trial Name: NCT05730270 — N/A
~58 spots leftby Jun 2025
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Back to top