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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05730270
Other study ID # HM20021623
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date March 30, 2023
Est. completion date May 2024

Study information

Verified date May 2023
Source Virginia Commonwealth University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this research study is to find out how two different online stress reduction training programs affect people's daily experiences and social relations. The researchers think that people's thoughts, emotions, and behavior toward others may be influenced by stress reduction programs. This study will allow them to study the effectiveness of stress reduction programs for important real-world psychological outcomes.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 100
Est. completion date May 2024
Est. primary completion date May 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Virginia Commonwealth University students - age 18 years or older - Healthy - English literate - non-immigrant - not practicing stress reduction techniques for more than 60 minutes a week - ownership of a smartphone Exclusion Criteria: - People who are not Virginia Commonwealth University students - major, uncorrected sensory impairments and cognitive deficits - psychiatric disorders or history thereof - new diagnosis of a (non-acute) medical or psychiatric condition within the last 3 months - current drug abuse

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Stress reduction program 1
Participants will receive daily online lessons
Stress reduction program 2
Participants will receive daily online lessons

Locations

Country Name City State
United States Virginia Commonwealth University Richmond Virginia

Sponsors (1)

Lead Sponsor Collaborator
Virginia Commonwealth University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in state emotion regulation Participants will complete a state emotion strategies measure which will ask them to check various actions they are taking to change their thoughts and feelings. Change in total number of actions checked will be calculated. Baseline to post intervention, approximately 2 weeks
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