- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05131360
Reducing Daily Stress Among Sexual and Gender Minorities (REDUCE)
Reducing Daily Stress Among Sexual and Gender Minorities (the REDUCE Study)
Study Overview
Status
Detailed Description
Underrepresented racial/ethnic sexual and gender minorities (SGM) aged 18-29 will be recruited via convenience sampling from social media websites (e.g. Facebook, Instagram) and listservs from NYU student groups and through LGBT community partners. Interested persons who screen eligible through the study's online eligibility screener will be asked to provide their phone number and/or email address to be contacted by a research assistant. An online meeting via Zoom will then be scheduled to confirm eligibility, provide additional information concerning study parameters. The online meeting will be between the research assistant and a single participant. The meeting will take between 10 to 15 minutes depending on the questions individuals may have. The meeting will be an informational assessment to assure that the individual can effectively use and have access to the materials used in the study, the online surveys/assessments, and interventions.
After providing online informed consent through REDCap, the participant will be randomized into one of the 8 mindfulness conditions, complete a 30-minute baseline survey via REDCap, and be provided with training on study protocols. Participants will engage in the study of a 5-day period (starting after the baseline survey). Participants will engage in one of 8 interventions, depending on randomization, in which participants will engage with mindfulness activities each night for a total of 5 nights which is expected to take 10-20 minutes per day (the exception to this is the control condition who only receives an introduction to mindfulness on day 1). In addition, each night over the 5-day period, participants will be sent a REDCap survey to complete a "nightly diary" which will take about 5 minutes to complete.
After completion of the 5-day protocol, participants will be scheduled for an online Zoom meeting where participants will engage in a 30-40 minute debrief interview and be renumerated. The Zoom meetings will be between a research assistant and a single participant. Lastly, in order to improve retention, RA's will perform check-in calls twice during the 5-day daily diary period.
The interventions will be administered using the multiphase optimization strategy (MOST). The participants will be randomized to at least one of the 3 intervention components of Awareness, Purpose, and Connection for this optimization study, which make up the 8 conditions. Each of these components is known to be effective in reducing stress and promoting well-being among populations that experience a high rate of discrimination (e.g., SGM). The three components are administered via the Healthy Minds Program (HMP), which is a smartphone app-based mindfulness intervention developed through the research of Dr. Richard Davidson and his team at the University of Wisconsin-Madison's Center for Healthy Minds in affiliation with the non-profit Healthy Minds Innovations (HMI). The app provides an average of 10-minute meditations that can be completed while sitting, walking, or exercising that focus on the modules of Awareness, Purpose, and Connection. Participants will log into the app and listen to the meditations that correspond to their selected randomization on each of the 5 days. The app's methodology aligns with constituents of psychological well-being that are trainable and measurable as evidenced by the Center for Healthy Minds: Awareness, Purpose, and Connection. The components are as follows: 1) Awareness through meditation promotes self-awareness, reducing the mind's ability to be distracted and instead be present at the moment. Awareness promotes well-being by bringing attention to the present moment, not allowing the mind to wander to negative thoughts that cause stress; 2) Purpose through meditation promotes mindfulness of one's thoughts and feelings in the present moment and encourages compassion with oneself and positive reappraisal; 3) Connection through meditation supports empathy, compassion, and kindness in daily activities. By shifting to this positive mindset, individuals are able to cultivate social support networks which research has found to decrease the risk for depression.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Stephanie H Cook, DrPH
- Phone Number: 212-992-5635
- Email: sc5810@nyu.edu
Study Contact Backup
- Name: Erica P Wood, MPH
- Phone Number: 832-776-1095
- Email: ew71@nyu.edu
Study Locations
-
-
New York
-
New York, New York, United States, 10003
- Recruiting
- New York University School of Global Public Health
-
Contact:
- Stephanie H Cook, DrPH
- Phone Number: 212-992-5635
- Email: sc5810@nyu.edu
-
Contact:
- Erica P Wood, MPH
- Phone Number: 832-776-1095
- Email: ew71@nyu.edu
-
Principal Investigator:
- Stephanie H Cook, DrPH
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Between 18-29 years
- Must identify as a sexual minority (e.g. gay, bisexual, sexually fluid, etc.)
- Must identify as an underrepresented racial/ethnic minority
- Have an active cell phone service and be able to access the cell phone 7 days a week between 6 p.m. and 6 a.m. the next morning
- Be willing and able to receive up to 6 text messages per day
- Have consistent Internet access 7 days a week between 6 p.m. and 6 a.m.
- Can understand, read, and speak English
- Willing to provide written informed consent.
Exclusion Criteria:
- Not between 18-29 years
- Does not identify as a sexual minority (e.g. gay, bisexual, sexually fluid, etc.)
- Does not identify as an underrepresented racial/ethnic minority
- Does not have an active cell phone service and or ability to access the cell phone 7 days a week between 6 p.m. and 6 a.m. the next morning
- Not willing and able to receive up to 6 text messages per day
- Does not have consistent Internet access 7 days a week between 6 p.m. and 6 a.m.
- Does not have the ability to understand, read, and speak English
- Not willing to provide written informed consent.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: Introduction Only
This is the control; participants only partake in one day's worth of the introduction or foundational mindfulness activities on the HMI app.
|
This is the placebo condition in which participants engage in one day of introductory mindfulness activities.
|
|
Experimental: Purpose Only
Participants partake in the introduction or foundational mindfulness for one day and then perform purpose-based mindfulness techniques for 5 days on the HMI app.
|
Participants engage in one day of introductory mindfulness activities followed up by 5 days of purpose-based mindfulness techniques.
|
|
Experimental: Connection Only
Participants partake in the introduction or foundational mindfulness for one day and then perform connection-based mindfulness techniques for 5 days on the HMI app.
|
Participants engage in one day of introductory mindfulness activities followed up by 5 days of connection-based mindfulness techniques.
|
|
Experimental: Connection and Purpose
Participants partake in the introduction or foundational mindfulness for one day and then perform connection and purpose-based mindfulness techniques for 5 days on the HMI app.
|
Participants engage in one day of introductory mindfulness activities followed up by 5 days of connection and purpose-based mindfulness techniques.
|
|
Experimental: Awareness Only
Participants partake in the introduction or foundational mindfulness for one day and then perform awareness-based mindfulness techniques for 5 days on the HMI app.
|
Participants engage in one day of introductory mindfulness activities followed up by 5 days of awareness-based mindfulness techniques.
|
|
Experimental: Awareness and Purpose
Participants partake in the introduction or foundational mindfulness for one day and then perform awareness and connection-based mindfulness techniques for 5 days on the HMI app.
|
Participants engage in one day of introductory mindfulness activities followed up by 5 days of awareness and purpose-based mindfulness techniques.
|
|
Experimental: Awareness, Purpose, and Connection
Participants partake in the introduction or foundational mindfulness for one day and then perform connection, awareness, and purpose-based mindfulness techniques for 5 days on the HMI app.
|
Participants engage in one day of introductory mindfulness activities followed up by 5 days of awareness, connection, and purpose-based mindfulness techniques
|
|
Experimental: Awareness and Connection
Participants partake in the introduction or foundational mindfulness for one day and then perform awareness and connection-based mindfulness techniques for 5 days on the HMI app.
|
Participants engage in one day of introductory mindfulness activities followed up by 5 days of awareness and connection-based mindfulness techniques.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline in Perceived Stress on the Perceived Stress Scale at Day 5
Time Frame: Baseline through study completion, up to one year
|
The primary outcome for this study is change in perceived stress as measured by the Perceived Stress Scale from baseline to Day 5 among all study participants.
|
Baseline through study completion, up to one year
|
|
Change from Baseline in Satisfaction with Life on the Satisfaction with Life Scale at Day 5
Time Frame: Baseline through study completion, up to one year
|
The primary outcome for this study is change in perceived satisfaction with life as measured by the Satisfaction with Life Scale from baseline to Day 5 among all study participants.
|
Baseline through study completion, up to one year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Optimized Intervention Package
Time Frame: Through study completion, an average of 1 year
|
An optimal intervention combination will be determined with the primary outcomes of perceived stress (as measured through the Perceived Stress Scale) and satisfaction with life (as measured through the Satisfaction with Life Scale) by looking at changes in mean perceived stress and satisfaction with life across all intervention categories.
|
Through study completion, an average of 1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Stephanie H Cook, DrPH, New York University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- IRB-FY2020-4338
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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