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Reducing Daily Stress Among Sexual and Gender Minorities

Reducing Daily Stress Among Sexual and Gender Minorities (the REDUCE Study)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05131360
Acronym
REDUCE
Enrollment
80
Registered
2021-11-23
Start date
2021-01-01
Completion date
2022-03-30
Last updated
2021-11-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mindfulness, Sexual and Gender Minorities, Social Discrimination

Keywords

Social stress, Stress from discrimination, Mindfulness, Anxiety, Depression, Sexual and gender minorities

Brief summary

The purpose of this study is to identify which mindfulness technique, or combination of mindfulness techniques, is most effective at mediating or eliminating stress in emerging adults who are sexual and gender as well as racial or ethnic minorities. Participants will be randomly assigned to one of eight conditions that are composed of the mindfulness techniques of Awareness, Purpose, and Connection.

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.

Interventions

BEHAVIORALIntroduction Only

This is the placebo condition in which participants engage in one day of introductory mindfulness activities.

BEHAVIORALPurpose Only

Participants engage in one day of introductory mindfulness activities followed up by 5 days of purpose-based mindfulness techniques.

BEHAVIORALConnection Only

Participants engage in one day of introductory mindfulness activities followed up by 5 days of connection-based mindfulness techniques.

BEHAVIORALConnection and Purpose

Participants engage in one day of introductory mindfulness activities followed up by 5 days of connection and purpose-based mindfulness techniques.

BEHAVIORALAwareness Only

Participants engage in one day of introductory mindfulness activities followed up by 5 days of awareness-based mindfulness techniques.

BEHAVIORALAwareness and Purpose

Participants engage in one day of introductory mindfulness activities followed up by 5 days of awareness and purpose-based mindfulness techniques.

BEHAVIORALAwareness, Purpose, and Connection

Participants engage in one day of introductory mindfulness activities followed up by 5 days of awareness, connection, and purpose-based mindfulness techniques

BEHAVIORALAwareness and Connection

Participants engage in one day of introductory mindfulness activities followed up by 5 days of awareness and connection-based mindfulness techniques.

Sponsors

New York University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 29 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in Perceived Stress on the Perceived Stress Scale at Day 5Baseline through study completion, up to one yearThe 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.
Change from Baseline in Satisfaction with Life on the Satisfaction with Life Scale at Day 5Baseline through study completion, up to one yearThe 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.

Secondary

MeasureTime frameDescription
Optimized Intervention PackageThrough study completion, an average of 1 yearAn 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.

Countries

United States

Contacts

Primary ContactStephanie H Cook, DrPH
sc5810@nyu.edu212-992-5635
Backup ContactErica P Wood, MPH
ew71@nyu.edu832-776-1095

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026