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Improving Physical, Mental, and Spiritual Health in Faith-Based Settings Through Creating a Healthy Culture in Bronx, NY

Improving Physical, Mental, and Spiritual Health in Faith-Based Settings Through Creating a Healthy Culture in Bronx, NY

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04353427
Enrollment
108
Registered
2020-04-20
Start date
2020-05-01
Completion date
2021-02-01
Last updated
2021-03-18

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

Conditions

Mental Health Issue

Brief summary

The proposed study Improving Physical, Mental, and Spiritual Health in Faith- Based Settings through Creating a Healthy Culture in Bronx, NY aims to assess the efficacy of a holistic health intervention that seeks to integrate physical, mental, spiritual, and community engagement processes into faith-based settings, compared to usual care in Bronx, NY. Briefly, the intervention involves a seven-session faith-based small group education program conducted by trained lay educators. A health ministry at each partner religious institution will be developed and sustained

Detailed description

The purpose of this research study is test a holistic health intervention that combines physical, mental, spiritual, and community processes into faith-based settings in Bronx, NY. The program involves a seven-session faith-based small group education sessions to be conducted by lay educators.

Interventions

BEHAVIORALThe Seven Pathways to Healing, Health and Wellness curriculum

The curriculum seeks to increase civic engagement by fostering a sense of community and a sense of social and personal responsibility in community. There will be 7 monthly session that will be approximately 1 hour in duration. Session topics include: 1. Education and Information (including mental health awareness, and a one-day certificate program in Mental Health First Aid) 2. Connection with Others 3. The Body as Temple 4. Emotional Healing 5. The Nature of Mind 6. Life Assessment 7. The Nature of Spirit

Sponsors

NYU Langone Health
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

Intervention study participants Inclusion Criteria: * Age 18 and over * Self-identify as a member of the religious institution for at least three months * Able to read and speak in English, Vietnamese, or Khmer

Exclusion criteria

* Any serious health issue that may interfere with the study procedures Key informants participants Inclusion Criteria: * Age 18 and over * Must be a study implementation partner, a health ministry member, or lay educator

Design outcomes

Primary

MeasureTime frameDescription
Changes in sociodemographic characteristics of participantsbaseline and 6 months visitThis will be measured by self reported participant survey about the aspects of personal and social responsibility for well-being.

Secondary

MeasureTime frameDescription
Facilitators and Barriers in intervention process by Focus Group participants6 monthsA Focus group of a subset of participants will assess the facilitators and barriers in receiving the 7 sessions of the intervention. The focus groups at a private location convenient for participants. Interviews will not exceed two hours and will be audio-recorded. The focus group data will elicit facilitators and barriers to receiving the intervention and making change to improve well-being. The focus group will discuss topics such as how the group sessions impacted on the participants' physical or mental health, what was challenging or not useful and what types of tools were gained that were helpful to become more spiritually healthy.
Facilitators and Barriers in intervention process by Key informants6 monthsThe key informant interviews will contain questions that assess facilitators and barriers to implementing the intervention. The key informant interviews will be conducted once, immediately after completion of the intervention among intervention participants

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026