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Finding Emotional Empowerment and Lifelong Strength

Co-Producing a Trauma and Substance Use Mental Health Literacy Intervention

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07378254
Acronym
FEELS
Enrollment
80
Registered
2026-01-30
Start date
2026-03-10
Completion date
2028-06-01
Last updated
2026-06-18

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

Conditions

Substance Use, Trauma and Stressor Related Disorders

Keywords

mental health literacy, trauma, substance use, psychoeducation, Black and African American, young adults

Brief summary

This study will build a partnership with a Community Advisory Board to co-produce, and then pilot test, a theory-guided mental health literacy intervention focused on trauma and substance use. Participants will take part in educational group sessions for 12 weeks and complete assessments at baseline and two follow-up time points (mid-intervention and post-intervention). Intervention participants will be randomly invited to post-study focus groups to gather feedback on their experiences in the program.

Detailed description

This study will enhance mental health literacy (i.e., knowledge and beliefs related to mental health, including recognition, prevention, and management of symptoms) among a sample of young Black adults who have experienced lifetime trauma. The culturally tailored intervention will be guided by the Theory of Planned Behavior and social ecological model as guiding frameworks. Intervention components will be designed to promote behavioral, normative, and control beliefs related to mental health care utilization, with resources to target individual, interpersonal, organizational, and community levels of influence. Following development, the intervention will be piloted among young Black adults, utilizing a single-arm pilot design.

Interventions

BEHAVIORALFinding Emotional Empowerment and Lifelong Strength

A group-based, 12-week educational intervention to help promote mental health literacy and related beliefs, especially related to trauma and substance use.

Sponsors

Rutgers, The State University of New Jersey
Lead SponsorOTHER
National Institute of Mental Health (NIMH)
CollaboratorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

1. Self-identify as Black or African American 2. Be between the ages of 18 and 35 years old 3. Endorse previous lifetime trauma exposure 4. Participants must speak English 5. Participants are capable of giving informed consent and capable of complying with study procedures.

Design outcomes

Primary

MeasureTime frameDescription
Change in scores on the Multicomponent Mental Health Literacy Measure (MMHLM)3-monthsAssesses knowledge and beliefs about mental health disorders, including symptoms, causes, prevention and treatment strategies. Total scores range from 22 to 110, with higher scores indicating greater MHL.
Change in scores on the Short Attitudes Towards Mental Health Problems Scale (SATMHPS)3-monthsMeasures personal, family, and community attitudes and stigma related to mental health challenges. Mean scores for subscales range from 0 to 3, with higher scores indicating more negative attitudes.
Change in scores on the Mental Help Seeking Intention Scale (MHSIS)3-monthsMeasures intentions to seek help from a mental health professional in the event of a mental health concern. Mean scores range from from 1 to 7, with higher scores indicating stronger intentions.
Change in scores on the Self-Efficacy in Seeking Mental Health Care (SE-SMHC)3-monthsAssesses perceived ability to seek professional mental health care. Total scores range from 9 to 90, while subscale scores range from 5 to 50 (SE-KNOW) and 4 to 40 (SE-COPE).
Participant engagement as assessed by rates of participant recruitment and proportion of eligible participants who are enrolled in the study3-months
Participant satisfaction at mid- and post-intervention (quantitative)3-monthsMean scores (ranging from 1 to 5) on ten Likert items assessing length of the program, pace of learning and discussing material, group format, meeting time and location, group facilitator, and program materials (i.e., amount of information given, clarity of the information given, ability to understand information, ability to apply material in real life). One additional item will ask how participants would rate the helpfulness of the FEELS intervention (1 = very unhelpful to 5 = very helpful).
Participant satisfaction at post-intervention (qualitative)3-monthsThree survey questions will ask participants for feedback on the intervention (facilitators for participation, topics to include in the future, and suggestions for improvement). Post-intervention focus groups will also elicit qualitative appraisals (on intervention length, pace, and modality; ease of reading, understanding, and applying the content; and suggestions for improvement) from a smaller group of intervention participants.
Participant retention and attendance at sessions3-monthsMean number of intervention sessions attended per participant and proportion of participants who complete the full intervention

Secondary

MeasureTime frameDescription
Mental health help-seeking behaviors3-monthsFive questions will include looking for a mental health provider nearby, finding out whether insurance would cover a visit to a mental health provider, making an appointment, following through on the appointment, and/or visiting a provider more than once. Items will be scored as 1 = Yes and 0 = No.
Changes in scores on the Short PTSD Rating Interview (SPRINT)3-monthsMean scores ranging from 0 to 4, with higher scores indicating greater PTSD symptoms.
Changes in scores on the Alcohol, Smoking, and Substance Involvement Screening Test (ASSIST)3-monthsMean frequency of past 3-month substance use, ranging from 0 to 6, with higher scores indicating greater substance use.

Countries

United States

Contacts

CONTACTAlexandria Bauer, PhD
alexandria.bauer@rutgers.edu848-209-1032

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 19, 2026