Sexual and Gender Minority Emerging Adults Eliciting Narratives
SEEN
1 other identifier
interventional
20
1 country
1
Brief Summary
Critical narrative interventions (CNIs) have not been examined for addressing psychological outcomes (e.g., depression, anxiety, self-esteem, empowerment, psychological well-being) within sexual and gender minority emerging adults (SGM EA) of color; therefore, this pilot study will examine the use of CNIs to impact SGM of color psychological outcomes. Prior literature has shown that CNIs have the potential to increase empowerment, self-efficacy, and social support as a prevention strategy for mental health. The research study is being conducted to see if telling your story through photographs or video can improve the mental health and well-being of emerging adults that identify as a member of a sexual and/or gender minority and a racial and/or ethnic minority. Participants will be asked to complete the following research procedures:
- 1.take a survey online (about 20-30 minutes), then an interview about everyday experiences as sexual/gender minority of color and your experiences in seeking out mental health services.
- 2.After the interview, participants will have one month to tell their story, answering two prompts "Tell us a time you have felt seen" and "Tell us a time when you have felt unseen." You will be randomized to one of two formats of telling your story: taking photographs or making two short videos.
- 3.Photographs: Those that are randomized to the photograph condition will be asked to take 12 photos total telling your story and answering the prompt.
- 4.Videos: Those that are randomized to the video condition will be asked to create two (1-3 minute) videos telling your story and answering the prompts.
- 5.At the one-month time frame, participants will be asked to fill out another survey (about 20-30 minutes) and then complete an interview about the photos or videos created.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jul 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 19, 2023
CompletedFirst Posted
Study publicly available on registry
June 12, 2023
CompletedStudy Start
First participant enrolled
July 17, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2024
CompletedResults Posted
Study results publicly available
November 25, 2024
CompletedNovember 25, 2024
October 1, 2024
9 months
May 19, 2023
June 28, 2024
October 4, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Patient Health Questionnaire (PHQ-9)
scores range from 0 to 27, higher scores indicate higher levels of depression severity.
1 month
Generalized Anxiety Disorder-7 (GAD-7)
scores range from 0 to 21, higher scores indicate higher levels of anxiety severity.
1 month
The Flourishing Scale
scores range from 8 to 56, higher scores represent an individual with many psychological resources and strengths.
1 month
Rosenberg Self-Esteem Scale
scores range from 8 to 56, higher scores represent an individual with higher self-esteem.
1 month
Secondary Outcomes (7)
Internalized Stigma of Mental Illness Scale (ISMI-9)
1 month
LGBTQ+ POC Microaggressions Scale-Brief (LGBTQ+ PCMS-B): Racism in Dating Subscale
1 month
Attitudes Toward Mental Health Treatment (ATMHT) Scale
1 month
General Belongingness Scale (GBS): Sense of Acceptance Sub Scale
1 month
Multidimensional Scale of Perceived Social Support (MSPSS)
1 month
- +2 more secondary outcomes
Other Outcomes (3)
Acceptability of the Intervention Measure (AIM)
1 month
Intervention Appropriateness of the Measure (IAM)
1 month
Feasibility of the Intervention Measure (FIM)
1 month
Study Arms (2)
Photo-Novella
EXPERIMENTALParticipants in the photo-novella intervention will be asked to take 12 photographs and write a caption for each photo based on two prompts.
Digital Storytelling
EXPERIMENTALParticipants in the digital storytelling intervention will be asked to create two videos (1-3 minutes each) based on two prompts.
Interventions
Participants are asked to answer two prompts ("describe an experience where you have felt seen as an LGBTQ+ person of color" and "describe an experience where you have felt unseen as an LGBTQ+ person of color").
Eligibility Criteria
You may qualify if:
- identify as a sexual minority
- live in the United States
- identify as a person of color
- be aged 18-24 years
- have a smartphone and or computer access
- identify as living with moderate to severe depression as indicated on the PHQ-9 (score of 10 or higher)
- do not report suicidal ideation in the past month.
You may not qualify if:
- Identifies as a cisgender heterosexual man or woman
- Does not live in the United States
- Identifies as non-Hispanic white or Caucasian
- Is not between the ages of 18-24 years (inclusive)
- Does not have access to a smartphone or computer
- Plan to move out of the region for the next six months
- Does not consent to study procedures
- Meets criteria for an unmanaged psychotic disorder
- meets criteria for none to mild depression on the PHQ-9 (score of 9 or less)
- reports suicidal ideation in the past month
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
School of Nursing, University of Pennsylvania
Philadelphia, Pennsylvania, 19104, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Dr. Jennifer Tran
- Organization
- University of Pennsylvania
Study Officials
- PRINCIPAL INVESTIGATOR
Jennifer Tran, PhD
University of Pennsylvania
Publication Agreements
- PI is Sponsor Employee
- No
- Restrictive Agreement
- No
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 19, 2023
First Posted
June 12, 2023
Study Start
July 17, 2023
Primary Completion
April 1, 2024
Study Completion
April 1, 2024
Last Updated
November 25, 2024
Results First Posted
November 25, 2024
Record last verified: 2024-10
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
- Time Frame
- The data will be available 1 year after the completion of study. The data will be available indefiitely.
- Access Criteria
- Data is available for the community, academic researchers, and educational purposes.
After the completion of the study, we plan to share with other researchers the de-identified individual participant data (IPD). This will only include the quantitative survey data collected and baseline and follow-up.