Up To Me: Erasing the Stigma of Mental Illness on College Campuses

Sponsor
University of South Florida (Other)
Overall Status
Recruiting
CT.gov ID
NCT05784818
Collaborator
National Institute on Disability, Independent Living, and Rehabilitation Research (U.S. Fed), Temple University (Other), Illinois Institute of Technology (Other)
201
1
3
24.8
8.1

Study Details

Study Description

Brief Summary

This is a three-lesson, disclosure-based stigma reduction program meant to reduce barriers to community living and participation for college students with psychiatric disabilities. The goal is to improve community living and participation of individuals with psychiatric disabilities within their postsecondary community using the Honest Open Proud (HOP) program. There are 3 specific objectives of the project:1) evaluate program fidelity, 2) assess program feasibility, and 3) conduct a randomized controlled trial of the HOP program with college students with mental illness to examine its efficacy. Anticipated outcomes include increases in 1) community integration, 2)self-esteem and self-efficacy, 3) empowerment and self-determination, 4) disclosure of mental illness in order to obtain needed support, and 5) care seeking/service engagement for mental illness. Ultimately, we expect to see increased academic persistence and achievement among HOP program completers.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Up To Me Intervention + No Booster
  • Behavioral: Up To Me Intervention + Booster
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
201 participants
Allocation:
Randomized
Intervention Model:
Sequential Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Up To Me: Erasing the Stigma of Mental Illness on College Campuses
Actual Study Start Date :
Mar 7, 2022
Anticipated Primary Completion Date :
Mar 30, 2024
Anticipated Study Completion Date :
Mar 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention + No Booster

This arm will have n=67 participants. The Up To Me behavioral intervention will be administered via 2-hour sessions over three consecutive weeks. During these sessions, participants will complete worksheets from the Up To Me workbook.

Behavioral: Up To Me Intervention + No Booster
Participants will complete two-hour sessions once a week over three weeks in which they complete modules in the Up To Me Workbook. These sessions are facilitated by a peer facilitator and a member of the USF Counseling center. Other members in the group sessions are university students who are peers who are also experiencing some form of shame around their mental health challenges.

Experimental: Intervention + Booster

This arm will have n=67 participants. The Up To Me behavioral intervention will be administered via 2-hour sessions over three consecutive weeks. During these sessions, participants will complete worksheets from the Up To Me workbook. Additionally, participants randomized to this arm will complete an additional session 4 weeks after the third session of the intervention.

Behavioral: Up To Me Intervention + Booster
In addition to the Up To Me Intervention, participants also complete a booster/additional session where additional topics of the Up To Me workbook are covered. This additional session occurs four weeks after the completion of the third session.

No Intervention: Waitlist Control

This arm will have n=67 participants. Those randomized to this arm will be engaged in "treatment as usual", participating in the same services and activities that they were engaged with prior to recruitment into the study.

Outcome Measures

Primary Outcome Measures

  1. Self-Stigma of Mental Illness Scale-Short Form [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    Scores correspond with the four stage regressive model of self-stigma. The min of this scale is 1 or "I strongly disagree" and the max is 9 or "I strongly agree". Using this scale, an observed decrease would be a better outcome.

  2. Stigma Stress Scale [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    This scale includes 4 items measuring appraisal of stigma as a stressor (e.g., "prejudice against people with mental illness will have a negative impact on my future") and 4 items measuring perceived resources to cope with stigma (e.g., "I am prepared to deal with prejudice against people with mental illness"). The min on the scale is 1 or "Strongly disagree" to 7 or "Strongly agree". Using this scale, an observed increase would be a better outcome.

  3. Why Try Stigma Scale (WTSS) [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    The current version of the WTSS does not include items specific to the pursuit of postsecondary education. Therefore, the investigators will add two items for the purpose of this study: "I am not worthy of obtaining a college degree because I have a mental illness" and "I am not capable of obtaining a college degree because I have a mental illness." After the addition of the two aforementioned items, this scale includes 16 items on a seven-point agreement scale. The min on the scale is 1 or "Strongly disagree" to 7 or "Strongly agree". Using this scale, an observed decrease would be a better outcome.

  4. The Empowerment Scale [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    Yields five factors: self-efficacy/self-esteem, power/powerlessness/community activism, righteous anger, and optimism/control over the future. This scale includes 28 items on a 4-point agreement scale. The min on the scale is 1 or "Strongly Disagree" to the max of 4 or "Strongly Agree". Using this scale, an observed increase would be a better outcome.

  5. Self-Determination Scale [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    Participants respond to a vignette about a person, Harry, living with schizophrenia. The scale includes 14 items on a 9-point agreement scale. The minimum on the scale is 1 or "Strongly Agree" to 9 or "Strongly Disagree". Using this scale, an observed decrease would be a better outcome.

Secondary Outcome Measures

  1. College Student Experiences Questionnaire (CSEQ Fourth Edition) [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    Following the design of the study conducted by Salzer examining the postsecondary experiences of students with psychiatric disabilities, the investigators will administer several scales from the CSEQ. The CSEQ assesses student campus experiences and engagement, relationships with others on campus, and the degree of satisfaction with their experience at a particular institution. Three indicators of academic integration will be included in this study. The first, Quality of Effort (QE), refers to the underlying assumption of the CSEQ: "The more effort students expend in using the resources and opportunities an institution provides for their learning and development, the more they benefit." This scale has 22 items on a 4-point frequency scale. The minimum on the scale is 1 or "Never" to the max (4) or "Very Often". Using this scale, an observed increase would be a better outcome.

  2. Peer Group Interactions Scale [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    The Peer-Group Interactions Scale is a subscale of Pascarella and Terenzini's scale assessing the academic and social considerations in student persistence. This scale has 7 items on a 7-point agreement scale. The min on the scale is 1 or "Strongly Disagree" to the max (7) or "Strongly Agree". Using this scale, an observed increase would be a better outcome.

  3. Interactions with Faculty Scale [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    The Interactions with Faculty Scale is a subscale of Pascarella and Terenzini's scale assessing the academic and social considerations in student persistence; this scale focuses on assessing the quality of faculty interactions. This scale has 5 items on a 7-point agreement scale. The min on the scale is 1 or "Strongly Disagree" to the max (7) or "Strongly Agree". Using this scale, an observed increase would be a better outcome.

  4. Sense of Campus Belonging Scale (SoCB) [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    Sense of belonging is a psychological construct unique from engagement and integration, focusing on students' subjective feelings of connectedness. Hurtado and Carter developed a measure of cohesion including a subscale of sense of belonging including items concerning perceived "belonging," "fit," and being a "part" of the community. Each of the three items on the SoCB scale is rated on an 11-point Likert scale with a min of 0 or "Strongly DIsagree to the max (10) "Strongly agree". Using this scale, an observed increase would be a better outcome.

  5. Attitudes Towards Seeking Professional Psychological Help Scale (ATSPPHS) [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    The Attitudes Towards Seeking Professional Psychological Help Scale measures attitudes towards seeking help for mental health concerns from professional sources. This scale has 10 items on a 4-point agreement scale with a min of 1 or "Disagree" to a max of 4 "Agree". Using this scale, an observed increase would be a better outcome.

  6. Actual Help Seeking Questionnaire [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    The Actual Help Seeking Questionnaire (AHSQ) assesses recent help-seeking behavior and was adapted from Rickwood and Braithwaite. The AHSQ has been successfully used to measure help-seeking across different time contexts, sources of help, and types of problems. Recent help-seeking behavior is determined by listing a number of potential help sources and asking whether or not help has been sought from each of the sources during a specified period of time for a specified problem. This questionnaire has 14 items that represent sources of help-seeking. Using this questionnaire, an observed increase in sources used would be a better outcome.

  7. Grade Point Average (GPA) [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    GPA will be retrieved from University records at all measurement time points (baseline, post-test, and 1, 3, and 6- month follow-up). Students will be asked to sign a release form consenting that their GPA records be released to the study investigators. The investigators do realize GPA may lack sensitivity to change over time, however, the investigators include this variable as previous research in higher education has captured change over relatively short time periods (one to two years).

  8. Academic and Intellectual Development Scale [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    The Academic and Intellectual Development Scale is a subscale of Pascarella and Terenzini's scale assessing the academic and social considerations in student persistence; it focuses on assessing satisfaction with the institution's academics. This scale has 7 items on a 7-point agreement scale with a min of 1 or "Strongly Disagree" to a max of 7 or "Strongly Agree". Using this scale, an observed increase would be a better outcome.

  9. Academic Persistence [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    Data on student registration status will be retrieved from University records at all measurement time points. Data on actual persistence will be coded: 1= withdrawal, 2= persisted. The investigators will ask students to sign a release consenting that their enrollment records be released to the study investigators. Intent to persist will be measured using a single item: "It is likely that I will re-enroll in the university next semester" (5= strongly agree, 1= strongly disagree). An observed increase would be a better outcome. In order to capture persistence and achievement over the entire course of the project (after 6-month follow-up is complete, The investigators will continue to collect data from the University records at five-month intervals (approximately once every semester) until the end of the project period. The investigators will request consent from all students to access these records.

  10. Counseling Center Assessment of Psychological Symptoms [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    Collecting this data will allow us to control for symptom severity in our analyses. These measures were selected as they have strong psychometric properties and sensitivity to change, require minimal time to complete, and are also the assessments administered to all students receiving services at USF where the study will take place.

  11. Diagnostic and Status Questionnaire [This measure will be collected at week 0 for all participants]

    In addition to the Counseling Center tools, the investigators will provide the opportunity for participants to self-report diagnosis and disability. This tool was developed by the National Center for Science Education for patient self-report. This questionnaire assesses impairment symptoms on a 7-point scale with a min of 1 or "Not at all impaired" to a max of 7 (Very much impaired). Using this scale, a low score would be a better outcome.

  12. Diagnostic and Status Questionnaire Past 4 weeks [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    In addition to the Counseling Center tools, the investigators will provide the opportunity for participants to self-report diagnosis and disability. This tool was developed by the National Center for Science Education for patient self-report. This questionnaire assesses impairment symptoms on a 7-point scale with a min of 1 or "Not at all impaired" to a max of 7 (Very much impaired). Using this scale, an observed decrease would be a better outcome.

  13. Behavioral Health Measure [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    Collecting this data will allow us to control for symptom severity in our analyses. These measures were selected as they have strong psychometric properties and sensitivity to change, require minimal time to complete, and are also the assessments administered to all students receiving services at USF where the study will take place. This measure has 20 items on a 5-point scale with a min 0 and a max of 5. For seven items, a score of 5 is a high and positive rating. For these items, an observed increase over time would be a better outcome. For the remaining items, a score of 5 is a high rating of distress and an observed decrease would be a better outcome.

  14. Recovery Assessment Scale [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    The Recovery Assessment Scale (RAS) is a 24-item measure based on a process model of recovery, the RAS attempts to assess aspects of recovery with a special focus on hope and self-determination. These items are measured on a 5-point agreement scale with a min of 1 or "strongly disagree" to a max of 5 or "strongly agree". Using this scale an observed increase would be a better outcome.

  15. Quality of Relationships Scale [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    A 3-item scale that measures the quality of an individual's relationship with a specific person. Items are measured on a 7-point rating scale with a min of 1 and max of 7. Where 1 is a low rating of the relationship quality and 7 is a high rating. An observed increase would be a better outcome.

  16. Up To Me Satisfaction Scale [This measure will be collected at week 7 if in the Up To Me Intervention + Booster or Up To Me Intervention + No Booster arms]

    This scale assesses participants' satisfaction with and feedback for the team regarding the primary intervention of the study. This measure is not being used to measure observed changes. The investigators are interested in the participants' satisfaction with the intervention. This scale includes 6 items on a 7-point agreement scale with a min of 1 or "Highly Agree" and a max of 7 or "Highly Disagree".

  17. Demographics Questionnaire [This measure will be collected at week 0 for all participants]

    Provides background information on participants regarding their identities and experiences. This questionnaire is not being used to measure observed changes but to describe the study sample.

  18. Peer Support and Advocacy Items [Change from baseline to week 3, week 7, week 15 and 27 for all participants]

    This scale was developed by the study investigators and is comprised of four items inquiring about the participant's involvement in organizations related to peer support or advocacy for mental illness. An observed increase in involvement would be a better outcome.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • College students enrolled at USF

  • Over 18 years of age

  • Individuals with psychiatric disability(ies) who feel shame regarding their mental illness or keep it secret

Exclusion Criteria:
  • Individuals with a sole substance abuse disorder

  • Individuals who plan to graduate before the conclusion of the data collection period; for intervention participants, this would be a graduation date within 6 months of starting the intervention.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of South Florida Tampa Florida United States 33620

Sponsors and Collaborators

  • University of South Florida
  • National Institute on Disability, Independent Living, and Rehabilitation Research
  • Temple University
  • Illinois Institute of Technology

Investigators

  • Principal Investigator: Kristin Kosyluk, University of South Florida

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University of South Florida
ClinicalTrials.gov Identifier:
NCT05784818
Other Study ID Numbers:
  • 90IFRE0056-01-00
First Posted:
Mar 27, 2023
Last Update Posted:
Mar 27, 2023
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of South Florida
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 27, 2023