- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06402929
Honest, Open, Proud - College for Post-Secondary Students with Mental Health Challenges
Self-stigma and Strategic Disclosure Amongst Canadian Postsecondary Students
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Mental health issues have been highlighted as a growing concern within the post-secondary student population. Studies show that one significant concern for post-secondary students pertains to disclosing their mental challenges to others. Disclosure decisions are especially relevant for postsecondary students in the context of academic and social support. Students with mental health challenges who do not receive helpful accommodations may experience greater stress related to academics. Students also note that, in navigating their social sphere, they often need to consider what aspects of their mental health challenges to share in what situations.
As such, students often need to make decisions about whether to conceal or disclose their mental health challenges, both of which have their own pros and cons. Disclosure is a complex decision that requires consideration of personal and contextual factors. Honest, Open, Proud-College (HOP-C) is a peer-led, group-based intervention, that supports post-secondary students in the process of making decisions to disclose their mental health conditions. This study will evaluate the impacts of HOP-C administered through a videoconferencing platform on personal, social, and disclosure related outcomes.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Ontario
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Thunder Bay, Ontario, Canada
- Lakehead University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age 17 to 29 years old
- Enrolment in an university or college in Canada
- Self-identify as experiencing mental health challenges
- Moderate level of self-reported self-stigma (score 4 or higher on the screening item "Do you feel ashamed about dealing with anxiety, depression, or any other mental health challenges?", rated from 1, not at all, to 7, very much)
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Honest Open Proud - College (HOP-C)
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The program consists of three weekly workshops that are two hours in duration. There is a fourth booster workshop (two hours in duration) one month following program completion. All workshops will be held over an online videoconferencing platform. HOP-C is a group program led by trained peer facilitators who have lived mental illness experience. Major topics that the program covers are:
During the booster workshop, participants will be encouraged to reflect on their disclosure decisions, and periodically revisit their disclosure cost-benefit analysis in deciding if and when to disclose in the future. |
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No Intervention: Waitlist Control
Participants randomized to the waitlist control condition complete the study measures at the same timepoints as the experimental group while remaining on a waiting list for the program.
Following this, participants randomized to the waitlist are invited to participate in HOP-C without completing study measures.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Self-Stigma of Mental Illness Scale-Short Form (Corrigan et al., 2012)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
|
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Attitudes to Disclosure Questionnaire (Mayer et al., 2022)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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Empowerment Scale (Rogers et al., 1997)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Stigma Stress Scale (Rüsch, Corrigan, Powell, et al., 2009; Rüsch, Corrigan, Wassel, et al., 2009)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
|
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Rosenberg Self-Esteem Scale (Rosenberg, 1965)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
|
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Self-Efficacy about Disclosure Scale (Conley et al., 2019; Rüsch et al., 2014)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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Multidimensional Scale of Perceived Social Support (Zimet et al., 1988)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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General Help Seeking Questionnaire (Wilson et al., 2005)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
|
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Actual Help Seeking Questionnaire (Rickwood et al., 2005)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Depression-Anxiety-Stress Scale-21 (DASS-21; Lovibond & Lovidbond, 1995)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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|
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Online Experience Questionnaire
Time Frame: Post Intervention (3 weeks)
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Assesses participants' experience with HOP-C in an online format.
Consists of 10 items asking about comfortability and presentation of session content over the video conferencing platform.
There is an additional question welcoming other comments and concerns.
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Post Intervention (3 weeks)
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Disclosure Worksheet
Time Frame: Post Intervention (3 weeks) and Post Booster (7 weeks)
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Assess disclosure behaviours using the "Details of Your Disclosure- How Did it Go?" Worksheet in the HOP-C manual.
This worksheet collects information on whether the participant disclosed, who they disclosed to, and the participant's self-reported satisfaction with the exchange and the positivity of the exchange.
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Post Intervention (3 weeks) and Post Booster (7 weeks)
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 1468496
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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