Honest, Open, Proud - College for Post-Secondary Students with Mental Health Challenges

March 4, 2025 updated by: Lakehead University

Self-stigma and Strategic Disclosure Amongst Canadian Postsecondary Students

The purpose of the study is to evaluate the efficacy of an online format of the group-based intervention "Honest Open Proud-College" among Canadian post-secondary students.

Study Overview

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

Interventional

Enrollment (Actual)

63

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Ontario
      • Thunder Bay, Ontario, Canada
        • Lakehead University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

No

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
Experimental: Honest Open Proud - College (HOP-C)

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:

  1. discussing different types of disclosure;
  2. conducting a cost-benefit analysis of disclosing in different situations;
  3. strategies to anticipate how certain people will respond to disclosure when deciding on who to disclose to;
  4. disclosure via social media; and
  5. a guided creation of participants' own disclosure narrative.

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.

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.

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)
Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
Attitudes to Disclosure Questionnaire (Mayer et al., 2022)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
Empowerment Scale (Rogers et al., 1997)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)

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)
Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
Rosenberg Self-Esteem Scale (Rosenberg, 1965)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
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)
Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
Multidimensional Scale of Perceived Social Support (Zimet et al., 1988)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
General Help Seeking Questionnaire (Wilson et al., 2005)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
Actual Help Seeking Questionnaire (Rickwood et al., 2005)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Depression-Anxiety-Stress Scale-21 (DASS-21; Lovibond & Lovidbond, 1995)
Time Frame: Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
Baseline, Post Intervention (3 weeks), and Post Booster (7 weeks)
Online Experience Questionnaire
Time Frame: Post Intervention (3 weeks)
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.
Post Intervention (3 weeks)
Disclosure Worksheet
Time Frame: Post Intervention (3 weeks) and Post Booster (7 weeks)
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.
Post Intervention (3 weeks) and Post Booster (7 weeks)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 17, 2023

Primary Completion (Actual)

October 30, 2024

Study Completion (Actual)

October 30, 2024

Study Registration Dates

First Submitted

May 3, 2024

First Submitted That Met QC Criteria

May 3, 2024

First Posted (Actual)

May 7, 2024

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

March 4, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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