- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05284123
The Impact of a Self-Compassion Intervention on Shame and Mental Health Treatment-Seeking
April 8, 2024 updated by: Allison Kelly, University of Waterloo
The Impact of a Brief Self-Compassion Intervention on Shame and Mental Health Treatment-Seeking Among Distressed University Students
Untreated mental health problems can cause lasting harm to self-esteem, relationships, academics, productivity, and health.
It is thus highly worrisome that only 18-36% of university students with significant mental health problems seek help.
Many university campuses have responded to this mental health crisis by trying to increase students' mental health literacy (MHL), defined as "knowledge and beliefs about mental disorders which aid their recognition, management, or prevention''.
Increasing MHL appears to increase knowledge about mental health services, but it does not increase actual treatment-seeking desire or action.
One problem with this approach is that it falsely assumes that students struggling with their mental health will want to pursue services once they have learned more about mental disorders and the associated treatments available.
However, most people with mental disorders do not initially recognize that they have a disorder and may dismiss information about mental disorders and mental health treatment as irrelevant.
Feelings of shame are elevated in individuals with psychological disorders, and these feelings act as one of the strongest barriers to mental health treatment-seeking.Given the low rate of treatment-seeking on university campuses, research is needed to explore how best to facilitate mental health treatment seeking among distressed students, including those who may not self-identity as having a mental health problem.
Research has yet to examine the potential role of self-compassion in relation to treatment-seeking behaviours.
Self-compassion (SC) is conceptualized as responding to personal distress with gentleness and kindness in order to alleviate it, and it is negatively associated with shame.
However, research has not yet explored whether the perceived benefits of SC in mitigating shame can affect mental health treatment-seeking outcomes.
We propose that cultivating SC amongst psychologically distressed students will subsequently decrease shame, and thus, indirectly elevate willingness to seek mental health treatment.
Thus, this study will examine the effects of a one-session SC workshop/intervention compared to a one-session MHL intervention on shame and mental health treatment-seeking.
Participants will be distressed students recruited from the University of Waterloo, and will be randomly assigned to the SC intervention, MHL intervention, or control intervention.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
The study will consist of four online surveys.
During the first survey (Part 1; baseline), participants will answer a set of questionnaires.
During the second survey (Part 2; 1-4 days after Part 1), participants will first answer a set of questionnaires.
Then, they will be randomized to a self-compassion intervention, a mental health literacy intervention, or a control intervention.
Then, participants will answer more questionnaires immediately after completing the intervention.
During the third survey (Part 3; 14-17 days after Part 2) and fourth survey (Part 4; 3 months-3 months+7 days after Part 2), participants will answer a set of questionnaires.
Study Type
Interventional
Enrollment (Actual)
265
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 Contact
- Name: Giselle Kraus, MSc
- Phone Number: 519-888-4567
- Email: self.attitudes.lab@uwaterloo.ca
Study Locations
-
-
Ontario
-
Waterloo, Ontario, Canada, N2L3G1
- University of Waterloo
-
-
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
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Undergraduate student at University of Waterloo with a SONA account
- Scored 8+ on Kessler Psychological Distress Scale (K6; screener scale)
Exclusion Criteria:
- None
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Self-compassion intervention
Brief (20-minute) workshop with a self-compassion writing exercise and information about mental health resources available to students.
|
The self-compassion workshop instructs participants to reflect on a source of shame, connect with their suffering related to it, and then direct feelings of support and understanding towards their suffering via a few brief writing tasks.
This workshop also provides participants with basic information about mental health resources.
|
Experimental: Mental health literacy intervention
Brief (20-minute) workshop with information and a written reflection about common mental disorders, and information about mental health resources available to students.
|
The mental health literacy workshop provides participants with information about the symptoms and treatment of common mental disorders, and asks participants to reflect on what they learned through a couple brief writing tasks.
This workshop also provides participants with basic information about mental health resources.
|
Active Comparator: Control
Brief (7-minute) workshop with information about mental health resources available to students.
|
The control workshop provides participants with basic information about mental health resources.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
State Shame and Guilt Scale (shame subscale)
Time Frame: Change from pre-intervention to immediately post-intervention
|
Self-report questionnaire with 5 questions on a 5-point Likert scale (scored 1-5).
Total scores range from 5-25, with higher decrease in score indicative of less momentary shame.
|
Change from pre-intervention to immediately post-intervention
|
Experience of Shame Scale
Time Frame: Change from baseline to 2 weeks and 3 months post-intervention
|
Self-report questionnaire with 25 questions on a 4-point Likert scale (scored 1-4).
Total scores range from 25-100, with higher decrease in score indicative of less shame.
|
Change from baseline to 2 weeks and 3 months post-intervention
|
Treatment-seeking intention questions (researcher-generated)
Time Frame: Change from baseline to immediately, 2 weeks, and 3 months post-intervention
|
4 self-report questions to assess changes in intentions of seeking mental health treatment or resources.
|
Change from baseline to immediately, 2 weeks, and 3 months post-intervention
|
Treatment-seeking behaviours questions (researcher-generated)
Time Frame: Change from baseline to immediately, 2 weeks, and 3 months post-intervention
|
5 self-report questions to assess changes in mental health treatment-seeking behaviours.
|
Change from baseline to immediately, 2 weeks, and 3 months post-intervention
|
Distress Disclosure Index
Time Frame: Change from baseline to immediately, 2 weeks, and 3 months post-intervention
|
Self-report questionnaire with 12 questions on a 5-point Likert scale (scored 1-5).
Total scores range from 12-60, with higher increase in score indicative of greater distress disclosure.
|
Change from baseline to immediately, 2 weeks, and 3 months post-intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Compassionate Engagement and Action Scale (adapted self-compassion subscale)
Time Frame: Immediately post-intervention
|
Self-report questionnaire with 13 questions on a 10-point Likert scale (scored 1-10).
Three questions are reverse-scored and not included in scoring.
Total scores range from 10-100, with higher score indicative of greater momentary emotional engagement during intervention.
|
Immediately post-intervention
|
Kessler Psychological Distress Scale (K6)
Time Frame: Change from baseline to 2 weeks and 3 months post-intervention
|
Self-report questionnaire with 6 questions on a 5-point Likert scale (scored 0-4).
Total scores range from 0-24, with higher decrease in score indicative of less psychological distress.
|
Change from baseline to 2 weeks and 3 months post-intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Allison Kelly, PhD, University of Waterloo
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)
November 12, 2021
Primary Completion (Estimated)
May 31, 2024
Study Completion (Estimated)
May 31, 2024
Study Registration Dates
First Submitted
March 8, 2022
First Submitted That Met QC Criteria
March 8, 2022
First Posted (Actual)
March 17, 2022
Study Record Updates
Last Update Posted (Actual)
April 10, 2024
Last Update Submitted That Met QC Criteria
April 8, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 42483
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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