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Behavioral Intervention

HOP Program for Mental Illness

N/A
Recruiting
Led By Nicolas Rüsch, Dr.
Research Sponsored by University of Ulm
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
At least a moderate level of self-reported disclosure-related distress/difficulty (score 4 or higher on the screening item 'In general, how distressed or worried are you in terms of secrecy or disclosure of your mental illness to others?', rated from 1, not at all, to 7, very much)
Age 18 or above
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 3, 6 and 12 weeks (t3)
Awards & highlights

Study Summary

This trial will test a new group intervention for soldiers with mental illness to see if it is effective.

Who is the study for?
This trial is for soldiers and first responders in Berlin, Germany who are fluent in German, aged 18 or above, currently receiving mental health treatment, and experiencing distress about disclosing their mental illness. They must have a diagnosed mental disorder but not solely substance-related disorders.Check my eligibility
What is being tested?
The 'Honest, Open, Proud' program is being tested to see if it helps soldiers with mental illnesses feel better about discussing their condition. It's a group-based intervention designed to reduce the discomfort associated with talking about one's own mental health issues.See study design
What are the potential side effects?
Since 'Honest, Open, Proud' is a psychological support program rather than a medication or medical procedure, traditional side effects are not applicable. However, participants may experience emotional discomfort or increased anxiety when confronting issues related to their illness.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I feel moderately to very distressed about sharing my mental illness with others.
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I am 18 years old or older.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 3, 6 and 12 weeks (t3)
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, 3, 6 and 12 weeks (t3) for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Stigma Stress Scale, 8 items
WHOQoL BREF; Domain psychological quality of life, 6 items
Secondary outcome measures
Attitudes to disclosure, 2 items
Attitudes to help-seeking, 2 items
Disclosure related distress ("In general, how distressed or worried are you in terms of secrecy or disclosure of your mental illness to others?', from 1, not at all, to 7, very much)
+8 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Honest, Open, ProudExperimental Treatment1 Intervention
The group program is about disclosure versus secrecy of one's mental illness. The groups are facilitated by two peers (soldiers with lived experience of mental illness). Each group runs for three weeks, one meeting per week, and two hours per meeting. There is one 2-hour booster session in week 6. Fidelity to manual: rated by a research assistant who is present during the group session
Group II: Control groupActive Control1 Intervention
Treatment as usual (TAU)

Find a Location

Who is running the clinical trial?

University of UlmLead Sponsor
182 Previous Clinical Trials
66,715 Total Patients Enrolled
1 Trials studying Mental Health Disorders
1,000 Patients Enrolled for Mental Health Disorders
Center for Military Mental Health, Berlin, GermanyUNKNOWN
Illinois Institute of Technology, Chicago, USAUNKNOWN
1 Previous Clinical Trials
100 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there currently any opportunities to enrol in this experiment?

"This medical trial, which was first listed on November 15th 2017, is not currently recruiting. Its latest update was posted on December 1st 2020 and it has since been discontinued; however, 385 other studies are actively enrolling patients right now."

Answered by AI

What is the focus of this clinical trial's aims?

"This clinical trial has been devised to measure the World Health Organisation Quality of Life BREF Domain psychological quality of life, with 6 items assessed over a 3 week period. Secondary endpoints involve Ryff's 1989 Psychological Well-Being Scale (18 items), Boyd et al.'s 2014 Internalized Stigma of Mental Illness Inventory Brief Version (10 items) and Link et al.'s 1991 Secrecy and Social Withdrawal subscales from the Stigma Coping Orientation Scales (12 items)."

Answered by AI
~13 spots leftby Apr 2025