To Share Or Not To Share (2Share)
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| ClinicalTrials.gov Identifier: NCT03943862 |
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Recruitment Status :
Terminated
(The study was terminated due to a small number of study participants.)
First Posted : May 9, 2019
Last Update Posted : March 13, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| History of Suicide Attempt | Behavioral: 2Share | Phase 2 |
People who have survived a suicide attempt often face public and self-stigma, and secrecy is a common strategy to minimize the risk of being labeled. Both secrecy and disclosure have pros and cons. The decision whether, when, and to whom to disclose a previous suicide attempt is complex. Interventions can provide guidance for systematic consideration and a well informed decision. Potentially, it may not be disclosure itself, but the empowered decision for or against disclosure of a previous suicide attempt that reduces distress and leads to beneficial outcomes.
The manualized peer-led group intervention "Honest, Open, Proud" (HOP) supports people with mental illness in their decision whether to disclose mental illness. Research showed positive effects of the intervention on stigma stress, disclosure-related distress and quality of life. Based on HOP, "To Share Or Not To Share" (2Share) was developed to systematically guide suicide attempt survivors through their decision whether and how to disclose a previous suicide attempt.
2Share led to significant reductions in self-stigma and depressive symptoms, as well as increased self-esteem in a recent pilot randomized-controlled trial (RCT) in the US. The aim of the current study is to evaluate 2Share in a German clinical setting. Feasibility and efficacy of 2 Share will be tested in a pilot RCT.
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 4 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | To Share or Not To Share (2Share) - Group Intervention to Support Disclosure Decisions After Suicide Attempt |
| Actual Study Start Date : | May 7, 2019 |
| Actual Primary Completion Date : | January 1, 2020 |
| Actual Study Completion Date : | March 1, 2020 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Intervention (2Share) + treatment as usual
Study participants randomized to the experimental group receive the intervention (2Share) while maintaining their current treatment (treatment as usual). 2Share is a peer-led group intervention containing three two-hour sessions within two weeks plus an additional booster session four weeks later. Fidelity to manual is rated in each session by study staff. |
Behavioral: 2Share
The peer-led group program contains of three lessons plus one booster session:
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No Intervention: Treatment as usual
Participants randomized to the control group do not receive the group program but maintain their current treatment (treatment as usual).
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- Self-stigma related to suicide attempt [ Time Frame: 2 weeks ]Self-Stigma of Suicide Attempt Survivor Scale (SSSAS), 14-item apply subscale (Sheehan et al, 2018); each item is rated from 1-9, we will calculate a sum score accross all items (range 9-126) with higher scores indicating more self-stigma.
- Self-stigma related to suicide attempt [ Time Frame: baseline, 6 weeks, 12 weeks ]Self-Stigma of Suicide Attempt Survivor Scale (SSSAS), 14-item apply subscale (Sheehan et al, 2018); each item is rated from 1-9, we will calculate a sum score accross all items (range 9-126) with higher scores indicating more self-stigma.
- Self-Stigma (alienation) related to suicide attempt [ Time Frame: baseline, 6 weeks, 12 weeks ]Internalized Stigma of Mental Illness scale (ISMI), 6-item alienation subscale (Ritsher et al. 2003) adapted for suicide attempt, 6 items rated from 1-4, we will calculate a mean score accross all items (range: 1-6) with higher scores indicating more self-stigma.
- Stigma stress related to suicide attempt [ Time Frame: baseline, 2 weeks, 6 weeks, 12 weeks ]Stigma Stress Scale (Rüsch et al., 2009a,b) adapted for suicide attempt, 8-items rated from 1-7 with 4 items measuring the primary appraisal of stigma as harmful and 4 items measuring the secondary appraisal of perceived resources to cope with stigma-related harm, for each of the two subscales we will calculate a mean score (range 1-7) and a total stigma stress score will be caclulated by subtracting perceived resources from perceived harm with higher difference scores (range -6 to +6) indicating more stigma-stress.
- Secrecy about suicide attempt [ Time Frame: baseline, 2 weeks, 6 weeks, 12 weeks ]Secrecy Scale (Link et al., 1991) adapted for suicide attempt, 5 items rated from 1-6, we will calculate a mean score accross all items (range 1-6) with higher scores indicating more secrecy.
- General disclosure distress [ Time Frame: baseline, 2 weeks, 6 weeks, 12 weeks ]Distress Disclosure Index (Kahn et al., 2001), 12 items rated from 1-5, we will calculate a sum score accross all items (range 12-60) with higher scores indicating more disclosure distress.
- Help-seeking for suicidality [ Time Frame: baseline, 2 weeks, 6 weeks, 12 weeks ]General Help-Seeking Questionnaire - suicidal ideation subscale (GHSQ-SI) (Wilson et al., 2005), 10 items rated from 1-7, we will calculate mean scores (range 1-7) for items related to social contacts (items 1-4) and care providers (items 5,7,10).
- Depressive symptoms [ Time Frame: baseline, 2 weeks, 6 weeks, 12 weeks ]Center for Epidemiological Studies-Depression Scale - short form (CES-D) (Hautzinger et al., 1993), 15 items rated from 0-3, we will calculate a sum score accross all items (range 0-45) with higher scores indicating more depressive symptoms.
- Suicidal ideation [ Time Frame: baseline, 2 weeks, 6 weeks, 12 weeks ]Suicidal Ideation Attributes Scale (SIDAS) (Spijker et al., 2014), 5 items rated from 0-10, we will calculate a total sum score accross all items (range 0-50) with higher scores indicating more suicidality.
- Recovery [ Time Frame: baseline, 2 weeks, 6 weeks, 12 weeks ]Recovery Assessment Scale - short version (RAS-G) (Corrigan et al., 2004), 24 items rated from 1-5, we will calculate a mean score accross all items (range 1-5) with higher scores indicating more recovery.
- Self-esteem [ Time Frame: baseline, 2 weeks, 6 weeks, 12 weeks ]Rosenberg's Self-Esteem Scale (RSE) (Collani et al., 2003), 10 items rated from 0-3, we will caculate a sum score accross all items (range 0-30) with higher scores indicating more self-esteem.
- Quality of life [ Time Frame: baseline, 2 weeks, 6 weeks, 12 weeks ]EUROHIS Quality of Life Index (EUROHIS-QOL) (Brähler et al., 2007), 8 items rated from 1-5, we will calculate a sum score accross all items (range 8-40) with higher scores indicating more quality of life.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Current inpatient, outpatient or day clinical treatment at the Bezirkskrankenhaus Günzburg, Germany
- Age ≥ 18 years
- At least one previous suicide attempt
- Positive screening for disclosure distress (1 item: "In general, how distressed or worried are you in terms of secrecy or disclosure of your suicide attempt?", self-report, persons with a score ≥ 4 on a scale from 1-7 are included)
- Written informed consent
- Sufficient German language skills
Exclusion Criteria:
- Current suicidality (1 item: "Have you had thoughts that you would be better off dead for at least several days during the last week?", self-report, persons responding with yes will be excluded and will be offered support)
- Suicide attempt within the last four weeks
- Dementia or organic disease (ICD-10: F0)
- Primary substance dependence (ICD-10: F1x.2)
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03943862
| Germany | |
| University of Ulm and BKH Günzburg | |
| Ulm, Germany, 89073 | |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Nathalie Oexle, Assistant Professor, University of Ulm |
| ClinicalTrials.gov Identifier: | NCT03943862 |
| Other Study ID Numbers: |
345/18 |
| First Posted: | May 9, 2019 Key Record Dates |
| Last Update Posted: | March 13, 2020 |
| Last Verified: | March 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Stigma Suicide attempt survivor Secrecy Group intervention Disclosure |
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Suicide Suicide, Attempted Self-Injurious Behavior Behavioral Symptoms |

