Pilot Study on Follow-Up of (Acutely) Suicidal Individuals From the Flemish Suicide Helpline, Zelfmoordlijn 1813, to Promote Continuity of Care

NCT ID: NCT07343258

Last Updated: 2026-01-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

98 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-01-01

Study Completion Date

2026-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This pilot study aims to assess the acceptance, feasibility, and added value of follow-up calls at the suicide helpline, Zelfmoordlijn 1813, in Flanders (Belgium). It serves as a crucial preparatory step in the development and implementation process of the callback methodology at Zelfmoordlijn 1813.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

International research confirms the importance of suicide prevention helplines. They offer immediate crisis support and try to guide people toward appropriate assistance. In practice, however, many callers do not follow up on referrals. Barriers such as costs, waiting times, or insufficient motivation play a role in this. Although call responders mainly offer emotional support, one conversation is often not enough to go into depth on concrete strategies or referrals. Nevertheless, in addition to offering a listening ear, helplines can play a crucial role in motivating and activating callers to seek further help.

The effectiveness of an initial crisis intervention is strongly related to the extent to which it is embedded in a broader care process. That is why there is growing international attention for systematic follow-up after an initial call to a helpline. International studies convincingly show that follow-up conversations after a crisis call have positive effects. Follow-up calls offer extra support, help people take the step towards (professional) help, and reinforce self-care strategies. In the United States, such calls were funded and organized by the health service SAMHSA. In Ireland, research showed that people who were called back after an initial call were significantly less likely to die by suicide than people who did not receive follow-up. In a large-scale American study, nearly 80% of suicidal callers said that the follow-up calls had helped them prevent suicide. More than 90% felt safer afterwards. People at acute risk of suicide in particular reported benefiting from the calls, which they found motivating and protective. Multiple and longer follow-up calls were associated with a stronger sense of safety and a lower estimated risk of suicide. Elements such as safety planning and strengthening social support proved to be decisive in this regard.

In this context, the Flemish Expertise Center for Suicide Prevention (VLESP, Ghent University), in collaboration with the Center for Suicide Prevention (CPZ), is investigating whether and how telephone follow-up calls are feasible for adult callers to the Zelfmoordlijn 1813 who are at (acute) risk of suicide. This is an exploratory pilot study that examines whether this form of follow-up is practically feasible and what added value it can offer as a supplement to the existing services. In this pilot study, CPZ staff members, known as callback callers, conduct callback conversations with a limited group of callers who have previously contacted the Zelfmoordlijn 1813 and given their consent to be called back for research purposes. The callback method provides for a maximum of three callback conversations per person, each of which responds to the individual needs of the caller. The callback method distinguishes between three callback profiles: safety conversation, safety planning, and continuity of care.

During this pilot study, callers are recruited with the help of a limited group of experienced volunteers from the Zelfmoordlijn 1813. These volunteers remain anonymous to the outside world and play a central role in the recruitment process. During the telephone conversation, they assess whether the caller meets the selection criteria for participation in the callback study. If the caller is 18 years of age or older, is calling from a personal telephone, and could benefit from a callback, the caller is invited to participate in the study.

Qualitative interviews with both callers and callback callers and focus groups with call responders are used to assess how the callback method is perceived. Aspects such as acceptance, feasibility, and perceived added value are examined. The interviews with callers and callback callers each last approximately one hour. Conversations with callers take place by telephone, while interviews with callback callers are conducted at the CPZ office. The focus groups with call responders last approximately two hours. Responders can choose to participate in an online session or a physical meeting at the CPZ office. A total of between 53 and 98 persons will participate in the study, namely: 3 callback callers from the CPZ, 20 call responders from the Zelfmoordlijn 1813, and between 30 and 75 participating callers.

The findings from this pilot study will serve as a basis for further refining the callback methodology at Zelfmoordlijn 1813 and, if regarded as positive, preparing for broader implementation.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Suicide Suicidal Ideation and Behavior Crisis Intervention

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Callers, responders and callback callers involved in callback conversations at Suicide Line 1813

The main target group of this research are (acutely) suicidal individuals who contact Zelfmoordlijn 1813 by phone and consent to receive callback conversations followed by an interview to share their experiences.

During the pilot study, a number of experienced call responders (i.e., trained volunteers of the Zelfmoordlijn 1813 who offer callers a callback trajectory) and callback callers (i.e., staff members of the CPZ who conduct the callback conversations) apply the callback methodology developed by the CPZ. Call responders and callback callers will also be interviewed to provide further insights into the callback methodology.

Group Type EXPERIMENTAL

Callbacks from the Zelfmoordlijn 1813

Intervention Type OTHER

Callers of Zelfmoordlijn 1813 are called back after their initial conversation, in which they themselves contacted the Zelfmoordlijn 1813. The callbacks focus on crisis management at the Zelfmoordlijn 1813 and are not intended as a form of formal support. During the callback calls, the specific needs of the caller are addressed, tailored to the callback profile assigned by a call responder based on the initial call. There are three different callback profiles for callers: (1) those for whom the crisis call immediately focuses on creating safety, with the callback calls further reinforcing this safety, (2) those for whom the focus is on crisis management, with follow-up aimed at developing and implementing a Safety Plan, and (3) those who experience barriers to discussing their suicidal thoughts, with the callback conversations being used to facilitate the step towards professional help or to make suicide discussable within their own network or existing support services.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Callbacks from the Zelfmoordlijn 1813

Callers of Zelfmoordlijn 1813 are called back after their initial conversation, in which they themselves contacted the Zelfmoordlijn 1813. The callbacks focus on crisis management at the Zelfmoordlijn 1813 and are not intended as a form of formal support. During the callback calls, the specific needs of the caller are addressed, tailored to the callback profile assigned by a call responder based on the initial call. There are three different callback profiles for callers: (1) those for whom the crisis call immediately focuses on creating safety, with the callback calls further reinforcing this safety, (2) those for whom the focus is on crisis management, with follow-up aimed at developing and implementing a Safety Plan, and (3) those who experience barriers to discussing their suicidal thoughts, with the callback conversations being used to facilitate the step towards professional help or to make suicide discussable within their own network or existing support services.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* The caller is 18 years or older.
* The caller speaks Dutch.
* The caller calls the Zelfmoordlijn 1813 for themselves due to suicidal ideation.
* The caller must benefit from callback conversations fitting one of the three callback profiles.
* The caller is not a frequent caller to the Zelfmoordlijn 1813.
* The caller can be called back directly on a personal device.
* The caller is legally competent, meaning they can oversee the potential consequences of participation, such as time investment and availability.
* At the time of recruitment, the caller is not receiving support within a care trajectory where attention is paid to their suicidality. Or the care provider is not available quickly enough (e.g., due to maternity leave) if the caller falls within the callback profile focusing on a safety conversation.

Exclusion Criteria

* The caller is younger than 18 years.
* The caller does not speak Dutch.
* The caller does not call the Zelfmoordlijn 1813 for themselves.
* The caller is a frequent caller to the Zelfmoordlijn 1813.
* The call responder assesses that urgent medical help is necessary.
* The caller expresses a homocide threat during the original conversation to the Zelfmoordlijn 1813.
* The caller cannot be called back on a personal device (e.g., persons in detention).
* The caller is not legally competent to oversee the consequences of participation (e.g., under the influence of alcohol and/or drugs).
* At the time of recruitment, the caller is receiving support within a care trajectory where attention is paid to their suicidality.
2. Call responders The CPZ chooses to recruit call responders who have extensive experience in answering calls at the Zelfmoordlijn 1813. Therefore, not all call responders of the Zelfmoordlijn 1813 are trained to recruit callers.
3. Callback callers The staff members of the CPZ who are involved in developing and implementing the callback methodology will also participate in the research by means of an interview.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University Ghent

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Gwendolyn Portzky, PhD

Role: PRINCIPAL_INVESTIGATOR

University Ghent

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Flemish Centre of Expertise in Suicide Prevention, Ghent University

Ghent, , Belgium

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Belgium

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Eva De Jaegere, PhD

Role: CONTACT

+32 (0)9 332 07 75

Lore Bellaert, PhD

Role: CONTACT

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Eva De Jaegere, PhD

Role: primary

+32 (0)9 332 07 75

Lore Bellaert, PhD

Role: backup

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

ONZ-2025-0344

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.