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Breaking Down Barriers to a Suicide Prevention Helpline

Primary Purpose

Suicidal Ideation

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Brief Barrier Reduction Intervention
Plain advisory text
Sponsored by
113 Suicide Prevention
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Suicidal Ideation focused on measuring Barrier reduction intervention, Suicidal ideation, Self-help, Suicide prevention helpline, Randomised controlled trial, Help-seeking

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Exclusion Criteria:

  • participant is younger than 16 years old.
  • participant scores below the cut-off point for severe suicidal thoughts (SIDAS score < 21).
  • participant scores above the cut-off point for severe suicidal thoughts (SIDAS score ≥ 21) and reports being likely to contact the suicide prevention helpline. They will be directly transferred to the contact details of the helpline.

Sites / Locations

  • 113 Suicide Prevention

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Intervention

Care as usual

Arm Description

After selecting a barrier in the barrier survey, participants receive tailored information with the purpose of addressing common concerns and misconceptions about the helpline.

Plain advisory text

Outcomes

Primary Outcome Measures

The use of a direct link to the helpline
The primary outcome measure is the use of a direct link to the helpline after completing the intervention or the control condition (plain advisory text, care as usual).

Secondary Outcome Measures

Self-reported likelihood of contacting the helpline
Due to the anonymous nature of the helpline, it is not possible to measure if people who do not directly use the link to the helpline, contact the helpline at a later point in time. Therefore, the self-reported likelihood of contacting the helpline (5-point interval scale, ranging from not likely to very likely) is included as a proxy measurement.

Full Information

First Posted
July 12, 2022
Last Updated
July 12, 2023
Sponsor
113 Suicide Prevention
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1. Study Identification

Unique Protocol Identification Number
NCT05458830
Brief Title
Breaking Down Barriers to a Suicide Prevention Helpline
Official Title
Breaking Down Barriers to a Suicide Prevention Helpline: a Web-based Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
October 7, 2022 (Actual)
Primary Completion Date
December 5, 2022 (Actual)
Study Completion Date
April 1, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
113 Suicide Prevention

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Every month, around four thousand people fill in the anonymous self-test for suicidal thoughts on the website of the Dutch suicide prevention helpline 113 Suicide Prevention. The self-test includes the Suicidal Ideation Attributes Scale (SIDAS) and informs people about the severity of their suicidal thoughts. The vast majority (70%) of people who complete the test score higher than the cut-off point (≥ 21) for severe suicidal thoughts. Despite this, only around 10% of test-takers navigate to the webpage about contacting the helpline. In this study the investigators test an intervention that aims to reduce barriers to contacting the helpline via chat or phone. People with severe suicidal thoughts and little motivation to contact the helpline will be randomly allocated either to a brief Barrier Reduction Intervention (BRI) or care as usual, a plain advisory text. The aim of our study is two-fold: (i) to measure the effectiveness of a brief barrier reduction intervention (BRI) in the self-test motivating people with severe suicidal thoughts to contact the helpline, and (ii) to specifically evaluate the effectiveness of the intervention in increasing service utilisation by high-risk groups for suicide such as men and people of middle age.
Detailed Description
Research suggests that people with suicidal thoughts often do not seek help, making them invisible for preventive measures and targeted support. Anonymous online help can be a low-threshold first step towards professional face-to-face help. In the Netherlands, the suicide prevention organisation '113 Suicide Prevention' provides around-the-clock anonymous support by phone and chat, as well as an online self-help course, self-assessment tests and brief online coaching and therapy. Apart from the homepage, the 'test yourself' page is the most visited section of the helpline's website. Every month, more than 4,000 people fill in the anonymous self-test for suicidal thoughts. This self-test includes the Suicidal Ideation Attributes Scale (SIDAS) and informs the test-taker of the severity of their suicidal thoughts. Although the vast majority of people who complete the test score higher than the cut-off point for severe suicidal thoughts, only approximately 10% of test-takers go on to navigate to the web-page about contacting the helpline. And although due to the anonymity of the helpline's services it is not possible to know if people follow up the advice of contacting the helpline, the difference in demographic distributions between the users of the self-test and the crisis helpline confirms the assumption that a substantial group does not continue using helpline service. While the percentage of men among the self-test users is 40%, it is only around 25% among the users of the helpline. The study is designed as a randomised controlled trial for the anonymous users of an online self-test for suicidal thoughts in which individuals with severe suicidal thoughts and no interest in contacting the helpline will be randomly allocated either to a short barrier reduction intervention (BRI) or receive a general advisory text (care as usual). To minimise the burden on our high-risk and sensitive study population, the investigators aim that it is feasible for the participants to complete the intervention within 10 minutes. The aim of our study is two-fold: (i) to measure the effectiveness of a brief barrier reduction intervention (BRI) in the self-test motivating people with severe suicidal thoughts to contact the helpline, and (ii) to specifically evaluate the effectiveness of the intervention in increasing service utilisation by high-risk groups for suicide such as men and people of middle age.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Suicidal Ideation
Keywords
Barrier reduction intervention, Suicidal ideation, Self-help, Suicide prevention helpline, Randomised controlled trial, Help-seeking

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study is designed as a randomised controlled trial for the anonymous users of an online self-test for suicidal thoughts in which individuals with severe suicidal thoughts and no interest in contacting the helpline will be randomly allocated either to a short barrier reduction intervention (BRI) or receive a general advisory text (care as usual). To minimise the burden on the high-risk and sensitive study population, the investigators aim that it is feasible to complete the intervention within 10 minutes.
Masking
Participant
Allocation
Randomized
Enrollment
775 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
After selecting a barrier in the barrier survey, participants receive tailored information with the purpose of addressing common concerns and misconceptions about the helpline.
Arm Title
Care as usual
Arm Type
Other
Arm Description
Plain advisory text
Intervention Type
Behavioral
Intervention Name(s)
Brief Barrier Reduction Intervention
Intervention Description
After selecting a barrier in the barrier survey, participants receive tailored information with the purpose of addressing common concerns and misconceptions about the helpline.
Intervention Type
Behavioral
Intervention Name(s)
Plain advisory text
Other Intervention Name(s)
care as usual
Intervention Description
Care as usual
Primary Outcome Measure Information:
Title
The use of a direct link to the helpline
Description
The primary outcome measure is the use of a direct link to the helpline after completing the intervention or the control condition (plain advisory text, care as usual).
Time Frame
immediately after intervention
Secondary Outcome Measure Information:
Title
Self-reported likelihood of contacting the helpline
Description
Due to the anonymous nature of the helpline, it is not possible to measure if people who do not directly use the link to the helpline, contact the helpline at a later point in time. Therefore, the self-reported likelihood of contacting the helpline (5-point interval scale, ranging from not likely to very likely) is included as a proxy measurement.
Time Frame
immediately after intervention
Other Pre-specified Outcome Measures:
Title
Severity of suicidal thoughts: Suicidal Ideation Attributes Scale (SIDAS)
Description
Score on the Suicidal Ideation Attributes Scale (SIDAS). The SIDAS consists of five items on a 10-point scale measuring the frequency of suicidal thoughts, controllability, closeness to attempt, distress and interference with daily activities. Total scores range from 0 to 50, with higher scores indicating more severe suicidal thoughts.
Time Frame
Baseline measurement
Title
Gender
Description
Self-reported gender identity (male/female/other)
Time Frame
Baseline measurement
Title
Age group
Description
Self-reported age group
Time Frame
Baseline measurement
Title
Receiving treatment for mental health problems
Description
Currently receiving treatment for mental health problems (yes/no/on waiting list)
Time Frame
Baseline measurement
Title
Satisfaction with the self-test
Description
Respondents' satisfaction with the self-test (intervention or control condition). 4 point-scale ranging from poor to excellent with higher scores indicating a better outcome.
Time Frame
immediately after intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Exclusion Criteria: participant is younger than 16 years old. participant scores below the cut-off point for severe suicidal thoughts (SIDAS score < 21). participant scores above the cut-off point for severe suicidal thoughts (SIDAS score ≥ 21) and reports being likely to contact the suicide prevention helpline. They will be directly transferred to the contact details of the helpline.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Saskia Mérelle
Organizational Affiliation
113 Suicide Prevention
Official's Role
Principal Investigator
Facility Information:
Facility Name
113 Suicide Prevention
City
Amsterdam
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
The data will be made available upon request

Learn more about this trial

Breaking Down Barriers to a Suicide Prevention Helpline

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