ACCeptation and Qualitative Evaluation of Phone-delivered Intervention (ACCEPT-S)
Primary Purpose
Suicide
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Semi-directed interview performed by a social sciences researcher
Sponsored by
About this trial
This is an interventional prevention trial for Suicide focused on measuring suicide, prevention
Eligibility Criteria
Inclusion Criteria:
- Deliberate self-harm in the previous week,
- 18 years old and older,
- outpatient care orientation after discharge from emergency department
Exclusion Criteria:
- Difficulties in french language,
- mental retardation
Sites / Locations
- Hopital Vinatier
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
patients after suicidal episode
Arm Description
Patients receiving a telephone-delivered intervention after deliberate self-harm (DSH)
Outcomes
Primary Outcome Measures
Acceptation of a telephone-delivered intervention after deliberate self-harm(DSH)
analyze the acceptability for suicidal patients in the reiteration of the suicide prevention procedure performed by telephone Callback
Secondary Outcome Measures
Impact of telephone-delivered intervention after a deliberate self-harm (DSH)
through the evaluation of this device Callback, we will identify its impact on pipelines and post-crisis experiences
Full Information
NCT ID
NCT02949453
First Posted
October 24, 2016
Last Updated
April 5, 2019
Sponsor
Hôpital le Vinatier
Collaborators
Hospices Civils de Lyon
1. Study Identification
Unique Protocol Identification Number
NCT02949453
Brief Title
ACCeptation and Qualitative Evaluation of Phone-delivered Intervention
Acronym
ACCEPT-S
Official Title
ACCeptation and Qualitative Evaluation of Phone-delivered Intervention To Prevent Suicide Reattempt
Study Type
Interventional
2. Study Status
Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
March 3, 2017 (Actual)
Primary Completion Date
April 4, 2019 (Actual)
Study Completion Date
April 4, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hôpital le Vinatier
Collaborators
Hospices Civils de Lyon
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
Background: Previous suicide attempt is known to be a strong risk factor for repetition and repetition is common within the first year after an episode of deliberate self-harm (DSH). There has been growing interest in brief interventions for this population that are focused on maintaining long-term contact and/or offering re-engagement with services when needed. Despite telephone-delivered interventions have shown promising results in suicide reattempt prevention, subjective impact of such brief contact interventions and effectiveness mechanisms have never been evaluated.
Detailed Description
Semi-structured in-depth interviews with 20 patients previously receiving a telephone-delivered intervention from our team. Six weeks and 3 months after a DSH, people included in telephone-delivered process will be interviewed by a social science researcher. Qualitative analysis using thematic analysis will be independently performed by two researchers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Suicide
Keywords
suicide, prevention
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
19 (Actual)
8. Arms, Groups, and Interventions
Arm Title
patients after suicidal episode
Arm Type
Experimental
Arm Description
Patients receiving a telephone-delivered intervention after deliberate self-harm (DSH)
Intervention Type
Behavioral
Intervention Name(s)
Semi-directed interview performed by a social sciences researcher
Intervention Description
Two semi-directed interviews performed by social sciences researcher:
first interview performed 6 weeks after the suicide attempt, in an suicide prevention unit, duration 1 to 1.5 hour
second interview performed 3 month after the suicide attempt, in a suicide prevention unit, duration 1 to 1.5 hour
Primary Outcome Measure Information:
Title
Acceptation of a telephone-delivered intervention after deliberate self-harm(DSH)
Description
analyze the acceptability for suicidal patients in the reiteration of the suicide prevention procedure performed by telephone Callback
Time Frame
change from baseline after the telephone intervention
Secondary Outcome Measure Information:
Title
Impact of telephone-delivered intervention after a deliberate self-harm (DSH)
Description
through the evaluation of this device Callback, we will identify its impact on pipelines and post-crisis experiences
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Deliberate self-harm in the previous week,
18 years old and older,
outpatient care orientation after discharge from emergency department
Exclusion Criteria:
Difficulties in french language,
mental retardation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
TERRA JEAN-LOUIS, PUPH
Organizational Affiliation
Centre Hospitalier le Vinatier
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hopital Vinatier
City
Bron
ZIP/Postal Code
69678
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
ACCeptation and Qualitative Evaluation of Phone-delivered Intervention
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