Skip to content

ACCeptation and Qualitative Evaluation of Phone-delivered Intervention

ACCeptation and Qualitative Evaluation of Phone-delivered Intervention To Prevent Suicide Reattempt

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02949453
Acronym
ACCEPT-S
Enrollment
19
Registered
2016-10-31
Start date
2017-03-03
Completion date
2019-04-04
Last updated
2019-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicide

Keywords

suicide, prevention

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.

Interventions

BEHAVIORALSemi-directed interview performed by a social sciences researcher

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

Sponsors

Hospices Civils de Lyon
CollaboratorOTHER
Hôpital le Vinatier
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Acceptation of a telephone-delivered intervention after deliberate self-harm(DSH)change from baseline after the telephone interventionanalyze the acceptability for suicidal patients in the reiteration of the suicide prevention procedure performed by telephone Callback

Secondary

MeasureTime frameDescription
Impact of telephone-delivered intervention after a deliberate self-harm (DSH)2 yearsthrough the evaluation of this device Callback, we will identify its impact on pipelines and post-crisis experiences

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026