ACCeptation and Qualitative Evaluation of Phone-delivered Intervention

Suicide Clinical Trial

— ACCEPT-S  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02949453
• Other study ID #: 2016-A00919-42
• Status: Completed
• Phase: N/A
• Start date: March 3, 2017
• Est. completion date: April 4, 2019

Study information

• Verified date: April 2018
• Source: Hôpital le Vinatier
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 19
• Est. completion date: April 4, 2019
• Est. primary completion date: April 4, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

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

Related Conditions & MeSH terms

• Suicide

Intervention

Behavioral:
• Semi-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

Locations

Country	Name	City	State
France	Hopital Vinatier	Bron

Sponsors (2)

Lead Sponsor	Collaborator
Hôpital le Vinatier	Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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	change from baseline after the telephone intervention
Secondary	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	2 years