- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02949453
ACCeptation and Qualitative Evaluation of Phone-delivered Intervention (ACCEPT-S)
April 5, 2019 updated by: Hôpital le Vinatier
ACCeptation and Qualitative Evaluation of Phone-delivered Intervention To Prevent Suicide Reattempt
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
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.
Study Type
Interventional
Enrollment (Actual)
19
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Bron, France, 69678
- Hopital Vinatier
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: patients after suicidal episode
Patients receiving a telephone-delivered intervention after deliberate self-harm (DSH)
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Two semi-directed interviews performed by social sciences researcher:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Acceptation of a telephone-delivered intervention after deliberate self-harm(DSH)
Time Frame: change from baseline after the telephone intervention
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analyze the acceptability for suicidal patients in the reiteration of the suicide prevention procedure performed by telephone Callback
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change from baseline after the telephone intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Impact of telephone-delivered intervention after a deliberate self-harm (DSH)
Time Frame: 2 years
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through the evaluation of this device Callback, we will identify its impact on pipelines and post-crisis experiences
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: TERRA JEAN-LOUIS, PUPH, Centre Hospitalier Le Vinatier
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 3, 2017
Primary Completion (Actual)
April 4, 2019
Study Completion (Actual)
April 4, 2019
Study Registration Dates
First Submitted
October 24, 2016
First Submitted That Met QC Criteria
October 27, 2016
First Posted (Estimate)
October 31, 2016
Study Record Updates
Last Update Posted (Actual)
April 8, 2019
Last Update Submitted That Met QC Criteria
April 5, 2019
Last Verified
April 1, 2018
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2016-A00919-42
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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