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Safety Intervention for Improving Functioning in Suicidal Attempters (STRONG)

Primary Purpose

Suicide, Attempted, Functioning, Psychosocial

Status
Not yet recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Safety Intervention Planning
Sponsored by
Hospital Clinic of Barcelona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Suicide, Attempted focused on measuring suicide, cognition, neuroimaging, psychosocial functioning, quality of life

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Age over 18 years old Having attempted suicide Provide written informed consent No claustrophobia/metallic objects/implants Exclusion Criteria: Intelligence quotient below 70 and impaired functioning Any medical condition that could affect neuropsychological performance (such as neurological diseases) or a history of head trauma with loss of consciousness Participation in any structured psychological intervention within the past 6 months Patients who received electroconvulsive therapy within the past 6 months Inability to give inform consent

Sites / Locations

  • Hospital Clínic Barcelona

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Treatment As Usual

Intervention Group

Arm Description

(TAU)

Treatment As Usual + Safety Intervention Planning.

Outcomes

Primary Outcome Measures

Psychosocial functioning changes in Functioning Assessment Short Test (FAST).
Suicidal attempters receiving a safety planning intervention will show a decrease in FAST scores, compared to those suicidal attempters receiving treatment as usual. Lower general scores on this scale indicate better psychosocial functioning.

Secondary Outcome Measures

Cognitive changes in executive functions, specifically in decision-making measured by Iowa Gambling Task (IGT).
Suicidal attempters receiving a safety planning intervention will experience greater improvement in cognitive performance, particularly in decision-making compared to those suicidal attempters receiving treatment as usual. A proxy of decision-making ability is extracted by means of a formula taking into account number of safe choices minus risky selections in terms of alll choices during the task. Higher scores are related to better decision-making ability. Normative data has been published for Spanish population and will be used to assess improvement based on the baseline visit (vs. performance 6-month follow-up).
Cognitive changes in executive functions, specifically in impulsivity measured by Stroop Test (Stroop).
Suicidal attempters receiving a safety planning intervention will experience greater improvement in cognitive performance, particularly in inhibition compared to those suicidal attempters receiving treatment as usual. Inhibitory control will be assessed by measure of interference obtained through Stroop test. Higher scores here mean better inhibitory control, thus less impulsivity. Normative data are taken from the original version of Stroop Test and will be used to assess improvement based on the baseline visit (vs. performance 6-month follow-up).
Cognitive changes in executive functions, specifically in attention measured by Conners' Performance Test v.5 (CPT-II).
Suicidal attempters receiving a safety planning intervention will experience greater improvement in cognitive performance, particularly in attention, compared to those suicidal attempters receiving treatment as usual. Measures used to assess inattention include: omissions, commissions, Hit Reaction Time (RT), Detectability (d'), Hit RT Block Change and Hit RT Inter-Stimulus Intervals (ISI) Change by means of CPT-II. All measures taken together provide an index of inattention, which is based on T-scores. In this test, higher scores reflect greater impairment. Normative data has been published in CPT II V.5 and will be used to assess improvement based on the baseline visit (vs. performance 6-month follow-up).
Changes in self-reported quality of life by Quality of Life 5-Dimensions scale (EuroQoL-5D).
Suicidal attempters receiving a safety planning intervention will show greater improvement in quality of life compared to those suicidal attempters receiving treatment as usual taking into account baseline measures self-reported in comparison with the following visits. This scale comprises two subscales: First subscale measures quality of life using a descriptive system by dimensions (mobility, self-care, activities of daily living, pain/discomfort and anxiety/depression). The higher the score here, the worse the quality of life. Second subscale uses a visual analog scale from 0 to 100 for self-reporting overall quality of life. Higher scores here reflect better quality of life. All items refer to the current day.
Clinical changes in suicidal behavior assessed by the Columbia-Suicide Severity Rating Scale (C-SSRS).
Suicidal attempters receiving a safety planning intervention will not show suicidal behavior measured by C-SSRS in the two follow-up visits after intervention with Safety Planning Intervention (SPI) compared to those suicidal attempters receiving treatment as usual.
Clinical changes in depressive symptomatology assessed by Patient Health Questionnaire (PHQ-9).
Patient Health Questionnaire (PHQ-9) measures frequence of depressive symptoms occurrence. Lower scores show less depressive-related symptomatology. PHQ-9 scores following intervention are expected to be lower than at baseline.
Clinical changes in anxious symptomatology assessed by Generalized Anxiety Disorder (GAD-7).
Generalized Anxiety Disorder (GAD-7) measures frequence of anxious symptoms occurrence. Lower scores show less anxiety-related symptomatology. GAD-7 scores following intervention are expected to be lower than at baseline.
Changes in activation of different areas of the prefrontal cortex measured by functional Magnetic Resonance Imagining (fMRI).
Suicidal attempters receiving a safety planning intervention will show changes in different areas of the prefrontal cortex. Changes expected include resting and activation conditions. We expect to detect more activation in prefrontal cortex (PFC) areas such as the ventrolateral PFC (including the orbitofrontal cortex), the anterior cingulate gyrus, the dorsomedial PFC and the dorsolateral PFC in patients receiving psychological intervention (in comparison with their baseline performance in task-related fMRI). Other areas such as the amygdala and medial temporal cortex will also be explored. Additionally, alterations in white matter connections measures by Diffusion Weighted Imaging (DWI) and Diffusion Tensor Imagining (DTI) will be assessed at baseline and will be compared with 6-months follow up imaging acquisition. Moreover, possible anatomical changes in prefrontal cortex areas will be also assessed.

Full Information

First Posted
October 25, 2022
Last Updated
December 15, 2022
Sponsor
Hospital Clinic of Barcelona
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1. Study Identification

Unique Protocol Identification Number
NCT05655390
Brief Title
Safety Intervention for Improving Functioning in Suicidal Attempters
Acronym
STRONG
Official Title
Safety Intervention for Improving Functioning in Suicidal Attempters
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 2023 (Anticipated)
Primary Completion Date
February 2024 (Anticipated)
Study Completion Date
January 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Clinic of Barcelona

4. Oversight

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

5. Study Description

Brief Summary
The goal of this clinical trial is to assess the effectiveness of a safety planning intervention in suicidal attempters by improving their psychosocial functional outcome and therefore enhancing their ability to perform the activities of daily living. As secondary objectives, assessment of the effectiveness of a safety planning intervention in suicidal attempters will be performed by determining cognitive performance (particularly decision-making, inhibition and attention), quality of life, clinical state and relating all these data with neuroimaging correlates. Target neuroimaging areas will be the orbitofrontal cortex and dorsal prefrontal cortex.
Detailed Description
Design: STRONG is a single-centre experimental randomized clinical trial for suicidal attempters involving a safety planning intervention and 3- to 6-months follow-ups. This study will be carried out in the Bipolar and Depressive Disorders Unit, at Hospital Clínic de Barcelona. It will be rater-blinded and will include two parallel arms (1:1) in order to assess the efficacy of a safety planning intervention compared with treatment as usual. This project has been approved by the Ethical Committee of the Hospital Clinic of Barcelona and it will be carried up in accordance with the ethical principles of the Declaration of Helsinki and Good Clinical Practice in compliance with the data protection law in force and anonymization of the collected information. Procedures: Subsequent to signing the informed consent, a complete baseline evaluation will be carried out which includes acquisition of socio-demographic and clinical variables, psychosocial functioning, cognitive performance, quality of life assessment and neuroimaging determinations (v0). Thereafter, the whole sample will be randomized in two groups of 60 participants by parallel assignment. A group of 60 people will exclusively receive treatment as usual (non-intervention group); whereas the other group of 60 participants will receive a safety planning intervention in addition to their treatment as usual (experimental group). After two months of finishing the intervention of 4 weeks (or three months after baseline), suicidal attempters will be reassessed from a socio-demographic, clinical, psychosocial functioning, quality of life assessment as well as brief neuropsychological evaluation (v1). The neuropsychological assessment in this point will be shorter to avoid learning effect. Five months after intervention (or 6-months after baseline), a completely socio-demographic, clinical psychosocial functioning, quality of life assessment as well as neuropsychological and neuroimaging evaluation will be carried out (v2). Assessments: A) Socio-demographic variables: Information on gender, age, marital status, current type of cohabitation, number of offspring (if any), educational level, years of education, employment status and socioeconomic status. B) Clinical, psychosocial functioning, quality of life evaluation: Suicidal ideation and behaviour, clinical symptomatology, in general and depressive symptoms and anxiety symptoms in particular, lifetime history of psychiatric or medical comorbidities, diagnosis, number of hospitalizations, family history of affective and psychiatric disorders, and pharmacological treatment will be collected for all subjects, premorbid adjustment, psychosocial functioning, quality of life, impulsiveness, reflective functioning and stress associated with life events will be also assessed using standardized questionnaires. Clinical variables will be assessed at baseline, two months post-intervention and at the 6-month follow-up. C) Neuropsychological assessment: Intelligence quotient, attention, processing speed, verbal and visual memory, working memory, and executive functions will be assessed in all subjects. The extended neuropsychological battery will be administered at baseline and at 6 months. To avoid learning effects, only some of the tests evaluating attention and executive functions will be administered in the 2-month assessment post-intervention. D) Neuroimaging assessment: Magnetic resonance imaging (MRI) will be performed at baseline, and in the 6-month follow-up. Data acquisition will be performed using a full-body MRI scanner, a Siemens Magnetom Prisma 3 Teslas. A part from structural T1, resting-state functional MRI, and diffusion-weighted imaging, two tasks related to decision making and inhibition will be carried out. Non-contrast MRI will be used. Participants will not be exposed to radiation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Suicide, Attempted, Functioning, Psychosocial
Keywords
suicide, cognition, neuroimaging, psychosocial functioning, quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Experimental randomized clinical study. Rater-blinded. Sample: Suicidal attempters.
Masking
Investigator
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Treatment As Usual
Arm Type
No Intervention
Arm Description
(TAU)
Arm Title
Intervention Group
Arm Type
Experimental
Arm Description
Treatment As Usual + Safety Intervention Planning.
Intervention Type
Behavioral
Intervention Name(s)
Safety Intervention Planning
Intervention Description
The therapy is based on the iFightDepression platform implemented by the European Alliance against Depression. The aim of this specific therapy is to help individuals to acquire strategies to regulate emotions and learn to tolerate discomfort preventing the imminent risk for suicidal behavior. The safety planning intervention will be conducted by identifying warning signs and provide each individual with personal and individualized coping strategies and sources of support. Main skills to be acquired and integrated for the individual are as it follows: 1) Contingency plan by five steps (identification of warning signs; applying internal coping strategies; network as distraction; safe environment; reasons for living and contact professionals), 2) Mindfulness, 3) Discomfort tolerance, and 4) Regulating emotions.
Primary Outcome Measure Information:
Title
Psychosocial functioning changes in Functioning Assessment Short Test (FAST).
Description
Suicidal attempters receiving a safety planning intervention will show a decrease in FAST scores, compared to those suicidal attempters receiving treatment as usual. Lower general scores on this scale indicate better psychosocial functioning.
Time Frame
2 months after intervention; 5 months after intervention
Secondary Outcome Measure Information:
Title
Cognitive changes in executive functions, specifically in decision-making measured by Iowa Gambling Task (IGT).
Description
Suicidal attempters receiving a safety planning intervention will experience greater improvement in cognitive performance, particularly in decision-making compared to those suicidal attempters receiving treatment as usual. A proxy of decision-making ability is extracted by means of a formula taking into account number of safe choices minus risky selections in terms of alll choices during the task. Higher scores are related to better decision-making ability. Normative data has been published for Spanish population and will be used to assess improvement based on the baseline visit (vs. performance 6-month follow-up).
Time Frame
2 months after intervention; 5 months after intervention
Title
Cognitive changes in executive functions, specifically in impulsivity measured by Stroop Test (Stroop).
Description
Suicidal attempters receiving a safety planning intervention will experience greater improvement in cognitive performance, particularly in inhibition compared to those suicidal attempters receiving treatment as usual. Inhibitory control will be assessed by measure of interference obtained through Stroop test. Higher scores here mean better inhibitory control, thus less impulsivity. Normative data are taken from the original version of Stroop Test and will be used to assess improvement based on the baseline visit (vs. performance 6-month follow-up).
Time Frame
2 months after intervention; 5 months after intervention
Title
Cognitive changes in executive functions, specifically in attention measured by Conners' Performance Test v.5 (CPT-II).
Description
Suicidal attempters receiving a safety planning intervention will experience greater improvement in cognitive performance, particularly in attention, compared to those suicidal attempters receiving treatment as usual. Measures used to assess inattention include: omissions, commissions, Hit Reaction Time (RT), Detectability (d'), Hit RT Block Change and Hit RT Inter-Stimulus Intervals (ISI) Change by means of CPT-II. All measures taken together provide an index of inattention, which is based on T-scores. In this test, higher scores reflect greater impairment. Normative data has been published in CPT II V.5 and will be used to assess improvement based on the baseline visit (vs. performance 6-month follow-up).
Time Frame
2 months after intervention; 5 months after intervention
Title
Changes in self-reported quality of life by Quality of Life 5-Dimensions scale (EuroQoL-5D).
Description
Suicidal attempters receiving a safety planning intervention will show greater improvement in quality of life compared to those suicidal attempters receiving treatment as usual taking into account baseline measures self-reported in comparison with the following visits. This scale comprises two subscales: First subscale measures quality of life using a descriptive system by dimensions (mobility, self-care, activities of daily living, pain/discomfort and anxiety/depression). The higher the score here, the worse the quality of life. Second subscale uses a visual analog scale from 0 to 100 for self-reporting overall quality of life. Higher scores here reflect better quality of life. All items refer to the current day.
Time Frame
2 months after intervention; 5 months after intervention
Title
Clinical changes in suicidal behavior assessed by the Columbia-Suicide Severity Rating Scale (C-SSRS).
Description
Suicidal attempters receiving a safety planning intervention will not show suicidal behavior measured by C-SSRS in the two follow-up visits after intervention with Safety Planning Intervention (SPI) compared to those suicidal attempters receiving treatment as usual.
Time Frame
2 months after intervention; 5 months after intervention
Title
Clinical changes in depressive symptomatology assessed by Patient Health Questionnaire (PHQ-9).
Description
Patient Health Questionnaire (PHQ-9) measures frequence of depressive symptoms occurrence. Lower scores show less depressive-related symptomatology. PHQ-9 scores following intervention are expected to be lower than at baseline.
Time Frame
2 months after intervention; 5 months after intervention
Title
Clinical changes in anxious symptomatology assessed by Generalized Anxiety Disorder (GAD-7).
Description
Generalized Anxiety Disorder (GAD-7) measures frequence of anxious symptoms occurrence. Lower scores show less anxiety-related symptomatology. GAD-7 scores following intervention are expected to be lower than at baseline.
Time Frame
2 months after intervention; 5 months after intervention
Title
Changes in activation of different areas of the prefrontal cortex measured by functional Magnetic Resonance Imagining (fMRI).
Description
Suicidal attempters receiving a safety planning intervention will show changes in different areas of the prefrontal cortex. Changes expected include resting and activation conditions. We expect to detect more activation in prefrontal cortex (PFC) areas such as the ventrolateral PFC (including the orbitofrontal cortex), the anterior cingulate gyrus, the dorsomedial PFC and the dorsolateral PFC in patients receiving psychological intervention (in comparison with their baseline performance in task-related fMRI). Other areas such as the amygdala and medial temporal cortex will also be explored. Additionally, alterations in white matter connections measures by Diffusion Weighted Imaging (DWI) and Diffusion Tensor Imagining (DTI) will be assessed at baseline and will be compared with 6-months follow up imaging acquisition. Moreover, possible anatomical changes in prefrontal cortex areas will be also assessed.
Time Frame
5 months after intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age over 18 years old Having attempted suicide Provide written informed consent No claustrophobia/metallic objects/implants Exclusion Criteria: Intelligence quotient below 70 and impaired functioning Any medical condition that could affect neuropsychological performance (such as neurological diseases) or a history of head trauma with loss of consciousness Participation in any structured psychological intervention within the past 6 months Patients who received electroconvulsive therapy within the past 6 months Inability to give inform consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Iria Grande
Phone
+34932275400
Ext
3130
Email
igrande@clinic.cat
First Name & Middle Initial & Last Name or Official Title & Degree
Natalia Roberto
Phone
+34932275400
Ext
4389
Email
roberto@recerca.clinic.cat
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Iria Grande
Organizational Affiliation
IDIBAPS- Hospital Clinic de Barcelona
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Clínic Barcelona
City
Barcelona
ZIP/Postal Code
08036
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data will be shared only under a justified request. Names and personal data will never be displayed or shared with third parties. The data will be collected in an information file owned by the center. The research team undertakes to preserve the privacy of patients and the confidentiality of data, in accordance with the Organic Law 3/2018, 5th December, about Personal Data Protection. In case of transfer of data to third parties (external promoter to the center) these will be transferred in an encrypted system, eliminating any data that could identify the patient. Only the principal investigator and her team will have access to the list of patient identification codes.
IPD Sharing Time Frame
When approved by the PI. For a period of 6 months at maximum.
IPD Sharing Access Criteria
Only coded data will be transferred to third parties and to other countries, which in no case will contain information that can directly identify the participant (such as name and surname, initials, address, social security number, etc.). In the event of such a transfer, it would be for the same purpose of the study described above and guaranteeing confidentiality.

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Safety Intervention for Improving Functioning in Suicidal Attempters

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