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(Cost)-Effectiveness of ABFT for Suicidal Youth. (REPAIR)

Primary Purpose

Suicidal Ideation

Status
Recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Attachment Based Family Therapy (ABFT) + Treatment As Usual (TAU)
Treatment As Usual (TAU)
Sponsored by
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Suicidal Ideation focused on measuring Suicidality in young adults, Attachment Based Family Therapy, (cost)-effectiveness

Eligibility Criteria

18 Years - 25 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Aged between 18 and 25. A score above 31 on the SIQ-JR (the cut-off for suicidality). Have at least one primary parent or caregiver that participates in the assessment and treatment. This could be a biological parent, stepparent, grandparent, other relative, or a foster parent. Exclusion Criteria: Other DSM-5 disorders: modest/severe substance dependency, severe conduct disorder, evidence of psychotic features or prior psychosis (assessed with the SCID-5-S). Severe cognitive impairment (e.g., mental retardation, severe developmental disorders) as evidenced by educational records, parental report and/or clinical impression. Other circumstances that might affect participation (e.g., severe medical disorder, relocation).

Sites / Locations

  • GGZ OostBrabantRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

ABFT + TAU

TAU

Arm Description

Attachment Based Family Therapy (ABFT) is a manualized treatment, that emerges from interpersonal theories that suggest suicide can be precipitated, exacerbated, or buffered against by the quality of family relationships. Parent(s)/caregiver(s) will be involved in the therapy. In the experimental group, patients will receive ABFT as an add-on therapy besides treatment as usual (TAU).

Treatment as Usual (TAU) contains all regular interventions that are currently used to treat suicidality. In the TAU group, a limited number of systemic family therapy sessions will be given (maximum 4 sessions).

Outcomes

Primary Outcome Measures

Suicidality
Suicidality is assessed by the SIQ-JR. (Reynolds & Mazza, 1999)

Secondary Outcome Measures

Suicide ideation
Assessed with the SCID-5-S, DSM 5 diagnostic interview. Michael B.First, JBWW, Lorna Smith Benjamin, Robert L. Spitzer, 2017)
Suicide attempts
Assessed with the SCID-5-S, DSM 5 diagnostic interview. Michael B.First, JBWW, Lorna Smith Benjamin, Robert L. Spitzer, 2017)
Depression (DSM 5)
Assessed with the SCID-5-S, DSM 5 diagnostic interview. Michael B.First, JBWW, Lorna Smith Benjamin, Robert L. Spitzer, 2017)
Depressive symptoms
Patient Health Questionnaire (PHQ-9).(Kroenke, Spitzer & Williams, 2001)
Parental vision on the young adults depressive symptoms
Parental vision on the young adults depression symptoms Clinical Depression Inventory second edition (CDI-2) (Bodden, Braet, & Stikkelbroek, 2016.) .
Family functioning
Self Report Measures of Family Functioning (SRFF). (Stark et al., 1990), both the young adult and the parents/caregiver
Attachment
Secure Base Script (SBS) task to asses attachment. (Waters et al., 2019; Waters & Roisman, 2019)
Health-related quality of life
Health-related quality of life: EQ-5D-5L (Versteegh et al., 2016)
Disability
World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0). (Ustun, Kostanjsek, Chatterji & Rehm, 2010)
Non-suicidal self-injury
Non-suicidal self-injury questionnaire.(Buelens, T., Luyckx, K., Kiekens, G., Gandhi, A., Muehlenkamp, J. J., & Claes, L. (2020).
Autonomy
Autonomy of the young adult, as assessed by the questionnaire. My Parents and I, a combination of items of the Emotional Autonomy Scale (EAS; Steinberg & Zilverberg, 1986) and the Psychological Separation Inventory (PSI; Hoffman 1984).
Entrapment
Entrapment Short-Form Scale (E-SF; De Beurs et al., 2020). The E-SF is a 4-item questionnaire.
Health care and associated costs and costs from productivity loss
Health care and associated costs and costs from productivity loss: TiC-P (Hakkaart-Van Roijen, 2002).

Full Information

First Posted
July 7, 2023
Last Updated
July 19, 2023
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Collaborators
KU Leuven, ZonMw: The Netherlands Organisation for Health Research and Development, Belgium Health Care Knowledge Centre
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1. Study Identification

Unique Protocol Identification Number
NCT05965622
Brief Title
(Cost)-Effectiveness of ABFT for Suicidal Youth.
Acronym
REPAIR
Official Title
Targeting Suicidality in Young Adults: a Randomized, Controlled Pragmatic, Multicentre Trial Evaluating the (Cost)-Effectiveness of Attachment Based Family Therapy Compared to Treatment as Usual
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 1, 2023 (Anticipated)
Primary Completion Date
November 15, 2025 (Anticipated)
Study Completion Date
November 14, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Collaborators
KU Leuven, ZonMw: The Netherlands Organisation for Health Research and Development, Belgium Health Care Knowledge Centre

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
Young adults who attempt to kill themselves is a common and serious mental health problem worldwide and certainly in Belgium and the Netherlands. Fatal suicide is the leading cause of death among young adults. It has devastating consequences both for the young adults themselves and for their families. It also has substantial economic costs. However, up until now, there is little research on the treatment of suicidality among young adults. The current psychological therapy approaches and drug treatments for young people at very high risk of fatal suicide attempts have only limited success. Increasing evidence indicates the importance of involving significant others in treatment and the importance of the unfulfilled need for belonging and secure attachment. The WHO recommends involving significant others in the treatment of suicidal young adults. However, in Belgium and the Netherlands, there is little knowledge on the effectiveness of family based treatments. Attachment Based Family Therapy, or ABFT, was shown to work well in several studies in the US. Also in Belgium and the Netherlands, ABFT is being used to treat suicidal young adults. However, how well it works compared to the current treatment and if it provides good value for money have not been studied in young adults. In the proposed study the investigators will test, in a real-life situation, whether ABFT works better than the current treatment and if it provides good value for money. This study is a collaboration between the Netherlands and Belgium and 6 or 7 sites will participate from each country. Sites can be hospitals, mental health centres, student health centres or private practices. Participants (138 individuals) are young adults between 18 and 25 years old who have frequent thoughts about killing themselves, and who seek mental health treatment. The investigators predict that, compared to current treatment, ABFT will reduce suicidal thoughts and suicide attempts and that this improvement will be maintained over time, and that it will be better value for money. The project will contribute to improving care for suicidal young adults with high suicide risk. Results will inform clinical guidelines and policymakers and improve the treatment of young adults with a high risk for fatal suicide, and their families.
Detailed Description
The investigators conduct a randomized controlled trial to evaluate the (cost-)effectiveness of ABFT compared to Treatment As Usual (TAU) on suicidality, as delivered in daily practice. The hypothesis is that, compared to TAU, ABFT will lead to a stronger reduction of suicidal ideation and suicidal behavior, and will be more cost-effective, will improve family functioning and young adult attachment, and that this effect will hold at follow-up. The primary objective is change in suicidality, that is, suicidal ideation, attempts and suicide as assessed by the Suicidal Ideation Questionnaire Junior (SIQ-JR), and as reported by therapists during treatment. Secondary objectives are cost-effectiveness, process, working alliance and adherence during treatment, and change in young adult depressive symptoms, family functioning, and young adult attachment. Attachment Based Family Therapy (ABFT): ABFT is a manualized treatment, that emerges from interpersonal theories that suggest suicide can be precipitated, exacerbated, or buffered against by the quality of family relationships. Therefore, ABFT focuses on strengthening parent-child attachment bonds to create a protective and secure base for young adult development. Sessions are scheduled weekly, and the intervention lasts on average 16 weeks. Treatment as usual (TAU): Participants in both arms will receive TAU, in the experimental condition ABFT will be delivered as an add-on. Most treatment centres' clinical practices rely heavily on the use of antidepressants and/or CBT or DBT. All regular interventions are allowed in TAU, except for systemic family therapy of more than 4 sessions in total. Parents are allowed to be involved in the treatment, which is part of treatment as usual, and can comprise for instance psycho-education or parental support or skill training.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Suicidal Ideation
Keywords
Suicidality in young adults, Attachment Based Family Therapy, (cost)-effectiveness

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A randomized, controlled, pragmatic, multicentre, trial in the Netherlands and Belgium with 13 participating sites.
Masking
InvestigatorOutcomes Assessor
Masking Description
Part of the research team that will collect and analyse the data are blinded.
Allocation
Randomized
Enrollment
138 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ABFT + TAU
Arm Type
Experimental
Arm Description
Attachment Based Family Therapy (ABFT) is a manualized treatment, that emerges from interpersonal theories that suggest suicide can be precipitated, exacerbated, or buffered against by the quality of family relationships. Parent(s)/caregiver(s) will be involved in the therapy. In the experimental group, patients will receive ABFT as an add-on therapy besides treatment as usual (TAU).
Arm Title
TAU
Arm Type
Placebo Comparator
Arm Description
Treatment as Usual (TAU) contains all regular interventions that are currently used to treat suicidality. In the TAU group, a limited number of systemic family therapy sessions will be given (maximum 4 sessions).
Intervention Type
Behavioral
Intervention Name(s)
Attachment Based Family Therapy (ABFT) + Treatment As Usual (TAU)
Intervention Description
Attachment Based Family Therapy (ABFT): ABFT is a manualized treatment, that emerges from interpersonal theories that suggest suicide can be precipitated, exacerbated, or buffered against by the quality of family relationships. Therefore, ABFT focuses on strengthening parent-child attachment bonds to create a protective and secure base for young adult development. Sessions are scheduled weekly, and the intervention lasts on average 16 weeks. The participants in the ABFT condition will also receive treatment as usual (TAU).
Intervention Type
Behavioral
Intervention Name(s)
Treatment As Usual (TAU)
Intervention Description
The participants in the treatment as usual (TAU) condition will only receive regular existing care to treat suicidality in young adults.
Primary Outcome Measure Information:
Title
Suicidality
Description
Suicidality is assessed by the SIQ-JR. (Reynolds & Mazza, 1999)
Time Frame
Measures change at: baseline, 5 months after baseline (immediately after intervention).Follow-up: 3-mo after intervention (i.e. 8 mo after baseline), 6 mo after intervention (i.e11-mo after baseline) 12 mo after intervention(i.e.17 mo after baseline)
Secondary Outcome Measure Information:
Title
Suicide ideation
Description
Assessed with the SCID-5-S, DSM 5 diagnostic interview. Michael B.First, JBWW, Lorna Smith Benjamin, Robert L. Spitzer, 2017)
Time Frame
Measures change at: baseline, 5 months after baseline (after intervention).Follow-up: 3-months after intervention (i.e. 8 months after baseline), 12-months after intervention (i.e. 17 months after baseline)
Title
Suicide attempts
Description
Assessed with the SCID-5-S, DSM 5 diagnostic interview. Michael B.First, JBWW, Lorna Smith Benjamin, Robert L. Spitzer, 2017)
Time Frame
Measures change at: baseline, 5 months after baseline (after intervention).Follow-up: 3-months after intervention (i.e. 8 months after baseline), 12-months after intervention (i.e. 17 months after baseline)
Title
Depression (DSM 5)
Description
Assessed with the SCID-5-S, DSM 5 diagnostic interview. Michael B.First, JBWW, Lorna Smith Benjamin, Robert L. Spitzer, 2017)
Time Frame
Measures change at: baseline, 5 months after baseline (after intervention).Follow-up: 3-months after intervention (i.e. 8 months after baseline), 12-months after intervention (i.e. 17 months after baseline)
Title
Depressive symptoms
Description
Patient Health Questionnaire (PHQ-9).(Kroenke, Spitzer & Williams, 2001)
Time Frame
Measures change at: baseline, 5 months after baseline (immediately after intervention).Follow-up: 3-mo after intervention (i.e. 8 mo after baseline), 6 mo after intervention (i.e11-mo after baseline) 12 mo after intervention(i.e.17 mo after baseline)
Title
Parental vision on the young adults depressive symptoms
Description
Parental vision on the young adults depression symptoms Clinical Depression Inventory second edition (CDI-2) (Bodden, Braet, & Stikkelbroek, 2016.) .
Time Frame
Measures change at: baseline, 5 months after baseline (immediately after intervention).Follow-up: 3-mo after intervention (i.e. 8 mo after baseline), 6 mo after intervention (i.e11-mo after baseline) 12 mo after intervention(i.e.17 mo after baseline)
Title
Family functioning
Description
Self Report Measures of Family Functioning (SRFF). (Stark et al., 1990), both the young adult and the parents/caregiver
Time Frame
Measures change at: baseline, 5 months after baseline (immediately after intervention).Follow-up: 3-mo after intervention (i.e. 8 mo after baseline), 6 mo after intervention (i.e11-mo after baseline) 12 mo after intervention(i.e.17 mo after baseline)
Title
Attachment
Description
Secure Base Script (SBS) task to asses attachment. (Waters et al., 2019; Waters & Roisman, 2019)
Time Frame
Measures change at: baseline, 5 months after baseline (immediately after intervention).Follow-up: 3-months after intervention (i.e. 8 months after baseline), 12-months after intervention (i.e. 17 months after baseline)
Title
Health-related quality of life
Description
Health-related quality of life: EQ-5D-5L (Versteegh et al., 2016)
Time Frame
Measures change at: baseline, 5 months after baseline (immediately after intervention).Follow-up: 3-months after intervention (i.e. 8 months after baseline), 12-months after intervention (i.e. 17 months after baseline)
Title
Disability
Description
World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0). (Ustun, Kostanjsek, Chatterji & Rehm, 2010)
Time Frame
Measures change at: baseline, 5 months after baseline (immediately after intervention).Follow-up: 3-months after intervention (i.e. 8 months after baseline), 12-months after intervention (i.e. 17 months after baseline)
Title
Non-suicidal self-injury
Description
Non-suicidal self-injury questionnaire.(Buelens, T., Luyckx, K., Kiekens, G., Gandhi, A., Muehlenkamp, J. J., & Claes, L. (2020).
Time Frame
Measures change at: baseline, 5 months after baseline (immediately after intervention).Follow-up: 3-mo after intervention (i.e. 8 mo after baseline), 6 mo after intervention (i.e11-mo after baseline) 12 mo after intervention(i.e.17 mo after baseline)
Title
Autonomy
Description
Autonomy of the young adult, as assessed by the questionnaire. My Parents and I, a combination of items of the Emotional Autonomy Scale (EAS; Steinberg & Zilverberg, 1986) and the Psychological Separation Inventory (PSI; Hoffman 1984).
Time Frame
Measures change at: baseline, 5 months after baseline (immediately after intervention).Follow-up: 3-mo after intervention (i.e. 8 mo after baseline), 6 mo after intervention (i.e11-mo after baseline) 12 mo after intervention(i.e.17 mo after baseline)
Title
Entrapment
Description
Entrapment Short-Form Scale (E-SF; De Beurs et al., 2020). The E-SF is a 4-item questionnaire.
Time Frame
Measures change at: baseline, 5 months after baseline (immediately after intervention).Follow-up: 3-mo after intervention (i.e. 8 mo after baseline), 6 mo after intervention (i.e11-mo after baseline) 12 mo after intervention(i.e.17 mo after baseline)
Title
Health care and associated costs and costs from productivity loss
Description
Health care and associated costs and costs from productivity loss: TiC-P (Hakkaart-Van Roijen, 2002).
Time Frame
Measures change at: baseline, 5 months after baseline (immediately after intervention).Follow-up: 3-months after intervention (i.e. 8 months after baseline), 12-months after intervention (i.e. 17 months after baseline)
Other Pre-specified Outcome Measures:
Title
Childhood Trauma
Description
Childhood Trauma Questionnaire (CTQ). This is a self-report 28-item questionnaire that measures 5 types of maltreatment: emotional, physical, and sexual abuse, and emotional and physical neglect.
Time Frame
Baseline
Title
Working Alliance Inventory
Description
Working Alliance Inventory (WAI). Measures overall therapeutic alliance and consists of sub scales measuring (quality of therapy) tasks, goals and bonds. Admistered to young adult and the participating parent or caregiver.
Time Frame
Every 2 months during intervention starting at the first session
Title
Treatment fidelity
Description
The Therapist Behavior Rating Scale-3 & non-verbal contact will be assessd via videotaping by a trained researcher.
Time Frame
Every 2 months during intervention starting at the first session
Title
Therapy Procedure
Description
Therapy Procedures Checklist (TPC). It assesses therapists' reports of the techniques they employ when working with child and adolescent clients, and will be used to monitor Treatment as Usual in both study arms. TPC items encompass the 3 most common therapeutic models for youth: psychodynamic, cognitive, and behavioural.
Time Frame
Every 2 months during intervention starting at the first session
Title
Demographic characteristics and other parameters
Description
Demographic characteristics: age, marital status, gender, ethnicity, level of education, medication use, substance use (smoking, alcohol, drugs), psychiatric history (therapy, medication, number of previous episodes, duration of episodes and treatment).
Time Frame
Baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged between 18 and 25. A score above 31 on the SIQ-JR (the cut-off for suicidality). Have at least one primary parent or caregiver that participates in the assessment and treatment. This could be a biological parent, stepparent, grandparent, other relative, or a foster parent. Exclusion Criteria: Other DSM-5 disorders: modest/severe substance dependency, severe conduct disorder, evidence of psychotic features or prior psychosis (assessed with the SCID-5-S). Severe cognitive impairment (e.g., mental retardation, severe developmental disorders) as evidenced by educational records, parental report and/or clinical impression. Other circumstances that might affect participation (e.g., severe medical disorder, relocation).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Claudi L.H. Bockting, Professor
Phone
+3120-8913600
Email
c.l.bockting@amsterdamumc.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Nadia Van Der Spek, PhD
Phone
+31624138237
Email
n.vanderspek@amsterdamumc.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nadia van der Spek, PhD
Organizational Affiliation
Academic Medical Center (AMC)
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Claudi Bockting, professor
Organizational Affiliation
Academic Medical Center (AMC)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Guy Bosmans, Professor
Organizational Affiliation
KU Leuven
Official's Role
Study Director
Facility Information:
Facility Name
GGZ OostBrabant
City
Oss
State/Province
Noord Holland
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hanneke Niels, MSc
Phone
+31634238923
Email
hanneke.niels@ggzoostbrabant.nl

12. IPD Sharing Statement

Plan to Share IPD
No

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(Cost)-Effectiveness of ABFT for Suicidal Youth.

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