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Clinical Trials in Belgium / NCT05965622
Recruiting Not applicable

(Cost)-Effectiveness of ABFT for Suicidal Youth.

NCT05965622 · tracked via the Priya Life Science Belgium tracker
Phase
Not applicable
Started
2023-10-05
Last updated
2024-08-22

Condition(s) studied

Suicidal Ideation

Investigational drug(s) / intervention(s)

Attachment Based Family Therapy (ABFT) + Treatment As Usual (TAU)Treatment As Usual (TAU)

Attachment Based Family Therapy (ABFT) + Treatment As Usual (TAU): 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).

Treatment As Usual (TAU): The participants in the treatment as usual (TAU) condition will only receive regular existing care to treat suicidality in young adults.

Study 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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
25 Years
Healthy volunteers
No
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: substance dependency: severe alcohol or cannabis use disorder, all other substances: modest or severe substance use disorder. * 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).

Primary outcome measure(s)

Trial sites (13)

FacilityCityRegionStatus
Prakijkt ConnectUs Tongeren Limburg Recruiting
UGent Centrum Kind en Adolescent Ghent Oost-Vlaanderen Not Yet Recruiting
UPC KU Leuven, campus Kortenberg Kortenberg Vlaams-Brabant Recruiting
PraxisP Leuven Vlaams-Brabant Not Yet Recruiting
STUVO Psychologen en Psychiaters Leuven Vlaams-Brabant Recruiting
Praktijk Annemie Uyttersprot Merchtem Vlaams-Brabant Recruiting
GGzE Eindhoven North Brabant Recruiting
GGZ Oost Brabant Oss North Brabant Recruiting
Academisch Medisch Centrum Amsterdam North Holland Not Yet Recruiting
Arkin Amsterdam North Holland Recruiting
Levvel Amsterdam North Holland Not Yet Recruiting
Kenter Jeugdhulp Santpoort-Noord North Holland Recruiting
GGz Centraal Amersfoort Utrecht Recruiting

More Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) trials in Belgium

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05965622 on ClinicalTrials.gov ↗ ← All trials in Belgium