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The (Cost-) Effectiveness of Mindfulness-training and Cognitive Behavioural Therapy in Adolescents and Young Adults With Deliberate Self Harm

The (Cost-) Effectiveness of Mindfulness-training and Cognitive Behavioural Therapy in Adolescents and Young Adults With Deliberate Self Harm

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00694668
Acronym
DSH
Enrollment
84
Registered
2008-06-10
Start date
2008-05-31
Completion date
2012-10-31
Last updated
2009-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Self-Injurious Behavior

Keywords

Deliberate Self-Harm, Self-Injurious Behaviour, Suicidal Behaviour, Cognitive behavioural therapy, Mindfulness Based cognitive therapy

Brief summary

Background: In recent years, there has been a marked rise in the frequency of young people engaging in Deliberate Self-Harm (DSH). DSH refers to all kinds of self-harming behaviour, with and without suicidal intent. Early identification and treatment of persons who engaged in DSH is important because every episode of DSH increases the risk of future episodes and, eventually, suicide. A number of comprehensive treatment programs have been developed and proven to be effective in reducing DSH in adults. Especially the modification of inadequate emotion regulation strategies seems to be essential in the prevention of future episodes of DSH. The first short-term results of a Dutch time-limited and structured individual cognitive-behavioral treatment (CBT) for DSH in adolescents and young adults also showed positive effects on repetition of DSH and associated problems. Objective: To study the effects and costs of the total individual CBT package and one of the components of the total CBT treatment package (i.e. mindfulness training) in a group format compared to Treatment-as-Usual (TAU) on the short and long term. Design: Multi-center randomized controlled clinical trial with repeated measurements at baseline (M0),and posttreatment (M6)), 12 (M12) and 18 months (M18) after baseline. Procedure: Young persons aged 15-35 who recently have engaged in DSH and have been referred to the Leiden University Medical Centre, the mental health centre Rivierduinen or the University Medical Centre St. Radboud following an act of DSH will be invited to participate. Persons reporting severe psychiatric disorders requiring intensive inpatient treatment or serious cognitive impairments will be excluded. Interventions: Participants are randomly allocated to CBT, Mindfulness-Based Cognitive Therapy(MBCT) or Treatment-as-Usual (TAU). The CBT treatment consists of up to 12 weekly sessions of individual treatment mainly consisting of emotion regulations skills, cognitive restructuring, and behavioural skills training. The MBCT training consists of 8 2-hour sessions in a group format within a three months time frame. Outcome measures: The same outcome measures to assess the clinical effects of treatment as in the previous study will be used (repetition of DSH, depression (BDI-II), anxiety (SCL-90), self-concept(RSC-Q), and suicide cognitions (SCS)) allowing a historical comparison of treatment effectiveness across both randomized clinical trials. In addition at all assessments health-related quality of life, use of medical resources and loss of productivity will be assessed (EuroQol, VAS and TTO). In addition,problems in emotion regulation (an important risk mechanism for repetition of DSH) will be assessed before and after treatment. Economic evaluation: Differences in societal costs (intervention, other (health) care and productivity)will be compared to differences in the frequency of DSH and quality adjusted life years (EuroQol, VAS and TTO). Data-analysis/power: Based on our previous study at least a medium effect of treatment on repetition of DSH may be expected. Assuming a medium effect of one of the treatments compared to TAU (delta =.75) and an attrition rate of about 20 %, at least 42 patients per study arm are needed to detect a minimal clinical relevant difference in repetition of DSH with a power of 80% and alpha set at .05.

Interventions

Brief cognitive behavioral therapy (12 sessions)

BEHAVIORALMindfulness based cognitive therapy

9 sessions MBCT in a group-format (up to 8 persons)

Sponsors

ZonMw: The Netherlands Organisation for Health Research and Development
CollaboratorOTHER
University Medical Centre Nijmegen(departement of psychiatry)
CollaboratorUNKNOWN
Leiden University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
15 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Recently engaged in an act of DSH including overdose of medication, ingestion of chemical substances and self-inflicted injuries according to the definition which is used in the WHO/Euro Multicentre Study on parasuicide:An act with non-fatal outcome in which an individual deliberately initiates a non-habitual behavior, that without intervention from other will cause self-harm, or deliberately ingests a substance in excess of the prescribed or generally recognized dosage, and which is aimed at realizing changes that the person desires via the actual or expected physical consequences(Platt et al., 1992). * Aged between 15 and 35 * Living in the region of Leiden or Nijmegen

Exclusion criteria

* Severe psychiatric disorder or substance abuse requiring intensive inpatient treatment * Serious cognitive impairments * Not be able to converse in Dutch

Design outcomes

Primary

MeasureTime frame
Repetition of DSH, measured by the suicide attempt and self injury interview (SASII). Frequency, method and other characteristics of deliberate self-harm and suicide attempts are assessed.M0, M6, M12, M18

Secondary

MeasureTime frame
Anxiety, as measured by the symptom checklist '90M0, M6, M12, M18
Hostility, as measured by the symptom checklist '90M0, M6, M12, M18
Self-concept, as measured by the Robson self-concept questionnaireM0, M6, M12, M18
Suicidal cognitions, as measured by the suicidal cognitions scaleM0, M6, M12, M18
QALYs, assessed by the EQ5DM0, M6, M12, M18
COSTS, assessed by a 6-monthly diaryM0 - M6, M6 - M12, M12 - M18
Problem-solving skills, as measured by the Means Ends Problem-Solving TestM0, M6
depression, as measured by the Beck depression Inventory IIM0, M6, M12, M18
difficulties in emotion-regulation, as measured by the difficulties in emotion regulation scaleM0, M6
general tendency to ruminate, as measured by the Ruminative Response ScaleM0, M6
mindfulness skills, as measured by the Five Facet Mindfulness QuestionnaireM0, M6
pathological dissociation, as measured by the dissociative experiences scale - taxonM0, M6
Autobiographical memory, assessed by the autobiographical memory taskM0, M6
worrying, as measured by the Penn State Worry QuestionnaireM0 M6
Experimental avoidance, as measured by the Acceptance and Action QuestionnaireM0, M6

Countries

Netherlands

Contacts

Primary ContactSuzanne de Klerk, MSc.
SKlerk@fsw.leidenuniv.nl31-71-527-3995
Backup ContactAnne van Giezen, Dr.
Giezen@fsw.leidenuniv.nl31-71-527-3729

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026