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

Primary Purpose

Self-Injurious Behavior

Status
Unknown status
Phase
Phase 2
Locations
Netherlands
Study Type
Interventional
Intervention
Cognitive Behavioral treatment
Mindfulness based cognitive therapy
Sponsored by
Leiden University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Self-Injurious Behavior focused on measuring Deliberate Self-Harm, Self-Injurious Behaviour, Suicidal Behaviour, Cognitive behavioural therapy, Mindfulness Based cognitive therapy

Eligibility Criteria

15 Years - 35 Years (Child, Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • University Medical Centre St. RadboudRecruiting
  • Leiden University Medical CentreRecruiting
  • Rivierduinen Mental Health CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

1

2

Arm Description

Cognitive Behavioural Treatment

Mindfulness Based Cognitive Therapy-training

Outcomes

Primary Outcome Measures

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.

Secondary Outcome Measures

depression, as measured by the Beck depression Inventory II
Anxiety, as measured by the symptom checklist '90
Hostility, as measured by the symptom checklist '90
Self-concept, as measured by the Robson self-concept questionnaire
Suicidal cognitions, as measured by the suicidal cognitions scale
QALYs, assessed by the EQ5D
COSTS, assessed by a 6-monthly diary
Problem-solving skills, as measured by the Means Ends Problem-Solving Test
Experimental avoidance, as measured by the Acceptance and Action Questionnaire
difficulties in emotion-regulation, as measured by the difficulties in emotion regulation scale
general tendency to ruminate, as measured by the Ruminative Response Scale
mindfulness skills, as measured by the Five Facet Mindfulness Questionnaire
pathological dissociation, as measured by the dissociative experiences scale - taxon
Autobiographical memory, assessed by the autobiographical memory task
worrying, as measured by the Penn State Worry Questionnaire

Full Information

First Posted
June 5, 2008
Last Updated
November 5, 2009
Sponsor
Leiden University Medical Center
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development, University Medical Centre Nijmegen(departement of psychiatry)
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1. Study Identification

Unique Protocol Identification Number
NCT00694668
Brief Title
The (Cost-) Effectiveness of Mindfulness-training and Cognitive Behavioural Therapy in Adolescents and Young Adults With Deliberate Self Harm
Acronym
DSH
Official Title
The (Cost-) Effectiveness of Mindfulness-training and Cognitive Behavioural Therapy in Adolescents and Young Adults With Deliberate Self Harm
Study Type
Interventional

2. Study Status

Record Verification Date
November 2009
Overall Recruitment Status
Unknown status
Study Start Date
May 2008 (undefined)
Primary Completion Date
November 2010 (Anticipated)
Study Completion Date
October 2012 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Leiden University Medical Center
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development, University Medical Centre Nijmegen(departement of psychiatry)

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Self-Injurious Behavior
Keywords
Deliberate Self-Harm, Self-Injurious Behaviour, Suicidal Behaviour, Cognitive behavioural therapy, Mindfulness Based cognitive therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
84 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Cognitive Behavioural Treatment
Arm Title
2
Arm Type
Experimental
Arm Description
Mindfulness Based Cognitive Therapy-training
Intervention Type
Behavioral
Intervention Name(s)
Cognitive Behavioral treatment
Intervention Description
Brief cognitive behavioral therapy (12 sessions)
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness based cognitive therapy
Intervention Description
9 sessions MBCT in a group-format (up to 8 persons)
Primary Outcome Measure Information:
Title
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.
Time Frame
M0, M6, M12, M18
Secondary Outcome Measure Information:
Title
depression, as measured by the Beck depression Inventory II
Time Frame
M0, M6, M12, M18
Title
Anxiety, as measured by the symptom checklist '90
Time Frame
M0, M6, M12, M18
Title
Hostility, as measured by the symptom checklist '90
Time Frame
M0, M6, M12, M18
Title
Self-concept, as measured by the Robson self-concept questionnaire
Time Frame
M0, M6, M12, M18
Title
Suicidal cognitions, as measured by the suicidal cognitions scale
Time Frame
M0, M6, M12, M18
Title
QALYs, assessed by the EQ5D
Time Frame
M0, M6, M12, M18
Title
COSTS, assessed by a 6-monthly diary
Time Frame
M0 - M6, M6 - M12, M12 - M18
Title
Problem-solving skills, as measured by the Means Ends Problem-Solving Test
Time Frame
M0, M6
Title
Experimental avoidance, as measured by the Acceptance and Action Questionnaire
Time Frame
M0, M6
Title
difficulties in emotion-regulation, as measured by the difficulties in emotion regulation scale
Time Frame
M0, M6
Title
general tendency to ruminate, as measured by the Ruminative Response Scale
Time Frame
M0, M6
Title
mindfulness skills, as measured by the Five Facet Mindfulness Questionnaire
Time Frame
M0, M6
Title
pathological dissociation, as measured by the dissociative experiences scale - taxon
Time Frame
M0, M6
Title
Autobiographical memory, assessed by the autobiographical memory task
Time Frame
M0, M6
Title
worrying, as measured by the Penn State Worry Questionnaire
Time Frame
M0 M6

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Suzanne de Klerk, MSc.
Phone
31-71-527-3995
Email
SKlerk@fsw.leidenuniv.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Anne van Giezen, Dr.
Phone
31-71-527-3729
Email
Giezen@fsw.leidenuniv.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philip Spinhoven, Prof. dr.
Organizational Affiliation
Leiden University, Institute for Psychological Research
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Arnold A.P. van Emmerik, Dr.
Organizational Affiliation
Leiden University, Clinical Psychology Unit
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Anne E. van Giezen, Dr.
Organizational Affiliation
Leiden University, Institute for Psychological Research, Clinical Psychology Unit
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Anne E.M. Speckens, Prof. dr.
Organizational Affiliation
Radboud University Medical Center
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Suzanne de Klerk, MSc.
Organizational Affiliation
Leiden University, Institute for Psychological Research, Clinical Psychology Unit
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Medical Centre St. Radboud
City
Nijmegen
State/Province
Gelderland
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Speckens, Prof. dr.
Email
a.speckens@psy.umcn.nl
First Name & Middle Initial & Last Name & Degree
de Klerk, MSc
Email
S.deklerk@psy.umcn.nl
Facility Name
Leiden University Medical Centre
City
Leiden
State/Province
Zuid-Holland
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne van Giezen, PhD
Phone
+31-71-527-3729
Email
Giezen@fsw.leidenuniv.nl
Facility Name
Rivierduinen Mental Health Centre
City
Leiden
State/Province
Zuid-Holland
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne van Giezen, PhD
Phone
+715273729
Email
Giezen@fsw.leidenuniv.nl

12. IPD Sharing Statement

Learn more about this trial

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

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