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Mentalization-Based Group Therapy for Adolescents

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ClinicalTrials.gov Identifier: NCT02771691
Recruitment Status : Completed
First Posted : May 13, 2016
Last Update Posted : June 4, 2019
Sponsor:
Collaborator:
NHS Lothian
Information provided by (Responsible Party):
University of Edinburgh

Brief Summary:
This is a prospective parallel group design of group-based Mentalization-Based Therapy for Adolescents (MBT-A) through a pilot randomised controlled trial comparing group-based MBT-A plus treatment as usual (TAU) to TAU alone. As a pilot study, we aim to determine: the effectiveness of our recruitment strategies; compliance with protocol/procedures; trends towards reduced self-harm.

Condition or disease Intervention/treatment Phase
Deliberate Self-Harm Other: Mentalization-Based Group Therapy for Adolescents Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 53 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Efficacy of Mentalization-Based Group Therapy for Adolescents: A Pilot Randomised Controlled Trial
Study Start Date : February 2016
Actual Primary Completion Date : November 2017
Actual Study Completion Date : November 2017

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Self-Harm

Arm Intervention/treatment
Experimental: MBT therapy plus treatment as usual
Mentalization based group treatment for adolescents plus standard care
Other: Mentalization-Based Group Therapy for Adolescents
No Intervention: Treatment as usual alone
Standard care provided by local Child and Adolescent Mental Health Services



Primary Outcome Measures :
  1. Self-harm as measured by the self-harm sub scale of the Risk-taking and Self-harm Inventory for Adolescents (Vrouva et al, 2010) [ Time Frame: 12 weeks ]
  2. Self-harm and related hospital use as reported in National Health Service patient records [ Time Frame: 12 weeks ]


Information from the National Library of Medicine

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Ages Eligible for Study:   12 Years to 18 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Self-harm behaviour in the past 6 months
  • In receipt of treatment from local Child and Adolescent Mental Health Services
  • Competent and willing to provide written, informed consent.

Exclusion Criteria:

  • Severe learning disability or pervasive developmental disorder
  • Acute psychotic episode
  • Eating disorder in the absence of self-harm.
  • Non-English speaking
  • Current involvement in other ongoing treatment research

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02771691


Locations
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United Kingdom
CAMHS
Edinburgh, Lothian, United Kingdom
Sponsors and Collaborators
University of Edinburgh
NHS Lothian
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: University of Edinburgh
ClinicalTrials.gov Identifier: NCT02771691    
Other Study ID Numbers: ELHF10-595
First Posted: May 13, 2016    Key Record Dates
Last Update Posted: June 4, 2019
Last Verified: November 2017
Keywords provided by University of Edinburgh:
Adolescent
Additional relevant MeSH terms:
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Self Mutilation
Self-Injurious Behavior
Behavioral Symptoms
Wounds and Injuries