Family Based Treatment of Depressed Adolescents

NCT ID: NCT00700609

Last Updated: 2015-07-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

PHASE2

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-06-30

Study Completion Date

2009-12-31

Brief Summary

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The purpose of this project is to assess the effectiveness of a family-based therapy (Attachment based family therapy-ABFT) for Norwegian adolescents (13-17 years) referred to specialist mental heath clinics.

Detailed Description

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Depression is a major public health concern among adolescents. Research suggests that it not only is prevalent among adolescents (as many as 20% of adolescents have a depressive episode by the age of 18), but its effects last well into adulthood. Although available studies of psychosocial and pharmacological interventions show promise, there are concerns regarding their effectiveness and possible side effects like increase in suicidal ideation. Family conflict is not only an effect of depression, but also a risk factor for depression. High conflict and dysfunction, have consistently been shown to increase risk for depression. As such, family treatments that target risk and protective factors (e.g., quality of parent-child interaction, parental monitoring) for depression seem promising to reduce depression. The current study is a randomized clinical trail aimed at assessing the effectiveness of a 12-week family based intervention for depressed adolescents (Attachment based family therapy- ABFT). Adolescents referred to specialist mental health hospital in south-west Norway (Stavanger University Hospital) will be randomized to either ABFT or treatment as usual (TAU). Therapists administering both the experimental and control group intervention are regular staff clinicians. Outcome assessments would be carried out at baseline, 6, 12 and 26 weeks by raters blind to the condition of the treatment.

Conditions

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Depressive Disorder Mood Disorder Major Depression

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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1

Attachment Based Family Therapy (ABFT)

ABFT developed by Dr. Guy Diamond and colleagues is a brief, 12 week, manualized family-based intervention.

Group Type EXPERIMENTAL

Attachment Based Family therapy (ABFT)

Intervention Type BEHAVIORAL

Attachment-Based Family Therapy (ABFT) is a brief manualized therapy designed exclusively for depressed adolescents and aims at reducing adolescent depression by improving family communication and trust.

2

Treatment as usual (TAU)

No attempt is made to standardize TAU. Regular clinical staff will provide mental health services.

Group Type ACTIVE_COMPARATOR

Attachment Based Family therapy (ABFT)

Intervention Type BEHAVIORAL

Attachment-Based Family Therapy (ABFT) is a brief manualized therapy designed exclusively for depressed adolescents and aims at reducing adolescent depression by improving family communication and trust.

Interventions

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Attachment Based Family therapy (ABFT)

Attachment-Based Family Therapy (ABFT) is a brief manualized therapy designed exclusively for depressed adolescents and aims at reducing adolescent depression by improving family communication and trust.

Intervention Type BEHAVIORAL

Other Intervention Names

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ABFT TAU

Eligibility Criteria

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Inclusion Criteria

* 13-17 years
* Referred to specialist mental health hospital
* HAM-D score of \>14
* Meets diagnostic criteria for major depressive disorder or depression NOS
* Have a parent or guardian willing to participate

Exclusion Criteria

* Suicidal and require in-patient care
* Low intellectual abilities
* Current psychosis
* primary caregiver unwilling to participate
Minimum Eligible Age

13 Years

Maximum Eligible Age

17 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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The Research Council of Norway

OTHER

Sponsor Role collaborator

Helse Stavanger HF

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pravin Israel, Ph.D

Role: PRINCIPAL_INVESTIGATOR

Helse Stavanger HF

Locations

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Department of Child and Adolescent Psychiatry, Stavanger University Hospital

Stavanger, Rogaland, Norway

Site Status

Countries

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Norway

Other Identifiers

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18651

Identifier Type: -

Identifier Source: org_study_id

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