MedPath

Internet-delivered Cognitive Behavioural Therapy for Adolescents With Anxiety

Not Applicable
Completed
Conditions
Anxiety
Interventions
Behavioral: Guided-ICBT with chat
Behavioral: Guided-ICBT for adolescents with anxiety
Behavioral: Guided-ICBT with learning support and chat
Behavioral: Guided-ICBT with learning support
Registration Number
NCT03441490
Lead Sponsor
Linkoeping University
Brief Summary

The purpose of this study is to evaluate the effects of learning support and chat on treatment outcome in internet-administrated cognitive behaviour therapy (ICBT) for adolescents with anxiety.

Detailed Description

The study is set up as a factorial design with two independent variables: 1: Learning support and 2: chat-sessions in real time. The intervention tested is based on cognitive behavior therapy delivered over the internet via a secure treatment platform. Participants in the study are recruited from the general public via social media. The intervention is in Swedish.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
120
Inclusion Criteria
  • Be between the ages of 15-19 years old
  • Have symptoms of anxiety, anxiety disorder
Exclusion Criteria
  • Suicidal ideation
  • Alcohol addiction
  • other major primary psychiatric disorder
  • Ongoing psychological treatment
  • recent (during last 4 weeks) change in psychiatric medication

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
ICBT chatGuided-ICBT with chatInternet-based cognitive behavioural therapy with therapeutic guidance through chat
ICBT standardGuided-ICBT for adolescents with anxietyInternet-based cognitive behavioural therapy with therapeutic guidance through mail
ICBT with learning support and chatGuided-ICBT with learning support and chatInternet-based cognitive behavioural therapy with learning support and therapeutic guidance through chat
ICBT learning supportGuided-ICBT with learning supportInternet-based cognitive behavioural therapy with learning support and therapeutic guidance through mail
Primary Outcome Measures
NameTimeMethod
Beck Depression Inventory - II (BDI-II)Two weeks pre treatment, two weeks post treatment, six months post treatment and 12 months post treatment

Measures clinical depression. Change from baseline in symptoms two weeks post treatment and at 12 months post treatment.

Beck Anxiety Inventory (BAI)Two weeks pre treatment, two weeks post treatment, six months post treatment and 12 months post treatment

Measures clinical anxiety. Change from baseline in symptoms two weeks post treatment and at 12 months post treatment.

Secondary Outcome Measures
NameTimeMethod
Generalised Anxiety Disorder (GAD-7)First week of treatment and then once a week during the treatment-period, two weeks post treatment, six months post treatment and 12 months post treatment.

Measures severity of generalised anxiety.

Agoraphobic Cognitions Questionnaire (ACQ)Two weeks pre treatment, two weeks post treatment, six months post treatment and 12 months post treatment

Measures fearful cognitions associated with panic attacks and agoraphobia. The ACQ consists of 14 items which will be scored as a total scale in this study. worry. Respondents rates each item on a 5-point Likert scale consisting of never (1), Thought never occurs (2), Thought rarely occurs (3) Thought occurs during half of the times when I am nervous (4) Thought usually occurs (5) Thought always occurs when I am nervous. ACQ can be divided into two subscales: Loss of Control and Physical Concerns. Each of the subscales consists of 7 items.The total scores (or the subscales) are calculated by averaging the responses to the individual items composing that score. Higher scores indicates higher levels of fearful cognitions. Change from baseline in symptoms two weeks post treatment and at 12 months post treatment.

Penn State Worry Questionnaire for Children (PSWQ - C)Two weeks pre treatment, two weeks post treatment, six months post treatment and 12 months post treatment

Measures the tendency of youth to engage in excessive, generalized and uncontrollable worry. Respondents rates each item on a 4-point Likert scale consisting of never (0), sometimes (1), often (2) and always (3). The scores from each item are summed together to yield a total score that ranges from 0-42, with higher scores reflecting higher levels of worry. Change from baseline in symptoms two weeks post treatment and at 12 months post treatment.

Mini-Social Phobia Inventory (MINI-SPIN)Two weeks pre treatment, two weeks post treatment, six months post treatment and 12 months post treatment

Measures clinical social phobia. Change from baseline in symptoms two weeks post treatment and at 12 months post treatment.

Satisfaction With Life Scale (SWLS)Two weeks pre treatment, two weeks post treatment, six months post treatment and 12 months post treatment

Measures global cognitive judgements of one's life satisfacation as a whole, on a 5-item scale. Respondants rates how much they agree or disagree on a 7-pont scale ranging from (7) strongly agree to (1) strongly disagree, where higher scores indicates higher levels of life satisfaction. Change from baseline in symptoms two weeks post treatment and at 12 months post treatment.

Alcohol Use Disorders Identification Test (AUDIT)Two weeks pre treatment, two weeks post treatment, six months post treatment and 12 months post treatment

Measures alcohol consumption, drinking behaviors, and alcohol-related problems. Change from baseline in symptoms two weeks post treatment and at 12 months post treatment.

Rosenberg Self-Esteem Scale (RSES)Two weeks pre treatment, two weeks post treatment, six months post treatment and 12 months post treatment

Evaluates individual self-esteem. The scale is a ten item Likert scale with items answered on a four point scale, from (0) strongly agree to strongly disagree (3), where higher scores indicates higher self-esteem. Change from baseline in symptoms two weeks post treatment and at 12 months post treatment.

Knowledge of CBT strategies (developed by the research group)Two weeks pre treatment, two weeks post treatment, six months post treatment and 12 months post treatment

A brief 16-item questionnaire that measures explicit, declarative knowledge about core CBT-principles and therapeutic points. Higher scores indicates more knowledge. Change from baseline in symptoms two weeks post treatment and at 12 months post treatment.

Trial Locations

Locations (1)

Linköping University

🇸🇪

Linköping, Sweden

© Copyright 2025. All Rights Reserved by MedPath