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CBT for Adolescents With Excessive Worry

Cognitive Behavioral Therapy for Adolescents With Excessive Worry - a Case Series

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02978963
Acronym
BiPOro
Enrollment
12
Registered
2016-12-01
Start date
2016-10-31
Completion date
2017-10-31
Last updated
2017-12-22

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

Conditions

Excessive Worry

Keywords

Excessive worry, Worry, Adolescents, Intolerance of uncertainty

Brief summary

This case series aims to test the feasibility and acceptability of streamlined cognitive behavioral therapy (CBT) for adolescents with excessive worry. The treatment protocol focuses on reducing intolerance of uncertainty and the hypothesis is that this will help reduce worry.

Detailed description

This pilot study aims to test a new form of Cognitive Behavioral Therapy for adolescents with excessive worry. The investigators will include 12 participants with excessive worry and test the treatment which focuses on reducing intolerance of uncertainty (IU) in order to reduce worry. Participants will be randomized to either one, two or three weeks of weekly baseline measurements prior to starting treatment, and will thus work as their on controls in this case series design. Primary outcome measures will be collected at 12 weeks after treatment start. Participants will be followed up at three months after treatment.

Interventions

BEHAVIORALCognitive behavioral therapy

CBT focused on reducing intolerance of uncertainty

Sponsors

Region Stockholm
CollaboratorOTHER_GOV
Karolinska Institutet
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
13 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* A score on PSWQ-C of at least 22 * Age between 13 and 17 years * Ability to read and write in Swedish * A parent or caregiver that is able to co-participate in the treatment * Participants on psychotropic medication must have been on a stable dose for the last 6 weeks prior to baseline assessment

Exclusion criteria

* Diagnosis of autism spectrum disorder, psychosis, bipolar disorder or severe eating disorder * Present risk of suicide * Ongoing substance dependence * Occurrence of domestic violence * Completed CBT for any anxiety disorder within the last 6 months (defined as at least 5 sessions of CBT including in vivo exposure sessions)

Design outcomes

Primary

MeasureTime frameDescription
Penn State Worry Questionnaire for Children (PSWQ-C)At 12 weeks after treatment startsChild and parent version

Secondary

MeasureTime frameDescription
Brief Intolerance of Uncertainty Scale (Brief IUS)Baseline, weekly during treatment, 12 weeks after treatment starts, and three months after treatment has endedSelf rated tolerance to treatment
Mini International Neuropsychiatric Interview for Children and Adolescents (MINI-KID)Baseline, 12 weeks after start of treatment and three month after treatment has ended.Diagnostic interview
Clinical Global Impression - Severity (CGI-S)Baseline, 12 weeks after start of treatment and three month after treatment has ended.Clinician rated severity of symptoms
Clinical Global Impression - Improvement (CGI-I)At 12 weeks after start of treatment and three month after treatment has ended.Clinician rated improvement after treatment
Children's Global Assessment Scale (CGAS)Baseline, 12 weeks after start of treatment and three month after treatment has ended.Clinician rated global functioning
Brief Why Worry-II (Brief WW2)Baseline, weekly during treatment, 12 weeks after treatment starts, and three months after treatment has endedSelf rated positive assumptions of worry
Negative Problem Orientation Questionnaire (NPOQ)Baseline, weekly during treatment, 12 weeks after treatment starts, and three months after treatment has endedSelf rated negative problem orientation
Revised Children´s Anxiety and Depression Scale (RCADS-C)Baseline, 12 weeks after start of treatment and three month after treatment has ended.Child and parent version.
Education, Work and Social Adjustment Scale (EWSAS)Baseline, 12 weeks after start of treatment and three month after treatment has ended.Child and parent version.
Brief Cognitive Avoidance Questionnaire (Brief CAQ)Baseline, weekly during treatment, 12 weeks after treatment starts, and three months after treatment has endedSelf rated cognitive avoidance

Countries

Sweden

Outcome results

None listed

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