Skip to content

School Based Low-intensity Cognitive Behavioral Intervention for Anxious Youth

School Based Low-intensity Cognitive Behavioral Intervention for Anxious Youth. A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02279251
Acronym
LIST
Enrollment
313
Registered
2014-10-31
Start date
2013-10-31
Completion date
2020-11-01
Last updated
2021-08-18

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

Conditions

Anxiety

Keywords

Anxiety, adolescents, school-based, low-intensity CBT

Brief summary

The study will evaluate two group CBT interventions delivered by school health nurses, in cooperation with community psychologist and mental health care personnel, to adolescents with mild to moderate levels of anxiety symptoms. The two interventions have different intensity (5 versus 10 group meetings). The two group interventions will be compared to a waitlist control group.

Detailed description

Anxiety disorders are among the major mental health problems in children and adolescents, with regard to prevalence and long-term consequences. Cognitive behavioural therapy (CBT) has proven to be effective as treatment, early intervention and prevention of youth anxiety disorders. The majority of youth with anxiety problems, however, is not in contact with mental health services and do not receive effective help. This is due to shortage of personnel, resources and time among mental health-personal delivering treatment, as well as health services not being easily accessable for adolescents. School-based, low-intensity early intervention programs (indicated prevention) may improve access to effective treatment for youth with internalizing problems, and also promote more effective use of health services. The present study is a multi-site randomized controlled study with early intervention to be conducted within the primary health care service in three parts of Norway; including nine municipalities from west, east and south of Norway. A brief CBT program will be compared to a longer CBT program, and a wait-list control group. The effects will be evaluated with regard to decrease in youth internalizing symptoms. The CBT interventions are given to adolescents with mild to moderate levels of anxiety symptoms. Interventions are delivered by trained school-health nurses in collaboration with and/or supervised by experienced CBT therapists. The study involves researchers from three research environments in Norway, and collaboration with prominent international researchers from USA and Australia.The study has potential impact on how to deliver effective low-threshold interventions to anxious youth.

Interventions

BEHAVIORALVÅG

Low-intensity CBT intervention

BEHAVIORALCHILLED

Standard length CBT intervention

Sponsors

The Research Council of Norway
CollaboratorOTHER
Modum Bad
CollaboratorOTHER
Sorlandet Hospital HF
CollaboratorOTHER_GOV
NORCE Norwegian Research Centre AS
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to 16 Years
Healthy volunteers
No

Inclusion criteria

1. An overall score of \> 25 on the anxiety inventory Spence Children's Anxiety Scale (SCAS) and a score of \> 1 on the first question of the Children's Anxiety Life Interference Scale (CALIS), indicating that anxiety interferes with daily life of the youth, rated either by the adolescents or by one parent. 2. The adolescent and at least one parent understand and read Norwegian. 3. Assent from the youth and signed informed consent from the parent.

Exclusion criteria

The adolescent has a behavior that makes participation in groups with other adolescents challenging. This is evaluated by the school nurse, based on information from the adolescent, the parent and the teacher. In each case, the school nurse makes an evaluation based on the following questions: 1. Is the adolescent able to follow group-rules? 2. Will the adolescent behave in ways that disrupts the group? 3. Does the adolescent have learning problems to an extent that will make it difficult to follow the group program?

Design outcomes

Primary

MeasureTime frameDescription
Spence Children's Anxiety ScaleChanges from baseline to 4 weeks, 10 weeks, and 1 yearSelf-reported (child and parent version) child anxiety symptoms, 38 items questionnaire, rated at a 4-point scale.
Children Anxiety Life Interference ScaleChanges from baseline to 4 weeks,10 weeks, and 1 yearSelf-reported (child and parent version) of degree of life interference of child anxiety symptoms

Secondary

MeasureTime frameDescription
Short Mood and Feeling QuestionnaireChanges from baseline to 4 weeks,10 weeks,and 1 yearQuestionnaire measuring symptoms of depression (child and parent version)
Questionnaire for Measuring Health-Related Quality of Life Children and Adolescents (KINDL-R)Changes from baseline to 10 weeks, and 1 yearQuestionnaire (child and parents version) measuring quality of life in youth
Clinical Global Impression Scale, severity/improvement (CGI-S/I)Changes from baseline to 10 weeks, and 1 yearThe clinician's (i.e. the school health nurse) global assessment of level of youth anxiety
Sleep problemsChanges from baseline, up to 10 weeks, and after 1 yearQuestionnaire (youth) on variables related to sleep (sleep duration, insomnia etc.)

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026