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Development, Feasibility and Acceptability of an iCBT Intervention for Adolescents With Anxiety

Primary Purpose

Anxiety Disorders

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
CoolMinds
Sponsored by
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Anxiety Disorders

Eligibility Criteria

12 Years - 17 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Between 12 and 17 years of age Primary anxiety diagnosis Must have the ability to read and write Danish Must have Internet access Must have a parent able to participate in the treatment alongside the adolescent Exclusion Criteria: Specific phobia of blood-injection-injury type An autism spectrum disorder Psychotic symptoms Bipolar disorder Current suicidal ideation or self-mutilating behavior Current alcohol or substance abuse Moderate to severe depression Current eating disorder

Sites / Locations

  • University of Southern Denmark

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Planned therapist feedback iCBT

On-demand therapist feedback iCBT

Arm Description

Participants in the planned therapist feedback iCBT condition will receive the iCBT intervention with planned feedback after each completed module. The therapist may spend a max. of 15 minutes giving feedback per module.

Participants in the on-demand therapist feedback iCBT condition will receive the intervention with on-demand feedback that is participant-initiated. The therapist may spend a max. of 15 minutes giving feedback per module.

Outcomes

Primary Outcome Measures

The Youth Online Diagnostic Assessment (YODA)
An online diagnostic assessment tool that assesses DSM-5 anxiety disorders and specific phobias. Each present diagnosis is assigned a clinician-rated severity score ranging from 0 (minimal/absent) to 4 (pervasive). Typically subclinical disorders would receive a rating of 0 or 1, and clinical disorders a rating of 1 to 4.
Spence Children's Anxiety Scale (SCAS-C/P)
A 44-item self-report questionnaire assessing anxiety symptoms of six different anxiety disorders in DSM-IV: generalized anxiety, panic/agoraphobia, social phobia, separation anxiety, obsessive compulsive disorder and physical injury fears. Symptoms are rated on a 4-point frequency scale ranging from 0 (never) to 3 (always) (min. = 0; max. = 114). A higher score indicates increased symptom severity. The Danish version has demonstrated good psychometric properties

Secondary Outcome Measures

Child Anxiety Life Interference Scale (CALIS)
CALIS measures the impact of youth anxiety on various areas of life functioning such as school, extracurricular activities, family life and friendships. Impact is reported on a 5-point severity scale ranging from 0 (not at all) to 4 (a lot) (min. = 0; max = 56). A summed score of all items is used to indicate level of impact, where a higher score indicates greater impairment. CALIS has shown satisfactory internal consistency and moderate test-retest reliability.
The Patient Health Questionnaire (PHQ-9)
A 9-item questionnaire used to measure youth depressive symptoms and suicidal ideation within the past 2 weeks. Symptoms are rated on a frequency scale ranging from 0 (not at all) to 3 (nearly everyday). The symptoms are evaluated independently by adolescents. A summed score of all 9 items is used to indicate symptom severity (min. = 0; max. = 27), where a higher score indicates greater severity and possible presence of a depressive disorder.

Full Information

First Posted
September 25, 2023
Last Updated
October 4, 2023
Sponsor
University of Aarhus
Collaborators
University of Southern Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT06076954
Brief Title
Development, Feasibility and Acceptability of an iCBT Intervention for Adolescents With Anxiety
Official Title
Development, Feasibility and Acceptability of an Internet-based Cognitive Behavioral (iCBT) Intervention for Adolescents With Anxiety Disorders
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
December 15, 2022 (Actual)
Primary Completion Date
June 30, 2023 (Actual)
Study Completion Date
July 30, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
Collaborators
University of Southern Denmark

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of the feasibility study is twofold: 1) to test the feasibility of the study design, and 2) to test the preliminary efficacy and the acceptability of a new iCBT intervention when delivered with different levels of therapist support. The feasibility trial will provide important information on the initial participant responses, and on how to properly collect data in the subsequent RCT. The feasibility trial is conducted as a randomized study with 16 participants consisting of two conditions: 1) guided iCBT, and 2) on-demand iCBT, both to be completed over a 14-week period. Participants in the guided iCBT condition will receive the new iCBT intervention with planned feedback after each completed module. Participants in the on-demand iCBT condition will receive the intervention with on-demand feedback that is participant-initiated. In both conditions, the therapist may spend a max. of 15 minutes giving feedback per module. As there is no evidence on what amount of therapist support is sufficient for adolescents, the allowed time spent giving feedback will not differ between the two conditions in the feasibility trial. Thus, data on engagement will be collected to inform how the two treatment conditions differ. The trial includes data points at pre-treatment (T1) and post-treatment (T2) where the same measures will be administered as are planned in the RCT. Acceptability of the intervention will be investigated by conducting semi-structured interviews with the participants. The interview will include an evaluation of the intervention, client satisfaction and potential reasons for drop out. The results from the feasibility trial will be used to inform the subsequent RCT and to revise the intervention, procedures, and conditions if needed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety Disorders

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Planned therapist feedback iCBT
Arm Type
Experimental
Arm Description
Participants in the planned therapist feedback iCBT condition will receive the iCBT intervention with planned feedback after each completed module. The therapist may spend a max. of 15 minutes giving feedback per module.
Arm Title
On-demand therapist feedback iCBT
Arm Type
Experimental
Arm Description
Participants in the on-demand therapist feedback iCBT condition will receive the intervention with on-demand feedback that is participant-initiated. The therapist may spend a max. of 15 minutes giving feedback per module.
Intervention Type
Behavioral
Intervention Name(s)
CoolMinds
Other Intervention Name(s)
Internet-based cognitive behavioral therapy, Technology-delivered cognitive behavioral therapy, iCBT
Intervention Description
CoolMinds consists of 11 adolescent sessions and 9 parent sessions to be completed simultaneously during a 14-week treatment period. The main components comprise psychoeducation, cognitive restructuring, exposure therapy, and relapse prevention. The parent program also comprises information on how to handle school absenteeism for parents and teachers or pedagogues. The intervention is mainly transdiagnostic within the anxiety disorders but also includes diagnosis specific modules and content allowing for more personalized treatment. The treatment is delivered via a telephone app but can also be accessed via computer.
Primary Outcome Measure Information:
Title
The Youth Online Diagnostic Assessment (YODA)
Description
An online diagnostic assessment tool that assesses DSM-5 anxiety disorders and specific phobias. Each present diagnosis is assigned a clinician-rated severity score ranging from 0 (minimal/absent) to 4 (pervasive). Typically subclinical disorders would receive a rating of 0 or 1, and clinical disorders a rating of 1 to 4.
Time Frame
Pre-intervention, post-intervention (12 weeks after commencing treatment)
Title
Spence Children's Anxiety Scale (SCAS-C/P)
Description
A 44-item self-report questionnaire assessing anxiety symptoms of six different anxiety disorders in DSM-IV: generalized anxiety, panic/agoraphobia, social phobia, separation anxiety, obsessive compulsive disorder and physical injury fears. Symptoms are rated on a 4-point frequency scale ranging from 0 (never) to 3 (always) (min. = 0; max. = 114). A higher score indicates increased symptom severity. The Danish version has demonstrated good psychometric properties
Time Frame
Pre-intervention, post-intervention (12 weeks after commencing treatment)
Secondary Outcome Measure Information:
Title
Child Anxiety Life Interference Scale (CALIS)
Description
CALIS measures the impact of youth anxiety on various areas of life functioning such as school, extracurricular activities, family life and friendships. Impact is reported on a 5-point severity scale ranging from 0 (not at all) to 4 (a lot) (min. = 0; max = 56). A summed score of all items is used to indicate level of impact, where a higher score indicates greater impairment. CALIS has shown satisfactory internal consistency and moderate test-retest reliability.
Time Frame
Pre-intervention, post-intervention (12 weeks after commencing treatment)
Title
The Patient Health Questionnaire (PHQ-9)
Description
A 9-item questionnaire used to measure youth depressive symptoms and suicidal ideation within the past 2 weeks. Symptoms are rated on a frequency scale ranging from 0 (not at all) to 3 (nearly everyday). The symptoms are evaluated independently by adolescents. A summed score of all 9 items is used to indicate symptom severity (min. = 0; max. = 27), where a higher score indicates greater severity and possible presence of a depressive disorder.
Time Frame
Pre-intervention, post-intervention (12 weeks after commencing treatment)
Other Pre-specified Outcome Measures:
Title
Client Satisfaction Questionnaire-8 (CSQ-8)
Description
An 8-item questionnaire used to measure general satisfaction with a received treatment. Satisfaction is reported using a 4-point scale ranging from 1 (lowest degree of satisfaction) to 4 (highest degree of satisfaction). A summed score of all items is used to indicate level of satisfaction (min = 8; max. = 32). The scale has shown high internal consistency and concurrent validity.
Time Frame
Post-intervention (12 weeks after commencing treatment)
Title
EuroQol-5 Dimension Youth (EQ-5D-5L)
Description
A 5-item self-report questionnaire assessing quality of life and self-rated health. The items cover five domains: mobility, selfcare, usual activities, pain/discomfort, and anxiety and depression. Each domain is assigned a score from 1 (no health problems) to 3 (a lot of health problems) and based on these scores, a unique health state can be identified for each participant.
Time Frame
Pre-intervention, post-intervention (12 weeks after commencing treatment)
Title
Negative Effects Questionnaire (NEQ)
Description
A 20-item questionnaire used to monitor the occurrence of negative effects in psychological treatments. Participants are asked to report whether specific things have occurred or not during treatment, how negatively it affected them, and whether the negative affect is attributed to the received treatment or other circumstances. The items can be summed together in order to get a frequency measure of the number of negative effects the respondents have experienced, divided by treatment or other circumstances. NEQ shows acceptable psychometric properties.
Time Frame
Post-intervention (12 weeks after commencing treatment)
Title
Systems Usability Scale (SUS)
Description
A 10-item questionnaire used to assess the subjective experience of usability of a computer system. Participants are asked to score 10 different statements about the computer system on a 5-point scale from 0 (strongly disagree) to 4 (strongly agree). A higher summed score indicates greater comfortability with the computer system. A Danish version of the SUS has been validated in a mental health care setting.
Time Frame
Post-intervention (12 weeks after commencing treatment)
Title
Engagement with the program: Wordcount
Description
Number of words in the in-program text modules and number of words in messages sent by both participant and therapist.
Time Frame
Post-intervention (12 weeks after commencing treatment)
Title
Engagement with the program: number of logins
Description
Number of logins in the digital platform.
Time Frame
Post-intervention (12 weeks after commencing treatment)
Title
Engagement with the program: Time spent on feedback
Description
Therapist time spent giving feedback reported in minutes.
Time Frame
Post-intervention (12 weeks after commencing treatment)
Title
Demography
Description
Sociodemographic measures include participants' age and gender, and parents' level of education, and primary caregiver in case of single parents.
Time Frame
Pre-intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Between 12 and 17 years of age Primary anxiety diagnosis Must have the ability to read and write Danish Must have Internet access Must have a parent able to participate in the treatment alongside the adolescent Exclusion Criteria: Specific phobia of blood-injection-injury type An autism spectrum disorder Psychotic symptoms Bipolar disorder Current suicidal ideation or self-mutilating behavior Current alcohol or substance abuse Moderate to severe depression Current eating disorder
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kim Mathiasen, PhD
Organizational Affiliation
University of Southern Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Southern Denmark
City
Odense
State/Province
Region Of Southern Denmark
ZIP/Postal Code
5000
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No

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Development, Feasibility and Acceptability of an iCBT Intervention for Adolescents With Anxiety

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