Major Depressive DisorderIDANCT04977856
Efficacy and Cost-effectiveness of Internet-delivered CBT for Adolescents With Depression
A study testing Behavioral activation (BA) and Regular care within primary or secondary mental health care for children in people with Major Depressive Disorder, run by Region Stockholm at 1 site in Sweden.
Trial summary
Adolescent depression is a prevalent and impairing condition that can be effectively treated with Cognitive Behavior Therapy (CBT). However, a majority of adolescents do not have access to CBT. Internet-delivered CBT (ICBT) has been suggested as a way to increase availability to effective psychological treatments. Read more about this study
- Who is it for?
- Ages 13 to 17 years
- Conditions the study is for
- Major Depressive Disorder
- What is being tested?
- Behavioral activation (BA) and Regular care within primary or secondary mental health care for children
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 219 participants
- Where
- 1 siteSweden
- Study dates
- 10 Sep 2021to 12 Jun 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 13 to 17 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- 13-17 years of age,
- A diagnosis of mild to moderate MDD based on the DSM-5,
- Willing to be randomized to either of the three treatment arms,
- Basic proficiency in Swedish, both adolescent, and a participating caregiver
- Regular access to a desktop, laptop computer connected to the internet, as well as a mobile phone,
- If using medication with antidepressants, central stimulants, or neuroleptics it has to be unchanged at least 6 weeks prior to inclusion, and
- A minimum of one caregiver that is able to co-participate in the treatment.
Who cannot join
- The presence of psychiatric problems requiring immediate treatment (e.g., high risk of suicide, psychosis, severe self-injury, bipolar disorder, clinical eating disorder, alcohol/substance abuse),
- Social problems requiring immediate action (e.g., ongoing abuse in the family, high and prolonged absence from school);
- Previous psychological treatment for MDD (CBT, interpersonal psychotherapy (IPT), or BA) for a minimum of at least 3 sessions within the last 12 months prior to assessment.
- Current use of benzodiazepines.
- Ongoing psychological treatment for any psychiatric disorder.
Trial locations and contacts
1 site in 1 country.
Sweden1 site
BUP Internetbehandling, BUP Forsknings- och utvecklingscentrum i Stockholm
Stockholm, Stockholm County, 11364
About this study
Official title: Efficacy and Cost-effectiveness of Internet-delivered Cognitive Behavior Therapy for Adolescents With Mild to Moderate Depression: A Randomized Controlled Trial of Guided and Self-guided ICBT vs. Treatment as Usual
Adolescent depression is a prevalent and impairing condition that can be effectively treated with Cognitive Behavior Therapy (CBT). However, a majority of adolescents do not have access to CBT. Internet-delivered CBT (ICBT) has been suggested as a way to increase availability to effective psychological treatments. Yet, the research on ICBT for adolescents has been lagging behind significantly.
The overall aim of this research project is to increase the availability of evidence-based psychological treatments for adolescents with depression by developing and evaluating internet-delivered Cognitive Behavior Therapy (ICBT) for this target group. The main objectives are to establish the efficacy, cost-effectiveness, and long-term effects of the guided and self-guided ICBT for adolescents with mild to moderate depression in a randomized controlled trial (RCT) with three-arms; guided ICBT (with therapist-support) and self-guided ICBT (without therapist-support) vs treatment as usual (TAU).
Read the detailed description
Primary and secondary objectives
Primary objective:
- To determine the clinical efficacy of Guided and Self-guided ICBT for depression for reducing depressive symptom severity (as measured by the CDRS-R (27) in adolescents with mild and moderate major depressive disorder (MDD), compared with an active control intervention (treatment as usual within primary or secondary child and adolescent mental health care). The primary endpoint is the follow-up 3 months post-treatment.
Secondary objectives:
- To establish the 12-month durability of the treatment effects.
- To conduct a health-economic evaluation of guided ICBT for depression and self-guided ICBT for depression, compared with TAU, from multiple perspectives, both in the short term (primary endpoint) and the long term (12-month follow-up).
- To investigate potential mediators behind a potential treatment effect of ICBT.
Research questions:
- Is guided and self-guided ICBT more efficacious than TAU in regard to the reduction of depressive symptoms?
- Is guided and self-guided ICBT more cost-effective than TAU?
- Is self-guided ICBT more cost-effective than guided ICBT?
- Are the therapeutic gains of ICBT maintained long term (i.e., 1 year after the intervention)?
- Do changes in activation and avoidance (BADS) mediate changes at post-treatment in self-reported depressive symptoms (QIDS-A-17) in adolescents receiving ICBT (with or without therapist support), but not in the control group (treatment as usual)?
- Conditions
- Major Depressive Disorder
- Being tested
- Behavioral activation (BA), Regular care within primary or secondary mental health care for children
- Medical subject headings
- Depressive Disorder, Major
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Behavioral activation (BA)Behavioural
The main goal of the BA is to increase engagement in values-based activities and decrease avoidant behaviors that serve to maintain depression. The adolescent will learn about depression, how behavioral activations works, monitor their own activities, plan and do more values-based activities and deal with obstacles to getting in touch with positive reinforcement, such as avoidance behaviors.
Regular care within primary or secondary mental health care for childrenOther
Regular care (supportive therapy, waitlist, psychological treatments, drugs, or a combination of different interventions)
| Study group | Role | What they receive |
|---|---|---|
| Guided ICBT | Experimental | Participants in guided ICBT will receive internet-delivered CBT with therapist support. The treatment consists of 8 online modules with interactive features such as videos and illustrations, delivered over a maximum of 10 weeks. The main treatment focus is behavioral activation. The adolescent and the caregiver are provided with their own separate programs and login to the treatment platform. The caregiver's program also consists of 8 chapters, including psychoeducation about depression and how to support their adolescent in treatment. The adolescents and caregivers have regular contact with a personal assigned therapist via written text messages in the platform. Participants are typically in contact with their therapist several times a week. The adolescent and caregiver can continue to access all treatment modules for the whole follow-up period (3 months), but without therapist-support. Receives: Behavioral: Behavioral activation (BA) |
| Self-guided ICBT | Experimental | The self-guided arm is identical to the guided arm, however without the therapist support. To ensure patient safety, there will be clear instructions to the patients and primary caregivers on how to get in contact with the study team in case of acute problems, and there will be clinical routines to detect and manage deterioration or suicidal tendencies. Receives: Behavioral: Behavioral activation (BA) |
| Treatment as usual (TAU) | Active comparator | Participants randomized to TAU, will be referred to the local CAMH's or primary care unit for children and youths and will be free to receive any treatment, either psychosocial, medical, or a combination of both. The content of TAU and the treatment techniques used will be monitored. Receives: Other: Regular care within primary or secondary mental health care for children |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change from baseline in clinician-rated depressive scores on Children's Depression Rating Scale - Revised (CDRS-R)
CDRS-R is a semi-structured clinician interview, assessing level of depressive symptomatology. Total range is 17-113, with higher values representing a worse outcome.
Measured: week 0, week 10, at 3 and 12 months follow-up
Secondary outcomes (19)
Clinical Global Impression Scale - Severity (CGI-S)
CGI-S was developed to assess how mentally ill a specific patient compared to a particular patient population (e.g. with major depressive disorder) at a certain time. It consists of a single item rated on a seven-point scale ranging from 1="no symptoms" to 7="extreme symptoms".
Measured: week 0, week 10, at 3 and 12 months follow-up
Clinical Global Impression - Improvement (CGI-I)
CGI-I is developed to assess improvement of psychiatric symptoms for a specific patient compared to baseline. It consists of a single item rated on a seven-point scale ranging from 1="very much improved" to 7="very much worse".
Measured: week 10, at 3- and 12 months follow-up
Children's global assessment scale (CGAS)
The CGAS is a single item 1-100 scale that integrates psychological, social, and academic functioning in children as a measure of psychiatric disturbance. Higher values represent a better outcome.
Measured: week 0, week 10, at 3 and 12 months follow-up
Internet Intervention Patient Adherence Scale (iiPAS)
The iiPAS is a clinician-rated measure of patient adherence to internet-delivered behavioral interventions (38) with 5 items rated on a 0 to 4 Likert scale with total score ranging from 0 to 20, where 0 indicates no adherence and 20 perfect adherence. The scale covers client's work pace, engagement, communication with the therapist, motivation for change, and login frequency. The iiPAS has demonstrated excellent internal consistency and good construct validity as well as a strong association with objective measures of patient activity in ICBT(38). For participants in the self-guided group, we will use an adapted version excluding item 3 since communication with therapist is not applicable, and a research assistant will make the rating at post-treatment.
Measured: Week 10
Anhedonia Scale for Adolescents (ASA)
The ASA is an adolescent specific measure of anhedonia with 14 items with a four graded-scale from 0 (never) to 3 (always), ranging from 0 to 42 points. A higher score indicates more anhedonia. The ASA has high test-retest reliability and good convergent validity with standardized measures of depression.
Measured: week 0, week 10, at 3 and 12 months follow-up
Affective Reactivity Index (ARI)
The ARI is a measure of irritability, consisting of six items with a three graded scale and one item on impairment due to irritability, ranging from 0 to 12 points with higher scores indicating a worse outcome. The ARI has demonstrated an excellent internal consistency and differentiates cases from controls in a clinic a community sample.
Measured: week 0, week 10, at 3 and 12 months follow-up
Behavioral activation of Depression Scale - short form (BADS-S)
The BADS-S is designed to track changes in proposed mediators of behavioral activation, e.g. activation and avoidance. Total range is from 0-54 with higher values indicating higher degree of activation and lower degree of avoidance. Changes during treatment in proposed mediators of behavioral activation on the BADS-S will be reported for the ICBT interventions.
Measured: week 0, weekly during treatment (week 1 to week 10), at 3- and 12 months follow-up
Concomitant interventions
To assess if the adolescent has received other psychological treatments during the trial period, the adolescents answer questions about other potential psychological treatments they have received apart from the interventions included in the trial.
Measured: Week 10 and 3- and 12-months follow-up assessments.
The Client Satisfaction Questionnaire-8 (CSQ-8) - adolescent and parent version
The CSQ-8 is an 8-item self-rated 4-point scale, measuring different aspects of satisfaction with treatment, e.g. perception of quality of treatment, if the treatment adequately addressed their needs and overall satisfaction. Total range is 8 to 32, with higher values indicating higher satisfaction. Mean in total satisfaction scores on the CSQ-8 for each treatment group at end of treatment and at follow-up will be reported.
Measured: week 10
Insomnia Severity Index (ISI)
ISI, a brief screening measure of insomnia, a seven-item scale ranging from 0 to 28 points, with higher values representing a worse outcome.
Measured: week 0, week 10, and at 3- and 12 months follow-up
Kidscreen-10 Index - adolescent and parent version
Kidscreen-10 assess the adolescents' general health-related quality of life. Total range from 10-50, with higher values indicating better health-related quality of life.
Measured: week 0, week 10, at 3- and 12-months follow-up
Need for further treatment - adolescent and parent version
Investigate whether the participant considers her/himself in need of further treatment for her/his depression. The scale ranges from 0 (no need for more treatment) to 4 (great need for more treatment) where higher scores indicate a worse outcome.
Measured: at 3 months follow-up
Negative Effects Questionnaire (NEQ-20) - adolescent and parent version
NEQ-20 investigates participants' negative effects of psychological treatments. Total range is 0-80, with higher values representing a worse outcome.
Measured: Week 10 and 3 months follow-up
The Revised Children's Anxiety and Depression Scale, short (RCADS-S) -adolescent and parent version
The RCADS-S, a shortened version of the Spence Child Anxiety Scale, is a child and parent self-report measure of anxiety- and depression-related psychopathology. Only the anxiety subscales are administered in this study since depressive symptoms are measured thoroughly by other measures. Total range is 0-45, with higher values representing a worse outcome.
Measured: week 0, week 10, 3- and 12 months follow-up
Quick Inventory of Depressive Symptomatology, 17 items (QIDS-17) - adolescent and parent version
The QIDS-17 covers the nine symptoms defined in the Diagnostic Statistical Manual of Mental Disorders (DSM-5) of depression rated in a scale from 0 (none) to 3 (highest) with a sum-range of 0-27. A total score of 6-10 indicates mild depression, 11-15 moderate, 16-20 severe and 21 and above very severe. Response is defined as a reduction by half of the initial score on QIDS-17. Remission is defined as below 6 points on QIDS-17. The QIDS-17 is a very reliable measure and most discriminating at moderate levels of depression.
Measured: week 0, weekly from week 1 to week 10, at 3- and 12 months follow-up
Work and Social Adjustment Scale, youth version (WSAS-Y) - adolescent and parent version
WSAS-Y is a parent- and adolescent-rated scale of impaired functioning in school, everyday life, friends and social life, recreation and hobbies and family and close relationships. The scale generates a global score ranging from 0 to 40, with higher scores indicating greater impairment.
Measured: week 0, week 10, 3- and 12 months follow-up
The Expressed Emotion Adjective Checklist (EEAC)
The EEAC is a validated self-rated questionnaire of the caregiver's positive and negative emotions directed towards the adolescent. The EEAC include 20 adjectives (each scored 1-8 where 1 indicates never and 8 always).
Measured: week 0, week 10, 3- and 12 months follow-up
Trimbos Questionnaire for Costs associated with Psychiatric Illness (TiC-P)
The TiC-P assess healthcare and societal resource use, including for example items on healthcare resource use, medications, school absenteeism, and parental productivity loss. In the present study no health economic evaluations will be conducted. Rather this instrument is included to gain feasibility data in preparation of a planned larger randomized controlled study. Therefore, no data on TiC-P will be reported in this trial.
The TiC-P assess healthcare and societal resource use, including for example items on healthcare resource use, medications, school absenteeism, and parental productivity loss.
Measured: week 0, week 10, at 3- and 12 months follow-up
Treatment credibility - adolescent and parent version
Four qualitative questions about treatment credibility will be administered at week 3, asking how well the treatment suits adolescents with depression, how much they believe this treatment will help him/her, if and to what extent they would recommend this treatment to a friend with depression and how much improvement they expect from the treatment. Each item is scored on a 5-point Likert scale, from 1 to 5. The scale ranges from 4 to 20 points, where a higher score indicates a better outcome.
Measured: week 3
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Jul 2021
- Study start10 Sep 2021
- Primary completion14 Oct 2024
- Study completion12 Jun 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Major Depressive DisorderStudies of the same condition, open and under way.
- More trials run by Region StockholmThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Single-blind parallel-group randomised controlled trial
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 219 participants (actual)
Sponsor and investigators
- Lead sponsor
- Region Stockholm
- Sponsor type
- Other government
- Collaborators
- Karolinska Institutet
- Responsible party
- Sponsor
- Investigators
- Eva Serlachius, PhD, Principal investigator, Karolinska Institutet
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04977856
- Sponsor's protocol ID
- 2021-0859
- Acronym
- IDA
- Status last verified
- Apr 2024
- First submitted
- 13 Jul 2021
- Last updated
- 1 Jun 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Andersson R, Vigerland S, Lenhard F, Ahlen J, Bottai M, Mataix-Cols D, Serlachius E. Single-blinded, randomised, parallel-group, controlled trial comparing the efficacy and cost-effectiveness of therapist- and self-guided internet-delivered behavioural activation versus treatment as usual for adolescents with mild to moderate depression: study protocol. BMJ Open. 2024 Oct 15;14(10):e083507. doi: 10.1136/bmjopen-2023-083507.
PubMed 39414268
Study at a glance
From the registry record, last updated by the sponsor on 1 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Efficacy and Cost-effectiveness of Internet-delivered Cognitive Behavior Therapy for Adolescents With Mild to Moderate Depression: A Randomized Controlled Trial of Guided and Self-guided ICBT vs. Treatment as Usual
- ClinicalTrials.gov ID
- NCT04977856
- Acronym / sponsor ID
- IDA / 2021-0859
- Conditions
- Major Depressive Disorder
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 219 participants (actual)
- Lead sponsor
- Region StockholmOther government
- Collaborators
- Karolinska Institutet
- Study start
- 10 Sep 2021 (actual)
- Primary completion
- 14 Oct 2024 (actual)
- Study completion
- 12 Jun 2025 (actual)
- First posted
- 27 Jul 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Adolescent depression is a prevalent and impairing condition that can be effectively treated with Cognitive Behavior Therapy (CBT). However, a majority of adolescents do not have access to CBT. Internet-delivered CBT (ICBT) has been suggested as a way to increase availability to effective psychological treatments. Yet, the research on ICBT for adolescents has been lagging behind significantly.
The overall aim of this research project is to increase the availability of evidence-based psychological treatments for adolescents with depression by developing and evaluating internet-delivered Cognitive Behavior Therapy (ICBT) for this target group. The main objectives are to establish the efficacy, cost-effectiveness, and long-term effects of the guided and self-guided ICBT for adolescents with mild to moderate depression in a randomized controlled trial (RCT) with three-arms; guided ICBT (with therapist-support) and self-guided ICBT (without therapist-support) vs treatment as usual (TAU).
Detailed description
Primary and secondary objectives
Primary objective:
- To determine the clinical efficacy of Guided and Self-guided ICBT for depression for reducing depressive symptom severity (as measured by the CDRS-R (27) in adolescents with mild and moderate major depressive disorder (MDD), compared with an active control intervention (treatment as usual within primary or secondary child and adolescent mental health care). The primary endpoint is the follow-up 3 months post-treatment.
Secondary objectives:
- To establish the 12-month durability of the treatment effects.
- To conduct a health-economic evaluation of guided ICBT for depression and self-guided ICBT for depression, compared with TAU, from multiple perspectives, both in the short term (primary endpoint) and the long term (12-month follow-up).
- To investigate potential mediators behind a potential treatment effect of ICBT.
Research questions:
- Is guided and self-guided ICBT more efficacious than TAU in regard to the reduction of depressive symptoms?
- Is guided and self-guided ICBT more cost-effective than TAU?
- Is self-guided ICBT more cost-effective than guided ICBT?
- Are the therapeutic gains of ICBT maintained long term (i.e., 1 year after the intervention)?
- Do changes in activation and avoidance (BADS) mediate changes at post-treatment in self-reported depressive symptoms (QIDS-A-17) in adolescents receiving ICBT (with or without therapist support), but not in the control group (treatment as usual)?
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 3
- Model description
- Single-blind parallel-group randomised controlled trial
| Arm | Type | Receives |
|---|---|---|
| Guided ICBT | Experimental | Behavioral: Behavioral activation (BA)Participants in guided ICBT will receive internet-delivered CBT with therapist support. The treatment consists of 8 online modules with interactive features such as videos and illustrations, delivered over a maximum of 10 weeks. The main treatment focus is behavioral activation. The adolescent and the caregiver are provided with their own separate programs and login to the treatment platform. The caregiver's program also consists of 8 chapters, including psychoeducation about depression and how to support their adolescent in treatment. The adolescents and caregivers have regular contact with a personal assigned therapist via written text messages in the platform. Participants are typically in contact with their therapist several times a week. The adolescent and caregiver can continue to access all treatment modules for the whole follow-up period (3 months), but without therapist-support. |
| Self-guided ICBT | Experimental | Behavioral: Behavioral activation (BA)The self-guided arm is identical to the guided arm, however without the therapist support. To ensure patient safety, there will be clear instructions to the patients and primary caregivers on how to get in contact with the study team in case of acute problems, and there will be clinical routines to detect and manage deterioration or suicidal tendencies. |
| Treatment as usual (TAU) | Active comparator | Other: Regular care within primary or secondary mental health care for childrenParticipants randomized to TAU, will be referred to the local CAMH's or primary care unit for children and youths and will be free to receive any treatment, either psychosocial, medical, or a combination of both. The content of TAU and the treatment techniques used will be monitored. |
Who may qualify
- Ages
- 13 to 17 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (7 listed)
- 13-17 years of age,
- A diagnosis of mild to moderate MDD based on the DSM-5,
- Willing to be randomized to either of the three treatment arms,
- Basic proficiency in Swedish, both adolescent, and a participating caregiver
- Regular access to a desktop, laptop computer connected to the internet, as well as a mobile phone,
Key exclusion criteria (5 listed)
- The presence of psychiatric problems requiring immediate treatment (e.g., high risk of suicide, psychosis, severe self-injury, bipolar disorder, clinical eating disorder, alcohol/substance abuse),
- Social problems requiring immediate action (e.g., ongoing abuse in the family, high and prolonged absence from school);
- Previous psychological treatment for MDD (CBT, interpersonal psychotherapy (IPT), or BA) for a minimum of at least 3 sessions within the last 12 months prior to assessment.
- Current use of benzodiazepines.
- Ongoing psychological treatment for any psychiatric disorder.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Behavioral activation (BA)The main goal of the BA is to increase engagement in values-based activities and decrease avoidant behaviors that serve to maintain depression. The adolescent will learn about depression, how behavioral activations works, monitor their own activities, plan and do more values-based activities and deal with obstacles to getting in touch with positive reinforcement, such as avoidance behaviors. | Behavioural | Guided ICBT, Self-guided ICBT |
| Regular care within primary or secondary mental health care for childrenRegular care (supportive therapy, waitlist, psychological treatments, drugs, or a combination of different interventions) | Other | Treatment as usual (TAU) |
Primary outcome
Change from baseline in clinician-rated depressive scores on Children's Depression Rating Scale - Revised (CDRS-R)
Time frame: week 0, week 10, at 3 and 12 months follow-up
CDRS-R is a semi-structured clinician interview, assessing level of depressive symptomatology. Total range is 17-113, with higher values representing a worse outcome.
19 secondary outcomes
Clinical Global Impression Scale - Severity (CGI-S)
Time frame: week 0, week 10, at 3 and 12 months follow-up
Clinical Global Impression - Improvement (CGI-I)
Time frame: week 10, at 3- and 12 months follow-up
Children's global assessment scale (CGAS)
Time frame: week 0, week 10, at 3 and 12 months follow-up
Internet Intervention Patient Adherence Scale (iiPAS)
Time frame: Week 10
Anhedonia Scale for Adolescents (ASA)
Time frame: week 0, week 10, at 3 and 12 months follow-up
Affective Reactivity Index (ARI)
Time frame: week 0, week 10, at 3 and 12 months follow-up
Behavioral activation of Depression Scale - short form (BADS-S)
Time frame: week 0, weekly during treatment (week 1 to week 10), at 3- and 12 months follow-up
Concomitant interventions
Time frame: Week 10 and 3- and 12-months follow-up assessments.
The Client Satisfaction Questionnaire-8 (CSQ-8) - adolescent and parent version
Time frame: week 10
Insomnia Severity Index (ISI)
Time frame: week 0, week 10, and at 3- and 12 months follow-up
Kidscreen-10 Index - adolescent and parent version
Time frame: week 0, week 10, at 3- and 12-months follow-up
Need for further treatment - adolescent and parent version
Time frame: at 3 months follow-up
Negative Effects Questionnaire (NEQ-20) - adolescent and parent version
Time frame: Week 10 and 3 months follow-up
The Revised Children's Anxiety and Depression Scale, short (RCADS-S) -adolescent and parent version
Time frame: week 0, week 10, 3- and 12 months follow-up
Quick Inventory of Depressive Symptomatology, 17 items (QIDS-17) - adolescent and parent version
Time frame: week 0, weekly from week 1 to week 10, at 3- and 12 months follow-up
Work and Social Adjustment Scale, youth version (WSAS-Y) - adolescent and parent version
Time frame: week 0, week 10, 3- and 12 months follow-up
The Expressed Emotion Adjective Checklist (EEAC)
Time frame: week 0, week 10, 3- and 12 months follow-up
Trimbos Questionnaire for Costs associated with Psychiatric Illness (TiC-P)
Time frame: week 0, week 10, at 3- and 12 months follow-up
Treatment credibility - adolescent and parent version
Time frame: week 3
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Jun 2026.
- Derived from this study: PubMed 39414268Andersson R, Vigerland S, Lenhard F, Ahlen J, Bottai M, Mataix-Cols D, Serlachius E. Single-blinded, randomised, parallel-group, controlled trial comparing the efficacy and cost-effectiveness of therapist- and self-guided internet-delivered behavioural activation versus treatment as usual for adolescents with mild to moderate depression: study protocol. BMJ Open. 2024 Oct 15;14(10):e083507. doi: 10.1136/bmjopen-2023-083507.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Eva Serlachius, PhD principal investigator
Karolinska Institutet
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Behavioral activation (BA) and Regular care within primary or secondary mental health care for children in people with Major Depressive Disorder, run by Region Stockholm at 1 site in Sweden.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 1 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Sweden. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change from baseline in clinician-rated depressive scores on Children's Depression Rating Scale - Revised (CDRS-R) (time frame: week 0, week 10, at 3 and 12 months follow-up). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04977856, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Jun 2026.