An interventional study of Back2School and Treatment As Usual in Anxiety Symptoms, Depressive Symptoms and Behavioral Problem, sponsored by University of Aarhus. Completed at 1 site in Denmark. Open to participants aged 7 Years to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-03-15.
Sponsored by University of Aarhus · Not applicable, Interventional, and Treatment
Among 22 studies in Depression by University of Aarhus — 2 open to participants now, 3 under way, none of them phase 3. Depression · University of Aarhus.
Among the 22 studies in Depression by University of Aarhus, this one is the 5th largest by enrollment of the 18 interventional ones, is the only one that started in 2017, is one of 18 with no phase, and was the 13th registered.
8,577 studies on the registry are indexed under Depression; 1,720 are open to participants now.
This study's enrollment of 155 is above the median of 81 across 7,063 interventional studies indexed under Depression.
Browse Depression studies →2 of the 22 studies in Depression by University of Aarhus are open now, in 1 country. Each count lists the studies.
Of the 1,088 Depression studies recruiting now, 469 (43%) set no upper age limit and 519 (48%) stop at 75 or younger; 203 take children under 18; 310 take healthy volunteers.
This study: 7 Years to 18 Years · all sexes · healthy volunteers too.
The full table on the hub →22 studies; the count open now beside each. This study's row is marked.
First in 1997; this study’s year is marked. 1 started in 2017.
Median enrollment 91 across the 18 interventional studies, 140 across the 4 observational. Of the 16 that completed or were terminated, 1 (6%) have results posted.
University of Aarhus is the lead sponsor of 1,300 studies on the registry; 189 are open to participants now.
2 of the studies in Depression by University of Aarhus that are under way reach primary completion within a year, 0 of them phase 3. Phase 3 first, then by date:
| Study | Primary completion |
|---|---|
| NCT04537195University of AarhusEffects of a Lay-led Anxiety and Depression Self-management Program for Cancer Patients | 2026-11-01 |
| NCT06920888University of AarhusIs Less More? Dosing and Sequencing Effect | 2027-06-30 |
Among the 22 studies in Depression by University of Aarhus, from their registry updates:
The main objective of this study is to examine the efficacy of a new psychological intervention, called Back2School, in helping youths with problematic school absenteeism to return to school. Furthermore, the study will examine how well this program fares against the treatment or interventions that are usually given to youths with school absenteeism (treatment as usual or TAU).
Based on previous studies we hypothesize that the Back2School intervention will be better at improving levels of school attendance as compared with treatment as usual (TAU).
Primary objective The main objective of this study is to examine the efficacy on school attendance and wellbeing of a modular trans-diagnostic CBT intervention for youths with problematic school absenteeism in a randomized controlled trial. Based on previous studies we hypothesize that the B2S intervention will show a significant difference in impact for school attendance, in favor of Back2School intervention as compared with TAU
Trial design The study is a randomized controlled superiority trial (RCT) that compares a modular trans-diagnostic CBT intervention (Back2School), treating school absenteeism in youths aged 7-17 years with treatment as usual (TAU). The design will follow a two (Back2School and TAU) by four (Time: pre, post, 3-month, and 1-year assessment) mixed between-within design.
The study is a collaboration project between Aarhus University and Aarhus Municipality, Denmark. The setting for both the B2S and TAU interventions are within Aarhus municipality. The Back2School intervention is organized and conducted by the University Clinic, at Aarhus University. Treatment as usual interventions are organized and conducted by Aarhus Municipality.
There are considerable negative long-term consequences related to youths with school absenteeism. If the B2S intervention proves to be effective in reducing school absenteeism, it could be implemented in other municipalities in Denmark, and help to systematically treat and help youths with school absenteeism. This could possibly reduce both personal and societal costs significantly
8,577 studies on the registry are indexed under Depression; 1,720 are open to participants now.
This study's enrollment of 155 is above the median of 81 across 7,063 interventional studies indexed under Depression.
Browse Depression studies →University of Aarhus is the lead sponsor of 1,300 studies on the registry; 189 are open to participants now.
Compared within Depression, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Anxiety Disorders. The counts are of registry records indexed under each term, refreshed daily. How we classify →
Inclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
The Back2School condition is a Modular Trans-Diagnostic Cognitive Behavioral Therapy (MTCBT) treating school absenteeism in youths. The MTCBT intervention consist of 10 sessions and 4 school meetings, conducted over a period of 4 months.
Behavioral: Back2School
The Treatment As Usual condition (TAU) consist of an array of interventions that the municipality is required to give youths presenting school absenteeism. The TAU condition will last for 4 months.
Other: Treatment As Usual
Modular Trans-diagnostic Cognitive Behavioral Therapy treating school absenteeism in youths
Also known as: B2S
Aarhus municipality's treatment as usual for youths presenting school absenteeism
Also known as: TAU
Change in School Attendance - Registry data
Aarhus Municipality's registry data of the youths' school attendance
Time frame: Baseline, post-treatment (4-months), 3-months follow-up, 12-months follow-up
Change in School Attendance - Self-reported data
Self-reported school attendance in the previous two weeks, reported by parents.
Time frame: Baseline, post-treatment (4-months), 3-months follow-up, 12-months follow-up
The Strength and Difficulties Questionnaire (SDQ)
The SDQ measures psychopathology in youths (3-16 years). There is a SDQ version for youths (SDQ), parents (SDQ-P), and teachers (SDQ-T). The different versions consist of the same items, and are scored identically. Total of 25 items, rated on a 3-point scale (0-2), divided into 5 sub-scales consisting of 5 items. Sub-scales: Emotional symptoms, Conduct problems, Hyperactivity/inattention, Peer relationships problems, Pro-social behavior For each sub-scale, minimum score is 0 and maximum total score is 10 The total score is computed by summing up the sub-scales, with the exception of the "pro-social behavior" sub-scale. Minimum total score is 0, and maximum total score is 40. The extended version of the SDQ includes an impact scale with additional 8 items, regarding child distress and interference. The Impact scale is scored on a 4-point scale (0-3). The impact scale is summed up by counting only scores of 2 or 3. Minimum score 0, and maximum score 24.
Time frame: Baseline, post-treatment (4-months), 3-months follow-up, 12-months follow-up
The Spence Children's Anxiety Scale (SCAS)
Self-report rating scale assessing youths symptoms of anxiety, rated by youths (SCAS) and parents (SCAS-P). Total of 38 items, rated on a 4-point scale (0-3), divided into 6 sub-scales. The SCAS includes 6 positive filler items not included in the computation of sub-scores or total score. Sub-scales: Social Phobia (6 items), Panic disorder and agoraphobia (9 items), Generalized anxiety disorder (6 items, range 0-18), Obsessive-compulsive disorder (6 items, range 0-18), separation anxiety disorder (6 items, range 0-18), Fear of physical injury (5 items, , range 0-15). Minimum total score is 0, and maximum total score is 114. The SCAS-P is identical to the SCAS in form an scoring, but does not include the 6 positive filler items.
Time frame: Baseline, post-treatment (4-months), 3-months follow-up, 12-months follow-up
The Mood and Feelings Questionnaire (MFQ)
Covers a broad range of cognitive and vegetative symptoms of depression in youths. There is both a youth (MFQ) and parent (MFQ-P) version of the MFQ. The MFQ consistTotal of 33 items, rated on a 3-point scale (0-2). The MFQ-P consist of 34 items. Both the scores for MFQ and MFQ-P are computed by summing up all items. Higher scores indicating more sever depressive symptoms. Minimum MFQ score is 0, maximum score is 66. Minimum MFQ-P score is 0, maximum score is 68.
Time frame: Baseline, post-treatment (4-months), 3-months follow-up, 12-months follow-up
The Child Health Utility 9D Index (CHU-9D)
Designed to determine how health affect youths's lives, rated by youths. Consist of 9 items, rated on a 5-point scale. Each item is related to a dimension to how the youths are feeling worried, sad, pain, tired, annoyed, schoolwork/ homework, sleep, daily routine, and participating in activities. Higher scores for each item is related to a higher perceived difficulty related to a dimension. Each dimension/item has a minimum score of 1, and a maximum score of 5.
Time frame: Baseline, post-treatment (4-months), 3-months follow-up, 12-months follow-up
The Self-efficacy Questionnaire for School Situations (SEQ-SS)
Measures self-efficacy expectations to different school situations, rated by youths. Consist of 12 items, rated on a 5-point scale (1-5), and divided into 2 sub-scales both consisting of 6 items. Minimum SEQ-SS score is 12, maximum score is 60. Higher scores reflect greater self-efficacy expectations.
Time frame: Baseline, post-treatment (4-months), 3-months follow-up, 12-months follow-up
Self-Efficacy Questionnaire for Responding to School Attendance Problems (SEQ-RSAP)
Measures parents self-efficacy expectations to different school situations, rated by parents. Consist of 13 items, rated on a 4-point scale (1-4). Minimum score is 13, and maximum score is 52. Higher scores reflect greater self-efficacy expectations in parents ability to help their child in different school situations.
Time frame: Baseline, post-treatment (4-months), 3-months follow-up, 12-months follow-up
The Family Assessment Device (FAD)
Assess different dimensions of family function, rated by youths (12 years and older) and parents. Only the sub-scale regarding General Function is used in this study. The sub-scale consist of 12 items, rated on a 4 point-scale (1-4). The FAD is scored by calculating the mean scores of all items. Higher means are related to a more unhealthy or non-functional family function.
Time frame: Baseline, post-treatment (4-months), 3-months follow-up, 12-months follow-up
The Experience of Service Questionnaire (ESQ)
Assess the satisfaction with the treatment, rated by youths and parents. The treatment satisfaction for the youths consist of 7 items rated on a 3 point-scale (0-2), with 1 open question. Treatment satisfaction for parents is assessed using 10 items, rated on a 3-point-scale (0-2), with 3 open questions. Higher scores is associated with
Time frame: Post-treatment (4-months), 3-months follow-up.
Collaboration with the school
Assess the collaboration between the family and the school/teacher. Consist of 3 items rated on a 4-point scale (1-4). Higher scores are related to a good relationship and collaboration with the school. Both parents and teachers respond to this questionnaire.
Time frame: Post-treatment (4-months), 3-months follow-up, 12-months follow-up
This study is completed, as verified in Apr 2019. You cannot join it, but the record below documents what was studied.
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