An interventional study of Psychotherapy: 1. cognitive therapy 2.family intervention in ADHD - Combined Type, sponsored by Behandlingsskolerne. Status unknown at 1 site in Denmark. Open to participants aged 6 Years to 18 Years. Per ClinicalTrials.gov, last updated 2017-10-24.
Sponsored by Behandlingsskolerne · Not applicable, Interventional, and Treatment
Evaluating interventions for children/adolescents with Attention Deficit Hyperactivity Disorder (ADHD) is a field that offers many challenges. Even though psychotherapeutic treatment for ADHD is recommended as the first choice in many countries(1), the evidence base for this is inconsistent and outcome specific (2). For instance, parent training may not have significant effects on the core Symptoms of ADHD (3). However, trials suggest that it facilitates skills in other areas. One area where it is of potential value is social functioning (4). The randomized controlled trial (RCT)described here will test the therapeutic value of a package of psychological interventions designed to target social functioning for children and adolescents with ADHD. It will be conducted in a special school environment designed specifically for children with severe behavioral problems. Therefore, routine provision is already substantial. As a result, it was not possible to include a "no intervention group" (control group) for ethical reasons. Therefore, the value of social skills intervention was examined by comparing different "doses" of the routine intervention by testing a usual provision (UP) group against an enriched/need-based (ENP) form of provision.
Background:
In 2013, the former Danish minister of Social Affairs presented a national plan for the help and treatment of people with ADHD. Acknowledging the rise in the number of citizens in Denmark with an ADHD diagnosis, the Danish government supported an enhanced effort to offer this group adequate treatment. The government's aim was to secure an increased quality of life for individuals with ADHD.
The Ministry of Social Affairs sees ADHD as a cluster of co-occurring difficulties that creates various problems in life for affected individuals. The main goal with the national plan, was (i) to provide early years help for children, (ii) to prevent the development of ADHD type of problems, and (iii) to provide the proper treatment for people, who already have ADHD.
The plan did not consider the biological perspectives, and medicinal treatment is not mentioned as a part of the plan - while non-pharmacological interventions, such as parent training, were considered the first priority (5). This priority for non-pharmacological interventions rested partly on ethical considerations, although the report suggests that a number of training programs are evidence-based. The evidence-base for non-pharmacological interventions remains complex. For instance, the benefits of parent training and child-focused treatments for core ADHD symptom control is limited - especially when blinded outcomes are considered (6). In contrast, parent training seems to improve parenting and reduce conduct disorder (7). Social skills training may also have value (8). This is important as, although behavioral problems are not considered a core symptom in ADHD, social functioning deficits are recognized in many children with ADHD (9) and conduct disorder is a relatively common comorbidity (10).
In a society like Denmark, where people with ADHD receive psychosocial treatment and support from the Social Services before they are considered for medical treatment, it is vital that studies of nonpharmacological interventions are conducted. The investigators have to analyze to what extend the interventions can have an effect and on which areas of functioning we can expect improvement. In Denmark, children with most severe behavior problems are treated in special educational settings. In these settings, nonpharmacological treatment is the norm. Considering this, more studies should be conducted in such settings to see if the approaches used are of value.
The proposed RCT will contribute to the knowledge about the value of nonpharmacological interventions, especially with regard to social functioning and skills for ADHD, by investigating treatment in a special school setting providing care for children/adolescents with severe ADHD symptoms and behavior problems.
Aims and objectives:
The overall aim of this study is to evaluate the benefits of enriching and extending an existing non-pharmacological intervention for social skills deficits in ADHD currently delivered in a special school environment. To do this, we will compare usual provision (UP) with an enhanced and need based provision (ENP).
The main research questions are:
Method:
For ethical reasons, it is not possible in this study to have a control group that does not receive treatment. The Ministry of Social Affairs legislation does not allow students to be in a control group with no treatment in a special school setting. Due to these circumstances, the study will be a pragmatic RCT study. Therefore, a two-arm RCT will be carried out to evaluate whether the effectiveness of the intervention is greater when delivered in an "enriched/need Based provision" (ENP) format compared to a "usual provision" (UP).
Study setting:
Participants will be enlisted at the three schools in Denmark; Pilelygaard, Pilen and Kompasset - each part of an organization called Behandlingsskolerne which has approximately 100 students enrolled at any time. Daily treatment is primarily offered in a school setting, but can take place elsewhere (visiting a café, walk in the park etc.). Family work will be carried out in the student´s home or at school meetings. Students in these schools do not have ASD as a primary diagnosis or a very low IQ. However, the level of comorbidity is high. More than half of the students have more than one diagnosis.
The level of staffing is high with 1:2 staff to student ratio. Many of the staff are trained to deliver psychological treatment. Both teachers and social workers are all trained in a cognitive approach and follow the guidelines of specialized psychologists in the treatment. The staff are supervised on a regular basis and participate in meetings with the school unit, class team, and the psychologists to secure every student´s progress.
Participants:
Participants in the study are all students enlisted at Behandlingsskolerne. An Organization that houses several special schools.
Inclusion criteria:
Exclusion criteria:
Recruitment:
Following the Ministry of Social Affairs legislation, students with ADHD are offered private treatment in special schools when education and treatment is not possible in public schools. Each student is individually evaluated by Social Service officials before being offered private treatment. When the student´s parents and the Social Service Department first consider Behandlingsskolerne as an option, the student´s files are send to the school and a meeting is held between the parents, officials and the school. Taking into consideration the diagnosis, the school history and recommendations from the family, the student is placed in a school unit within the organization - one that is judged able to meet the student´s unique needs. The study will consider each student enlisted in these three school units between the dates 01.03.17 and 01.09.18. Students meeting the inclusion and exclusion criteria will be take part in the study.
Intervention:
The intervention in this RCT consist of two versions of a package of psychotherapeutic sessions given to the students and students' parents. Trained psychologists offer a number of sessions in which problems regarding ADHD and/or behavioral problems are addressed. The following describes the standard interventions offered at Behandlingsskolerne for children with ADHD and severe behavioral problems (The content of the therapeutic approach is available from the author):
Intervention with students:
Interventions with parents:
The difference between the UP and ENP groups: The UP-group receives a fixed amount of intervention = five sessions (three for the student and two for the parents) each month in which relevant treatment is picked from the intervention approaches mentioned above. The ENP-group receives the same treatment options from the intervention list but in an enhanced form. This group receives not less than seven sessions (four for the student and three for the parents). Furthermore, in the ENP-Group, there is no limit regarding the number of interventions. The psychologist will evaluate how many sessions he considers are needed to progress in each case.
The psychologists will report the progress in treatment for the students in the study at monthly meetings. They track the therapy sessions offered for each student in a registration sheet. At these meetings, the ethical perspectives are discussed and the extent of the treatment is considered. If a student is not making progress, or even getting worse, a shift from the UP group to the ENP-Group is possible.
Study measures:
Diagnostic assessment:
A psychiatric assessment has been performed on every student in the study in a hospital in Denmark. These took into account the typical range of information required from an assessment from multiple sources and across multiple settings. Considering the medical history, diagnostic interviews, and test results, all students participating are diagnosed with Attention Deficit Hyperactivity Disorder (ADHD) and not ASD or with an IQ of less than 70. Behavioral problems are diagnosed in the hospital or described in the school records.
Outcomes T1 to T4 outcomes were measured using the following scales.
Social skills (primary outcome)
ADHD symptoms and conduct problems (secondary outcomes)
Statistical analysis and sample size:
The primary analysis will employ an ITT analysis, with multiple imputation of missing data, using linear mixed models to compare the two trial arms on an aggregate score on the two social skills scales at T2. T1 scores will be included in the model as a covariate. Secondary analysis will use similar models for other outcomes at other time-points. To obtain adequate statistical power, the two treatment arms will be split equally using a 1-to-1 ratio. Clinically valuable change (MIREDIF) on the primary outcome requires a minimum 15 scale point improvement which is equivalent to a .6 standard deviation change. This require 32 Students (16 in the Study Group and 16 in the Control Group) to obtain a power of 80% (100% - errors of type II) using a conventional statistical level of significance of 5%. The group will be stratified for sex of participant and by which unit they are attending.
Moderator Analysis: We will record the nature of all treatment (including medication) received, and this will be summarized and quantified and used as a moderator in the analysis.
Ethical approval and Informed consent:
Standard ethical procedures will apply. Students and participants will give written informed consent. We are obliged to protect all data collected and the data can only be used in an anonymous form. Associate Professor Henrik Skovlund from University of Århus is responsible for monitoring and securing all the ethical aspects of the study.
Allocation and blinding:
Participants in the study are allocated to each arm by using randomization system. After determining which of the three school Units the student will attend, the participants are distributed in to one of the two arms at each school (UP \& ENP).
It is not possible to fully blind parents and students as they have to give informed consent. Teachers and social workers will be kept blind to allocation as far as possible . They are not directly involved in the treatment measured in this study, even though they play a great part in it. The blindness of the teachers and social workers is important as they will be providing the ratings used in the analyses.
1,817 studies on the registry are indexed under Attention Deficit Disorder with Hyperactivity; 296 are open to participants now.
This study's planned enrollment of 32 is below the median of 71 across 1,437 interventional studies indexed under Attention Deficit Disorder with Hyperactivity.
Browse Attention Deficit Disorder with Hyperactivity studies →This is the only study on the registry with Behandlingsskolerne as lead sponsor.
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Exclusion Criteria:
Usual Provision Psychotherapy: 1. cognitive therapy 2.family intervention
Behavioral: Psychotherapy: 1. cognitive therapy 2.family intervention
Enhanced/need-based Provision Psychotherapy: 1.cognitive therapy 2.family intervention
Behavioral: Psychotherapy: 1. cognitive therapy 2.family intervention
Psychotherapy delivered by trained psychologist for the student and the student´s parents
Total score Adaptive Behavior Assesment System (ABASII)
Primary outcome will be an aggregate score on social and adaptive functioning from the assessment using ABASII (Adaptive Behavior Assessment System). The score is shown as "General Adaptive Composite" (GAC) on a scale from 60 to 140. The Mean area of GAC is found on the scale between a score 90 and 109. A GAC score from 100-140 is indicating a functionning level ranging from "better than mean" to "extremely high". A GAC score from 90-60 is indicating a functioning level ranging from "below mean" to " extremly low".
Time frame: 0-12 month
Total score Social Responsiveness Scale (SRS)
Primary outcome will be an aggregate score on social functioning from the assessment using SRS (Social Responsiveness Scale). The score is shown as "T-Score" on a scale from 30 to 90. A T-Score below 60 indicates normal functioning in social responsiveness. A T-score between 60 and 75 indicates difficulties in a mild to moderate level. A T-Score higher than 75 indicates severe difficulties.
Time frame: 0-12 month
Subscale scores Strength and Difficulties Questionnaire (SDQ) on "behavioral difficulties", "getting along with other children" and "hyperactivity and concentration difficulties".
Secondary outcome will be using subscale scores of strength and difficulties using SDQ (Strength and Difficulties Qustionnaire). The SDQ has 25 items on an ordinal scale: 1. Not true 2. Partly true 3. True Each Item is scored in a range from 0-10 indicating the level of difficulties.
Time frame: 0-12 month
Total score Attention Deficit Hyperactivity Disorder Rating Scale (ADHD-RS)
Secondary outcome will be a an aggregate score of ADHD symptoms and conduct disorder using ADHD-RS (Attention Deficit Hyperactivity Disorder Rating Scale). ADHD-RS has 26 items on an ordinal scale: 1. Rarely/Never 2. Sometimes 3. Often 4. Very often The score is ranging from 0- 78 indicating the level of difficulties.
Time frame: 0-12 month
Plan to share: No
Started Mar 2016 (actual). Primary completion is estimated for Sep 2019, 42 months after the start.
Of 479 non-industry interventional studies with no phase under Attention Deficit Disorder with Hyperactivity, half reached primary completion within 24 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 43. This study's planned 42 months is above that.
Counting every sponsor, half of 510 studies reached it within 23 months; a quarter within 11 and three quarters within 41.
How these figures are worked out, and which studies are left out of them.
This study is status unknown, as verified in Oct 2017. You cannot join it, but the record below documents what was studied.
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