Clinical Trial Details
— Status: Active, not recruiting
Administrative data
| NCT number |
NCT05686512 |
| Other study ID # |
jaai01 |
| Secondary ID |
|
| Status |
Active, not recruiting |
| Phase |
N/A
|
| First received |
|
| Last updated |
|
| Start date |
February 13, 2023 |
| Est. completion date |
October 31, 2024 |
Study information
| Verified date |
April 2024 |
| Source |
Region Stockholm |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
Objectives: In the past ten years in Sweden, a new form of primary care units called first
line mental health (FLMH) has been implemented to improve mental health services for children
and adolescents. Using a structured and collaborative approach including experts, clinicians,
and patients, the investigators have developed a transdiagnostic psychological intervention
for anxiety based on cognitive behavioural therapy (CBT) that aims to fit the FLMH care
context. The current study aims to test the CBT intervention "Step-by-Step" in a randomized
pilot study (N=36) to explore the feasibility of the study design.
Rationale for study: Childhood anxiety is common and associated with suffering and impairment
in several life areas. CBT is an evidence-based treatment for anxiety disorders in children,
but there is a need of increasing access to treatment. Offering CBT for childhood anxiety in
primary care is a way to offer early and accessible treatment. However, there is a lack of
CBT interventions developed for and evaluated in primary care.
Prior to a properly powered randomized controlled study, evaluating efficacy of the
Step-by-Step, the investigators need to conduct a pilot study to, primarily, establish the
feasibility of the study design and trial procedures and secondarily, provide preliminary
data on acceptability and clinical efficacy.
Description:
INTRODUCTION Anxiety is the most common reason for contact with the first line mental health
(FLMH) in Sweden. Anxiety disorders are associated with negative effects in several life
areas such as school functioning, peer relationships, and family life. Anxiety disorders in
children also predict a number of adverse future events such as depression, alcohol and drug
abuse, suicide-attempts, and financial problems in young adulthood. Increasing access to
evidence-based interventions (EBIs) for child and adolescent anxiety is an urgent task.
Today, only a few children and adolescents with life-interfering anxiety use mental health
services.
CBT is a treatment that usually involves efforts to change behavioral and thinking patterns.
Numerous studies have found evidence for the efficacy of CBT in the treatment of child
anxiety, but typically, these treatment programs have been developed for use in a psychiatric
setting. The FLMH assignment focuses on early interventions (prevention and treatment)
delivered to children and adolescents (and their parents) with mild to moderate mental health
problems. A challenge for the FLMH services has been to identify EBIs for anxiety that fit
the needs of their patients and their organization, as the available EBIs almost exclusively
have been evaluated within the psychiatric domain (i.e., specialist care) rather than with
primary care in mind. To solve this problem, FLMH services sometimes offer a full-length EBI,
although it does not fit well into the primary care setting (typically the 10 session CBT
group program Cool Kids). Or, more commonly, they shorten the intervention despite that
empirical support is lacking concerning whether this can be done with maintained treatment
efficacy.
Just because an intervention is evidence-based, it does not always fit seamlessly into a
certain care setting. The context where the intervention was developed and tested often
differ in substantive ways from the context where it is applied. For instance, staff
training, resources and patient characteristics might be different. These differences between
health care contexts means that EBIs often need to be adapted to fit with the new context. In
the FLMH guidelines, CBT is the recommended intervention for child and adolescent anxiety.
However, these guidelines refer to studies of comprehensive interventions, typically
including ten or more sessions, developed for children with manifest clinical disorders.
Consequently, providing CBT within the FLMH means a dilemma concerned with the extent to
which the intervention needs to adhere to the original version and the extent to which
changes in response to resource restraints and possibilities in the local care context can be
done with maintained treatment acceptability and efficacy.
Recently, the investigators have used a structured co-creative approach to develop a CBT
intervention to the FLMH in preparation for the current project. The investigators have
conducted workshops with experts on CBT for childhood anxiety and with clinicians and heads
of three FLMH units. The investigators have also interviewed parents with experience of
participating (together with their child) in CBT for childhood anxiety. Based on this
information the investigators have developed a treatment called "Step by Step", a stepped
care approach to treat anxiety within primary care. During the past months, the investigators
have also preliminary tested the acceptability, appropriateness, and feasibility of the
Step-by-Step at one FLMH-unit, including 4 participants. Individual qualitative interviews
were conducted with therapists, participating children and caregivers after completing the
intervention. Interview data was analyzed using thematic analysis.
OBJECTIVES The overarching aim with this research project is to increase the availability to
evidence-based psychological treatments for children with anxiety treated within primary
care.
Primary Objective: To test the Step-by-Step treatment compared to Cool Kids (an
evidence-based treatment) in a randomized pilot study (N=36), to explore the feasibility of
the study design.
Secondary Objective: To provide preliminary data on acceptability and clinical efficacy.
PROJECT DESCRIPTION Control group justification: The choice of type of control condition in a
trial for a psychological intervention will depend on several factors including the disease
and its characteristics, the development phase, the purpose of the study, and the resources
available. The investigators decided on Cool Kids for the following reasons: (a) The
investigators are interested in comparing Step-by-Step to Cool Kids, to see in a future
larger trial if the Step-by-Step is non-inferior to a (comprehensive) evidence-based
treatment. (b) The Cool Kids is the most implemented treatment for childhood anxiety in
Sweden (both in primary care and in the child- and adolescent psychiatry). (c) Waitlist would
not be an ethical choice because there are efficient treatment options available for anxiety
in children.
Study Setting: The project will be located at four FLMH-units in Sweden.
Power Analysis: The aim of the study is to evaluate feasibility and acceptability. The
investigators have not made any calculation of statistical power, as the investigators do not
intend to use inferential statistics in the analyses. There will be 36 participants included,
which means three Step-by-Step groups and three Cool Kids groups. The investigators consider
this number of children to be suitable to get a broad picture of feasibility and
acceptability. The study will be conducted at different FLMH-units, which the investigators
consider important to assess the feasibility of our study design.
Data collection: Demographic information (e.g., age, sex, caregivers' educational level,
country of birth for caregivers and children) will be collected at baseline and summarized
descriptively in sample characteristics. Trial feasibility data (e.g., number of recruited
participants, completion rates of the intervention and assessments) will be collected and
summarized using descriptive statistics. Clinician-rated anxiety will be administrated by a
trained FLMH-therapist at baseline before randomization. At post intervention (defined as 12
weeks after the start of the intervention), the clinician-rated anxiety will be conducted by
a trained assessor blinded to treatment allocation. Child-and parent-rated anxiety will be
assessed at baseline and 12 weeks after the start of the intervention.
Screening and recruitment procedures: At first visit at the FLMH-unit, the caregiver(s) and
the child meet a therapist. The therapist typically collects information about the medical
history (including potential previous mental health problems) of the child, assess the
severity of mental distress and the global function of the child. If the eligibility criteria
are met, the child and caregiver(s) will receive written and verbal information about the
study and will be given opportunity to ask questions about the study. If interested in
participation, informed written consent will be obtained from all caregivers and the child.
If not eligible or interested in participation, patients will be offered regular care at the
FLMH-unit (which may include the Cool Kids program or non-manualized individual CBT). If
there is a need of contact with specialized psychiatric care and/or other organizations than
FLMH (i.e., social services or school) families will be referred according to standard
routines at the FLMH units.
Randomization, enrolment and masking: Participants will be randomised at a 1:1 ratio to
Step-by-Step or the Cool Kids. Randomisation and masking procedures will be conducted by a
researcher in the research group not involved in the clinical aspects of the study. Each
FLMH-unit will receive 12 sealed envelopes with six Step-by-Step and six Cool Kids
allocations numbered between 1-12. The investigators will use a block-randomization, with
block sizes (randomly varying) of 2 and 4. The randomization will be generated using a
computer random number generator.
Training and monitoring: All assessors/therapists will receive adequate training before the
trial starts. Assessors (i.e., all assessors at the FLMH-units and follow-up assessors) will
have received training in the PARS by the doctoral student and psychologist Albin Isaksson.
Cool Kids therapists will have received a 2-days training by Skåne certified "train the
trainers" at the Skåne child and adolescent psychiatry. Step-by-Step therapists will have
received a half day training by psychologists at Gustavsbergs health center (who have
experience from running the Step-by-Step in small-scale testing). Adherence to the treatment
manuals will be evaluated by independent assessment of a random selection of 25% of the audio
recorded sessions. Protocol violations will be recorded.
END OF TRIAL The trial will end when the final data (at the 12-week assessment) has been
collected for the final participant. Participants are free to withdraw from the study at any
point. After the withdrawal, participants will not be requested to complete any further
measures but will be asked to provide non-obligatory feedback regarding their reason for
withdrawal. This reason (if given) will be logged for reporting purposes. Withdrawn
participants will not be replaced in the trial.
Outcome measures will not be analysed until the end of the trial period and will therefore
not inform decisions to stop the research. As the research is conducted within regular
first-line operations, professional obligations and the units' routines are followed to
handle issues related to patient safety. If during assessment, during an ongoing intervention
or in connection with the end of an intervention, a need for care at a different level of
care (e.g., in the case of serious psychiatric problems) or a need for interventions from
another agency (e.g. due to abuse by a parent) emerges, exposure to violence or neglect)
participants will be referred or referred to the appropriate agency.
DATA MANAGEMENT All aspects of data management of the trial will comply with the General Data
Protection Regulation and good clinical practice.
Data collection and handling: Audio recordings will be stored on a secure server. Upon
inclusion in the pilot study, each participant is assigned an ID number that replaces name
and social security number. A code key is established to connect the participant ID and
associated data to the participant's personal data. As the study is carried out in a clinical
environment, the notes are made in medical records as standard routine. All data collection
is monitored by the responsible researcher and PhD student in the project.
BASS: BASS is the name of the data collection tool. BASS is used both for manual entry of
clinician assessed/gathered information, as well as for remote (via the internet)
administration of child- and parent-reported questionnaires. Regardless of the method above,
all data goes into the same database.
