Digital OC Training in Children and Adolescents
ConditionObsessive Compulsive Behavior
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age7-17
SponsorAarhus University Hospital
About this trial
The project is an interventional trial that compares digital training programs with varying levels of therapeutic contact. All participating children and adolescents will receive a digital training program following a thorough online evaluation. Additionally, parents are invited to participate in an online, supportive parenting program designed to complement the digital treatment.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
None
Trial design
Design model
Parallel
Treatments tested in this trial
Digital behavioral training
BehavioralThe program is structured into distinct sessions, through which children and adolescents are educated about obsessions and compulsions and provided with strategies for managing their symptoms. The primary objective is to equip participants with effective coping techniques. In parallel, parents are offered a supplementary treatment program designed to provide support in their involvement in the therapeutic process. Both programs are online using videos, interactive materials and assignments for both the children/youth and the parents. Both intervention arms involve the same program. The only difference is the extent of therapist contact
Treatment groups
20 Participants
are divided into 2 treatment groupsGroup A: Therapeut-assisted armActive comparator 1 intervention
Group B: Limited therapeut-assisted armActive comparator 1 intervention
Trial outcomes
Primary outcomes
1
Feasibility and acceptability
Participant retention: the number of included participants fulfilling the training program and evaluation at end of treatment, higher scores mean better
Time frame
9 weeks2
Adverse effects
Swedish short questionnaire (description) about adverse effects, 0-1, Higher scores are worse
Time frame
Session 2 (2 weeks), session 6 (6 weeks), 9 weeks3
Experienced impairment from OC symptoms, experienced change after the training program
Qualitative interviews
Time frame
baseline, 9 weeks4
Single-case study
Obsessive Compulsive Inventory (OCI/chOCI-RP), 0-2, Higher scores mean worse
Time frame
baseline, every second week (week 2, 4, 6, 8), 9 weeksSecondary outcomes
1
To evaluate whether the digital training program can change the intensity of the obsessions and compulsions
Children Yale brown Obsessive Compulsive Scale (CYBOCS), 0-4, higher scores mean worse
Time frame
baseline, 9 weeks, 3 months2
To evaluate whether the digital training program can change the intensity of the obsessions and compulsions
Obsessive Compulsive Inventory (OCI/chOCI-RP), 0-2, Higher scores mean worse
Time frame
Baseline, 9 weeks, 3 monthsLocations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Aarhus University Hospital
Lead sponsor
Department of IT and Digitalization, AUH
Collaborator
Participating municipalities in Central Region Denmark
Collaborator
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: