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Smart Sensory Technology in Psychotherapy for Pediatric OCD (SSTeP-KiZ)

Primary Purpose

Obsessive-Compulsive Disorder

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Online-based Cognitive-behavioral Therapy for OCD
Sponsored by
University Hospital Tuebingen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obsessive-Compulsive Disorder focused on measuring Obsessive-compulsive Disorder, Children and Adolescents, Cognitive-behavioral therapy, Digital sensory device

Eligibility Criteria

12 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • children and adolescents with obsessive-compulsive disorders
  • aged 12 to 18 years
  • a primary DSM-5 obsessive-compulsive disorder
  • at least one primary caretaker
  • German-speaking (child & caretakers)
  • family home equipped with broadband internet connection
  • written informed consent of the child and its caretakers
  • psychiatric comorbidities will be allowed as long as the comorbid disorder does not have a higher treatment priority than OCD (i.e., psychosis, eating disorder and severe depression)
  • Medication is allowed if treatment was stable for 6 weeks before diagnostics and will then be taken during the trial.

Exclusion Criteria:

  • IQ below 70
  • patients do not speak or understand German
  • patients have a psychiatric comorbidity or suicidality that makes participation clinically inappropriate
  • too seriously ill so that they should be treated in the hospital
  • stable social environment, able to support the children adequately during therapy. - drug addiction
  • if the family seems to be severely psychologically burdened so that participation in the sessions and support of the children during the trial will not be possible
  • no other psychological treatment is allowed
  • If reporting side effects or circumstances that make iCBT treatment clinically inappropriate, or if wished by the patients, the patients are excluded from the study and transferred to another more appropriate therapy option.

Sites / Locations

  • Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Treatment with cbt

Arm Description

Treatment for 26 patients with obsessive-compulsive disorder, 14 sessions, each about 90 minutes.

Outcomes

Primary Outcome Measures

System Usability Scale (SUS) - assessment of the change in the handling of the technical equipment during treatment
Patients are to answer a total of 60 questions with 10 questions for each technical device from the system usability scale (SUS), regarding the handling of the technical equipment and to capture the change in it.
Therapy Process Questionnaire (TPQ) - assessing the stability of the therapeutic relationship and possible changes in the treatment process
Patients are to rate how they perceive the therapeutic process.
Client Satisfaction Questionnaire-8 (CSQ-8)
We assess participant's perceptions of the value of the treatment they received
Questionnaire for the evaluation of the treatment (FBB)
It records how satisfied the participants were with the treatment. We reduced the total number of questions from 20 to 17, as 3 items covered circumstances that did not occur in the context of internet-based therapy.
Change in Health Care Utilization, measured by HCU-Q (Health Care Utilization-Questionnaire)
Questionnaire to capture costs and time spent on online-based treatments; Health Care Utilization-Questionnaire, change is assessed between baseline and the last session.
Change in Quality of Life: EQ-5D-3L (European Quality of Life Five Dimensions Questionnaire)
Questionnaire to capture costs and time spent on online-based treatments: Questionnaire to capture costs and time spent on online-based treatments, measured by European Quality of Life Five Dimensions Questionnaire Three Level Version (EQ-5D-3L).
Change in costs spent on online interventions: CIIQ (Caregiver Indirect and Informal Care Cost Assessment Questionnaire)
Questionnaire to capture costs and time spent on online-based treatments: Caregiver Indirect and Informal Care Cost Assessment Questionnaire (CIIQ)
Change in affinity for technology (TA-EG)
Technology Affinity Questionnaire (TA-EG): The TA-EG can be answered by patients and their parents and contains 19 items. It measures the attitude towards and use of electronic devices.
Change in attitudes toward and satisfaction with telemedicine psychotherapy (EZtP)
Questionnaire on the Attitude and Satisfaction of Telemedicine Psychotherapy (EZtP). The EZtP is a self-developed questionnaire that measures attitudes to and satisfaction with telemedicine psychotherapy. It can be answered by both the adolescents and the parents.
Barriers to Treatment Participation Scale (BTPS)
The Barriers to Treatment Participation Scale, is a 44 item rating of how much parents agree with statements about their expectancies of barriers to treatment participation for their child, using a 5-point Likert scale (1=totally disagree, 5= totally agree).
Measures of feasibility: Manual Rating Form (MRF)
The Manual Rating Form (MRF) is used to assess feasibility of the manual.
Measures of feasibility: Summary Therapist Feedback Form (STFF)
The Summary Therapist Feedback Form (STFF) is used to assess the ease of manual implementation completed after each case.
Implementation and satisfaction questionnaire for the children
We designed an implementation and satisfaction questionnaire for the children. It covers the subject's dosage, quality, adaption, responsiveness and program differentiation.
Implementation and satisfaction questionnaire for the parents
We designed an implementation and satisfaction questionnaire for the parents. It covers the subject's dosage, quality, adaption, responsiveness and program differentiation.
Implementation and satisfaction questionnaire for the therapist
We designed an implementation and satisfaction questionnaire for the therapist. Questions regarding whether the intervention was being delivered as written (adherence) and the representativeness of the participants (reach) were implemented in the therapist's questionnaire covering questions like "The psychoeducation/relapse prophylaxis/exposure sessions were carried out as planned." and a checklist regarding information e.g. about the socioeconomic status, age, gender or IQ.

Secondary Outcome Measures

Children's Yale-Brown Obsessive Compulsive Scale (CY-BOCS)
The CY-BOCS is a clinician-administered instrument that evaluates obsessions and compulsions separately on time consumed, distress, interference, resistance, and control. A score higher than 16 describes clinical relevant obsessive-compulsive symptoms. The short form of the CY-BOCS is conducted daily on the app as part of the mobile assessment.
Children's Global Assessment Scale (CGAS)
The CGAS is a clinician's rating of the patient's overall level of functional strain.
Clinical Global Impressions-Improvement (CGI-I)
The CGI-I is used to assess overall clinical improvement based on symptoms observed and impairment reported. The clinical-rated scale has been used successfully in patients with OCD.
Clinical Global Impressions-Severity (CGI-S)
Is a clinical rating of symptom severity. The CGI-S correlates strongly with the CY-BOCS total score in pediatric OCD patients, and is widely used and has been shown to be treatment sensitive.
Children's DIPS Open Access: Diagnostic Interview in Childhood and Adolescent Mental Disorders (Kinder-DIPS)
The Kinder-DIPS is a structured clinical interview for the diagnosis of mental disorders. There is a child version and a parent version. Both, the child version and the parent version, are performed.
Brief Self-Control Scale
Patients will be given questions concerning self-control (Brief Self-Control Scale, German Version (Sproesser et al., 2011))
Self-efficacy
Patients answer questions regarding self-efficacy according to the questionnaire of Schwarzer & Jerusalem (1999).
Coping strategies
Patients answer questions regarding coping strategies according to the questionnaire of Schwarzer & Jerusalem (1999).
Self-regulation
Patients answer questions regarding self-regulation according to the questionnaire of Schwarzer & Jerusalem (1999).
Procrastination
Patients answer questions regarding procrastination according to the questionnaire of Schwarzer & Jerusalem (1999).
Child Behavior Checklist (CBCL)
The Child Behaviour Checklist (CBCL/6-18R) is used to record behavioural problems, emotional problems, somatic complaints as well as social competences of children and adolescents of school age from the parents' point of view.
Youth Self-Report (YSR)
The YSR/11-18R (youth version) was derived directly from the CBCL and allows an assessment of the largely identical characteristics from the perspective of adolescents.
Child Obsessive-Compulsive Impact Scale (COIS-RC)
The COIS-RC Culture includes a parent and a child report. It is a 33-item questionnaire designed to assess the impact of OCD symptoms on the psychosocial functioning of children and adolescent in home, social, and academic environments.
Fair Intelligence Test (CFT 20-R)
The CFT 20-R records the basic intelligence according to the general fluid ability.
Questionnaire for self-assessment of depressive disorders (DISYPS-III SBB- DES)
The SBB-DES (DYSIPS-III) is a self-report questionnaire for adolescents (11 to 18 years) and part of the Diagnostic System for Mental Disorders according to ICD-10 and DSM-5 for children and adolescents. It records the different symptoms of a depressive disorder, the extent of distress and the competencies of the adolescent.
Screen for Child Anxiety Related Emotional Disorders (SCARED)
The SCARED is a psychometrically sound child- and parent-report questionnaire which assesses the presence of DSM-IV anxiety symptoms.
Questionnaire for Measuring Health-Related Quality of Life in Children and Adolescents (KIDSCREEN)
The questionnaires can be used to assess the subjective health and well-being of children and adolescents aged 8 to 18 years. A corresponding parent version is available for parents.
Ulm Quality of Life Inventory for Parents of Chronically Ill Children (ULQUIE)
The ULQUIE was used to record the quality of life of the parents.
Affect questionnaire
The emotional state of the patients is recorded daily by the app (ambulatory assessment)

Full Information

First Posted
December 10, 2021
Last Updated
September 28, 2023
Sponsor
University Hospital Tuebingen
Collaborators
Universität Tübingen, University of Hohenheim
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1. Study Identification

Unique Protocol Identification Number
NCT05291611
Brief Title
Smart Sensory Technology in Psychotherapy for Pediatric OCD
Acronym
SSTeP-KiZ
Official Title
Smart Sensory Technology in Telepsychotherapy for the Treatment of Obsessive-compulsive Disorder in Children and Adolescents
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
August 1, 2021 (Actual)
Primary Completion Date
March 31, 2023 (Actual)
Study Completion Date
March 31, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Tuebingen
Collaborators
Universität Tübingen, University of Hohenheim

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Telemedicine interventions enable the improvement of behavioral state-of-the-art treatment of OCD, as therapy can be delivered in the patients' immediate home environment, allowing for more valid symptom actualization. In addition, access to experts is made possible even in rural areas, and the inhibition to seek therapy can be reduced. In a preliminary study, our research group was able to demonstrate the efficiency of using telemedical access. SSTeP-KiZ aims at the further development of telemedical treatment of children with OCD by using sensor technology in the home setting, where most symptoms occur. In this context, relevant emotional states of the patients such as anxiety and stress reactions shall be quantified reliably during the therapy session with exposures by combining different sensor modalities. As a result, the therapy procedure can be immediately and individually adapted to the patient and the situation, thus optimizing the success of the treatment. Methods: It is planned to establish the therapy system on a sample of 10 healthy children and 5-10 patients with OCD treated at University Hospital of Tübingen. Afterwards we will recruit 26 children with obsessive-compulsive disorder aged 12-18 years to conduct therapy with them. There are 14 weekly therapy sessions via teleconferencing with the children and parents. During the sessions and exposures, patients' field of view is recorded via eye trackers, measures of stress responses via heart rate and pupillometry, and movement measures for approach-avoidance behaviors. Using an AI approach, these indicators are integrated and reported back to the therapist online to optimize the therapy process. Accompanying app-based daily symptoms will also be collected by the children and parents and processed for use in the therapy process. We expect a good feasibility and significant symptom reduction by this therapeutic approach and the chance to make this system usable for broad clinical application.
Detailed Description
The main goal of SSTeP-KiZ is the implementation of sensors in the existing telepsychotherapeutic treatment of children and adolescents with obsessive-compulsive disorder. SSTeP-KiZ aims to significantly improve the telepsychotherapeutic treatment options for this group of patients through the use of sensors that can be worn during symptom triggering situations at home in patients' everyday lives, and an analysis and incorporation of the multimodal sensor data into the therapeutic process. In the medium term, SSTeP-KiZ should enable the use of real-time data on anxiety and stress levels (pupillometry, heart rate, eye tracking) obtained during therapy sessions by the therapist while the patient is still in the therapy session. Thus, even under the conditions of telepsychotherapy, despite the physical absence of the therapist, the individual intensity of the therapy sessions can be directly adjusted. In addition, the compliance and satisfaction of the patients during the accompanied therapy tasks can be directly promoted. Furthermore, the data obtained within the framework of SSTeP-KiZ should also be suitably prepared concerning the children and adolescents and their relatives and, in the sense of therapeutic feedback, suitably visualized to form an additional component of the therapy. Goals: A. Development of a prototype for a multisensory therapy system in healthy children and adaptation to mentally ill children with an obsessive-compulsive disorder. B. Evaluation of the prototype in the context of an internet-based psychotherapy for mentally ill children with an obsessive-compulsive disorder C: Preparations for the introduction of the multisensory therapy system into broad clinical application in the health care system Sample I: 10 healthy children: Sample II: 5-10 patients of University Hospital Tübingen with OCD. Sample III&IV: 6 & 20 children with OCD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obsessive-Compulsive Disorder
Keywords
Obsessive-compulsive Disorder, Children and Adolescents, Cognitive-behavioral therapy, Digital sensory device

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All participants will be treated with cognitive behavioural therapy during our feasibility study.
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment with cbt
Arm Type
Experimental
Arm Description
Treatment for 26 patients with obsessive-compulsive disorder, 14 sessions, each about 90 minutes.
Intervention Type
Behavioral
Intervention Name(s)
Online-based Cognitive-behavioral Therapy for OCD
Other Intervention Name(s)
Online-based Psychotherapy
Intervention Description
26 patients with obsessive-compulsive disorder (OCD) receive treatment with cognitive-behavioral therapy. 14 sessions will take place via the internet.
Primary Outcome Measure Information:
Title
System Usability Scale (SUS) - assessment of the change in the handling of the technical equipment during treatment
Description
Patients are to answer a total of 60 questions with 10 questions for each technical device from the system usability scale (SUS), regarding the handling of the technical equipment and to capture the change in it.
Time Frame
After week 1, week 7 and week 14
Title
Therapy Process Questionnaire (TPQ) - assessing the stability of the therapeutic relationship and possible changes in the treatment process
Description
Patients are to rate how they perceive the therapeutic process.
Time Frame
Weekly after each therapy session, for 14 weeks of therapy
Title
Client Satisfaction Questionnaire-8 (CSQ-8)
Description
We assess participant's perceptions of the value of the treatment they received
Time Frame
After the last session in week 14 (post treatment)
Title
Questionnaire for the evaluation of the treatment (FBB)
Description
It records how satisfied the participants were with the treatment. We reduced the total number of questions from 20 to 17, as 3 items covered circumstances that did not occur in the context of internet-based therapy.
Time Frame
After the last session in week 14 (post treatment)
Title
Change in Health Care Utilization, measured by HCU-Q (Health Care Utilization-Questionnaire)
Description
Questionnaire to capture costs and time spent on online-based treatments; Health Care Utilization-Questionnaire, change is assessed between baseline and the last session.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Change in Quality of Life: EQ-5D-3L (European Quality of Life Five Dimensions Questionnaire)
Description
Questionnaire to capture costs and time spent on online-based treatments: Questionnaire to capture costs and time spent on online-based treatments, measured by European Quality of Life Five Dimensions Questionnaire Three Level Version (EQ-5D-3L).
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Change in costs spent on online interventions: CIIQ (Caregiver Indirect and Informal Care Cost Assessment Questionnaire)
Description
Questionnaire to capture costs and time spent on online-based treatments: Caregiver Indirect and Informal Care Cost Assessment Questionnaire (CIIQ)
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Change in affinity for technology (TA-EG)
Description
Technology Affinity Questionnaire (TA-EG): The TA-EG can be answered by patients and their parents and contains 19 items. It measures the attitude towards and use of electronic devices.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Change in attitudes toward and satisfaction with telemedicine psychotherapy (EZtP)
Description
Questionnaire on the Attitude and Satisfaction of Telemedicine Psychotherapy (EZtP). The EZtP is a self-developed questionnaire that measures attitudes to and satisfaction with telemedicine psychotherapy. It can be answered by both the adolescents and the parents.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Barriers to Treatment Participation Scale (BTPS)
Description
The Barriers to Treatment Participation Scale, is a 44 item rating of how much parents agree with statements about their expectancies of barriers to treatment participation for their child, using a 5-point Likert scale (1=totally disagree, 5= totally agree).
Time Frame
Once after treatment (t1, after 14 weeks)
Title
Measures of feasibility: Manual Rating Form (MRF)
Description
The Manual Rating Form (MRF) is used to assess feasibility of the manual.
Time Frame
Once after treatment (t1, after 14 weeks)
Title
Measures of feasibility: Summary Therapist Feedback Form (STFF)
Description
The Summary Therapist Feedback Form (STFF) is used to assess the ease of manual implementation completed after each case.
Time Frame
Once after treatment (t1, after 14 weeks)
Title
Implementation and satisfaction questionnaire for the children
Description
We designed an implementation and satisfaction questionnaire for the children. It covers the subject's dosage, quality, adaption, responsiveness and program differentiation.
Time Frame
Once after treatment (t1, after 14 weeks)
Title
Implementation and satisfaction questionnaire for the parents
Description
We designed an implementation and satisfaction questionnaire for the parents. It covers the subject's dosage, quality, adaption, responsiveness and program differentiation.
Time Frame
Once after treatment (t1, after 14 weeks)
Title
Implementation and satisfaction questionnaire for the therapist
Description
We designed an implementation and satisfaction questionnaire for the therapist. Questions regarding whether the intervention was being delivered as written (adherence) and the representativeness of the participants (reach) were implemented in the therapist's questionnaire covering questions like "The psychoeducation/relapse prophylaxis/exposure sessions were carried out as planned." and a checklist regarding information e.g. about the socioeconomic status, age, gender or IQ.
Time Frame
Once after treatment (t1, after 14 weeks)
Secondary Outcome Measure Information:
Title
Children's Yale-Brown Obsessive Compulsive Scale (CY-BOCS)
Description
The CY-BOCS is a clinician-administered instrument that evaluates obsessions and compulsions separately on time consumed, distress, interference, resistance, and control. A score higher than 16 describes clinical relevant obsessive-compulsive symptoms. The short form of the CY-BOCS is conducted daily on the app as part of the mobile assessment.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Children's Global Assessment Scale (CGAS)
Description
The CGAS is a clinician's rating of the patient's overall level of functional strain.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Clinical Global Impressions-Improvement (CGI-I)
Description
The CGI-I is used to assess overall clinical improvement based on symptoms observed and impairment reported. The clinical-rated scale has been used successfully in patients with OCD.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Clinical Global Impressions-Severity (CGI-S)
Description
Is a clinical rating of symptom severity. The CGI-S correlates strongly with the CY-BOCS total score in pediatric OCD patients, and is widely used and has been shown to be treatment sensitive.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Children's DIPS Open Access: Diagnostic Interview in Childhood and Adolescent Mental Disorders (Kinder-DIPS)
Description
The Kinder-DIPS is a structured clinical interview for the diagnosis of mental disorders. There is a child version and a parent version. Both, the child version and the parent version, are performed.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Brief Self-Control Scale
Description
Patients will be given questions concerning self-control (Brief Self-Control Scale, German Version (Sproesser et al., 2011))
Time Frame
After week 1, week 7 and week 14
Title
Self-efficacy
Description
Patients answer questions regarding self-efficacy according to the questionnaire of Schwarzer & Jerusalem (1999).
Time Frame
After week 1, week 7 and week 14
Title
Coping strategies
Description
Patients answer questions regarding coping strategies according to the questionnaire of Schwarzer & Jerusalem (1999).
Time Frame
After week 1, week 7 and week 14
Title
Self-regulation
Description
Patients answer questions regarding self-regulation according to the questionnaire of Schwarzer & Jerusalem (1999).
Time Frame
After week 1, week 7 and week 14
Title
Procrastination
Description
Patients answer questions regarding procrastination according to the questionnaire of Schwarzer & Jerusalem (1999).
Time Frame
After week 1, week 7 and week 14
Title
Child Behavior Checklist (CBCL)
Description
The Child Behaviour Checklist (CBCL/6-18R) is used to record behavioural problems, emotional problems, somatic complaints as well as social competences of children and adolescents of school age from the parents' point of view.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Youth Self-Report (YSR)
Description
The YSR/11-18R (youth version) was derived directly from the CBCL and allows an assessment of the largely identical characteristics from the perspective of adolescents.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Child Obsessive-Compulsive Impact Scale (COIS-RC)
Description
The COIS-RC Culture includes a parent and a child report. It is a 33-item questionnaire designed to assess the impact of OCD symptoms on the psychosocial functioning of children and adolescent in home, social, and academic environments.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Fair Intelligence Test (CFT 20-R)
Description
The CFT 20-R records the basic intelligence according to the general fluid ability.
Time Frame
Baseline (t0) before treatment
Title
Questionnaire for self-assessment of depressive disorders (DISYPS-III SBB- DES)
Description
The SBB-DES (DYSIPS-III) is a self-report questionnaire for adolescents (11 to 18 years) and part of the Diagnostic System for Mental Disorders according to ICD-10 and DSM-5 for children and adolescents. It records the different symptoms of a depressive disorder, the extent of distress and the competencies of the adolescent.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Screen for Child Anxiety Related Emotional Disorders (SCARED)
Description
The SCARED is a psychometrically sound child- and parent-report questionnaire which assesses the presence of DSM-IV anxiety symptoms.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Questionnaire for Measuring Health-Related Quality of Life in Children and Adolescents (KIDSCREEN)
Description
The questionnaires can be used to assess the subjective health and well-being of children and adolescents aged 8 to 18 years. A corresponding parent version is available for parents.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Ulm Quality of Life Inventory for Parents of Chronically Ill Children (ULQUIE)
Description
The ULQUIE was used to record the quality of life of the parents.
Time Frame
Baseline (before treatment (t0)) and after treatment (t1, after 14 weeks)
Title
Affect questionnaire
Description
The emotional state of the patients is recorded daily by the app (ambulatory assessment)
Time Frame
Daily after each therapy session (approximately 5-10 minutes), for a time period of 14 weeks of therapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: children and adolescents with obsessive-compulsive disorders aged 12 to 18 years a primary DSM-5 obsessive-compulsive disorder at least one primary caretaker German-speaking (child & caretakers) family home equipped with broadband internet connection written informed consent of the child and its caretakers psychiatric comorbidities will be allowed as long as the comorbid disorder does not have a higher treatment priority than OCD (i.e., psychosis, eating disorder and severe depression) Medication is allowed if treatment was stable for 6 weeks before diagnostics and will then be taken during the trial. Exclusion Criteria: IQ below 70 patients do not speak or understand German patients have a psychiatric comorbidity or suicidality that makes participation clinically inappropriate too seriously ill so that they should be treated in the hospital stable social environment, able to support the children adequately during therapy. - drug addiction if the family seems to be severely psychologically burdened so that participation in the sessions and support of the children during the trial will not be possible no other psychological treatment is allowed If reporting side effects or circumstances that make iCBT treatment clinically inappropriate, or if wished by the patients, the patients are excluded from the study and transferred to another more appropriate therapy option.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Annette Conzelmann, Prof.
Organizational Affiliation
University Hospital Tübingen
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Tobias J Renner, Prof.
Organizational Affiliation
University Hospital Tübingen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy
City
Tuebingen
State/Province
Baden-Württemberg
ZIP/Postal Code
72076
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34432173
Citation
Hollmann K, Allgaier K, Hohnecker CS, Lautenbacher H, Bizu V, Nickola M, Wewetzer G, Wewetzer C, Ivarsson T, Skokauskas N, Wolters LH, Skarphedinsson G, Weidle B, de Haan E, Torp NC, Compton SN, Calvo R, Lera-Miguel S, Haigis A, Renner TJ, Conzelmann A. Internet-based cognitive behavioral therapy in children and adolescents with obsessive compulsive disorder: a feasibility study. J Neural Transm (Vienna). 2021 Sep;128(9):1445-1459. doi: 10.1007/s00702-021-02409-w. Epub 2021 Aug 25.
Results Reference
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Smart Sensory Technology in Psychotherapy for Pediatric OCD

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