Add-on Therapy With Edupression.Com® on Therapy Resistant Depressive Patients Treated With Nasal Esketamine Spray (Esketamin+)
Primary Purpose
Major Depressive Disorder, Therapy Resistant Depression
Status
Recruiting
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
edupression.com®
Esketamine nasal spray
Sponsored by
About this trial
This is an interventional treatment trial for Major Depressive Disorder focused on measuring Depression, Esketamine, Treatment resistant depression, Internet-based intervention, Telemedicine
Eligibility Criteria
Inclusion Criteria:
- Age 18 or older
- Initial MADRS-Score of 22 or above
- Diagnosis of a therapy-resistant depression following the definition of the European Medicines Agency (EMA) - absence of remission after two or more guideline-oriented therapies
- Patients assigned to treatment with nasal esketamine spray Spravato®
- Signed informed consent
- Native German speaker
- Basic knowledge in using computers/smartphones operationalized as daily use of at least two devices (such as tablets, computers, smartphones etc)
Exclusion Criteria:
- Contraindication regarding the use of Spravato®
- Diagnosis of one of the following psychiatric comorbidities: substance abuse, schizoaffective disorders, schizophrenia, bipolar disorder, organic disorders diagnosed via Mini International Neuropsychiatric Interview (MINI)
Sites / Locations
- Medical University ViennaRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
edupression.com® + treatment-as-usual
treatment-as-usual
Arm Description
Patients are receiving treatment with edupression.com® in addition to TAU (treatment-as-usual) with esketamine nasal spray
Patients are receiving TAU (treatment-as-usual) with esketamine nasal spray
Outcomes
Primary Outcome Measures
Therapy response (observer-rated)
Change in depressive symptoms according to MADRS-Score (0-60 points, higher values stand for)
Percentage of received esketamine treatments in relation to scheduled ones
Change in therapy adherence according to a percentual increase of received esketamine treatments in accordance to scheduled ones
Secondary Outcome Measures
Therapy response (self-rated)
Change in depressive symptoms according to the self rating scale PHQ-9 (Patient Health Questionnaire-9) (1-27 points, higher values stand for increased severity)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04843462
Brief Title
Add-on Therapy With Edupression.Com® on Therapy Resistant Depressive Patients Treated With Nasal Esketamine Spray
Acronym
Esketamin+
Official Title
A Randomized, Controlled Pragmatic Trial Assessing the Value of an add-on Therapy With Edupression.Com® in Therapy Resistant Depressive Patients Treated With Esketamine Nasal Spray
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 29, 2021 (Actual)
Primary Completion Date
April 14, 2023 (Anticipated)
Study Completion Date
April 14, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Lukas Pezawas
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Pragmatic clinical trial of an add-on therapy regarding the use of edupression.com® - a licensed computer based self-help program - on patients with therapy-resistant depression receiving esketamine nasal spray
Detailed Description
edupression.com® - is a medical product and computer based self-help program based on cognitive behavioral therapy, psychoeducation and mood tracking. Patients included in the interventional arm of this study are receiving full access to edupression.com®.
Due to limited resources regarding face-to-face therapy and a high prevalence of Major Depressive Disorder - of which 37% can be identified as therapy-resistant depression (TRD) according to the definition of the European Medical Agency (EMA) - low-intensity psychosocial interventions such as edupression.com® are recommended as first-line digital therapeutic agent by international guidelines such as National Institute for Health and Care Excellence (NICE) guidelines. Studies have shown that digital interventions - such as edupression.com - show comparable clinical efficiency to face-to-face therapy and therefore could be able to fill the gap in limited ressources. In this study patients with therapy-resistant depression are receiving therapy with edupression.com® in addition to their treatment-as-usual with esketamine nasal spray. Comparable studies have shown that patients receiving psychotherapy in addition to their medical therapy benefit in regards to their clinical outcome. Considering these findings, this study is aimed to investigate potential clinical benefits in patients receiving digital therapy with edupression®.com as an add-on therapy to their treatment-as-usual therapy with esketamine nasal spray.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder, Therapy Resistant Depression
Keywords
Depression, Esketamine, Treatment resistant depression, Internet-based intervention, Telemedicine
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The interventional study consists of two parallel study arms. The interventional group receives "treatment-as-usual" with nasal esketamine spray and access to edupression.com®. The control group only receives "treatment-as-usual".
Masking
Participant
Masking Description
Data will be immediately pseudonymized and stored as a master list at the internal server of the MUV (Medical University Vienna). The study staff will only have access to the master list and only the principal investigator and study director will have access to the pseudonymization list. This locked place will be located at the clinic (MUV). All non-personal pseudonymized research relevant data are stored in a master list on a server of the research group at the MUV, to which study staff has access.
Allocation
Randomized
Enrollment
70 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
edupression.com® + treatment-as-usual
Arm Type
Experimental
Arm Description
Patients are receiving treatment with edupression.com® in addition to TAU (treatment-as-usual) with esketamine nasal spray
Arm Title
treatment-as-usual
Arm Type
Active Comparator
Arm Description
Patients are receiving TAU (treatment-as-usual) with esketamine nasal spray
Intervention Type
Device
Intervention Name(s)
edupression.com®
Intervention Description
Edupression.com® is an evidence-based self-help program that was developed for the treatment of mild to moderate unipolar depression. It is based on two core foundations, psychoeducation with elements of cognitive behavior therapy (CBT) and a mood chart. Both foundations are registered as a medical product. As such, detailed risk management documentation includes probability and severity of adverse events. Moreover, detailed strategies such as warnings were implemented in the software and documented accordingly.
It can be used on a PC as well as on mobile devices (browser, app) at any time.
Intervention Type
Drug
Intervention Name(s)
Esketamine nasal spray
Intervention Description
All patients included in this study are receiving esketamine nasal spray as treatment-as-usual
Primary Outcome Measure Information:
Title
Therapy response (observer-rated)
Description
Change in depressive symptoms according to MADRS-Score (0-60 points, higher values stand for)
Time Frame
At week 4, 8 and 12 after baseline
Title
Percentage of received esketamine treatments in relation to scheduled ones
Description
Change in therapy adherence according to a percentual increase of received esketamine treatments in accordance to scheduled ones
Time Frame
Percentage of received esketamine treatments in relation to scheduled ones after 12 weeks
Secondary Outcome Measure Information:
Title
Therapy response (self-rated)
Description
Change in depressive symptoms according to the self rating scale PHQ-9 (Patient Health Questionnaire-9) (1-27 points, higher values stand for increased severity)
Time Frame
At week 4, 8 and 12 after baseline
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 18 or older
Initial MADRS-Score of 22 or above
Diagnosis of a therapy-resistant depression following the definition of the European Medicines Agency (EMA) - absence of remission after two or more guideline-oriented therapies
Patients assigned to treatment with nasal esketamine spray Spravato®
Signed informed consent
Native German speaker
Basic knowledge in using computers/smartphones operationalized as daily use of at least two devices (such as tablets, computers, smartphones etc)
Exclusion Criteria:
Contraindication regarding the use of Spravato®
Diagnosis of one of the following psychiatric comorbidities: substance abuse, schizoaffective disorders, schizophrenia, bipolar disorder, organic disorders diagnosed via Mini International Neuropsychiatric Interview (MINI)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lukas M Pezawas, MD, Prof.
Phone
004314040035470
Email
lukas.pezawas@meduniwien.ac.at
First Name & Middle Initial & Last Name or Official Title & Degree
Gabriele Fischer, MD, Prof.
Phone
004314040035470
Email
gabriele.fischer@meduniwien.ac.at
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Markus Dold, MD., Priv.Doz.
Organizational Affiliation
Medical University of Vienna
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Gabriele Fischer, MD, Prof.
Organizational Affiliation
Medical University of Vienna
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Lukas M Pezawas, MD, Prof.
Organizational Affiliation
Medical University of Vienna
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical University Vienna
City
Vienna
ZIP/Postal Code
1090
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lukas M Pezawas, Prof.
Email
lukas.pezawas@meduniwien.ac.at
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
22132433
Citation
National Collaborating Centre for Mental Health (UK). Depression: The Treatment and Management of Depression in Adults (Updated Edition). Leicester (UK): British Psychological Society; 2010. Available from http://www.ncbi.nlm.nih.gov/books/NBK63748/
Results Reference
result
PubMed Identifier
32775969
Citation
Luo C, Sanger N, Singhal N, Pattrick K, Shams I, Shahid H, Hoang P, Schmidt J, Lee J, Haber S, Puckering M, Buchanan N, Lee P, Ng K, Sun S, Kheyson S, Chung DC, Sanger S, Thabane L, Samaan Z. A comparison of electronically-delivered and face to face cognitive behavioural therapies in depressive disorders: A systematic review and meta-analysis. EClinicalMedicine. 2020 Jun 27;24:100442. doi: 10.1016/j.eclinm.2020.100442. eCollection 2020 Jul. Erratum In: EClinicalMedicine. 2021 Nov 02;41:101182.
Results Reference
result
Learn more about this trial
Add-on Therapy With Edupression.Com® on Therapy Resistant Depressive Patients Treated With Nasal Esketamine Spray
We'll reach out to this number within 24 hrs