- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04352010
Therapy Online Plus (TOP+) - Comparing Two Online Interventions for Dealing With Challenging Life Circumstances (TOP+)
Therapy Online Plus (TOP+) - Comparing Two Online Interventions ("REMOTION" Resp. "Res-Up!") for Dealing With Challenging Life Circumstances
Psychotherapy interventions can roughly be grouped into compensation-oriented strategies (compensating for and and modifying personal deficits of patients) versus capitalization-oriented strategies (building on patients' personal strengths). Improvement of emotion regulation (compensation-oriented) as well as the activation of resilience (capitalisation-oriented) have been identified as important transdiagnostic factors in the treatment of mental disorders. The study aims to compare compensation vs. capitalization strategies by using two online programs, centered either on emotion-regulation ("REMOTION") or on activating resilience ("Res-Up!"). Res-Up! and REMOTION are administered as stand-alone intervention or as add-on treatment to standard psychotherapy.
Participants will be randomly assigned to three study conditions (Res-Up!, REMOTION, waiting control group). Outcomes are assessed at baseline, after six weeks and after twelve weeks.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Leonie F Trimpop, M.Sc.
- Phone Number: +(0)49 2302 926 9704
- Email: leonie.trimpop@uni-wh.de
Study Locations
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North Rhine-Westphalia
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Witten, North Rhine-Westphalia, Germany, 58455
- Recruiting
- Witten/Herdecke University
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Contact:
- Leonie F Trimpop, M.Sc.
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Diagnosis of a mental disorder according to DSM-5
- Recruited at the training centers of the German Association for Behavior Therapy (Deutsche Gesellschaft für Verhaltenstherapie, DGVT) at Muenster, Bielefeld and Dortmund or at the Center of Mental Health and Psychotherapy, Witten/Herdecke University (all outpatients clinics
Exclusion Criteria:
- Insufficient German language skills
- Current severe episode of major depression
- Psychotic disorder
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Online-Intervention "Res-Up!"
Participants in the Res-Up! group get access to Res-Up! while waiting for psychotherapy or in addition to psychotherapy.
Participants will answer questionnaires after inclusion as well as six and twelve weeks later.
|
Res-Up! is an internet-based intervention focusing on patients' strengths and positive experiences that have effects on distress, protective factors and quality of life.
The intervention is based on the Personal Model of Resilience (PMR; Padesky and Mooney, 2012), which is a positive intervention that utilizes patients' strengths to overcome problems.The PMR activates resilient emotions, thoughts, metaphors, images and behaviors in four steps during five sessions about the aquisition of resilient strategies and their use in daily life.
A variety of elements based on different psychotherapy approaches (Cognitive Behavioral Therapy, Emotion Focused Therapy, Positive Therapy etc.) are integrated in the program.
Participants should work through one module per week.
The intervention is conducted as I-CBT via the platform Minddistrict.Res-Up! is administered as a standalone or an add-on treatment to psychotherapy.
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Experimental: Online-Intervention "REMOTION"
Participants in the REMOTION group get access to REMOTION while waiting for psychotherapy or in addition to psychotherapy.
Participants will answer questionnaires after inclusion as well as six and twelve weeks later.
|
REMOTION is an internet-based intervention aimed at transdiagnostically reducing symptom severity and improving emotion regulation of psychotherapy patients.
The structure of REMOTION is based on the idea of an extended process model of emotion regulation as postulated by J.J. Gross (2015).
The program includes the following modules: introduction, psychoeducation, identification, selection, implementation and modification.
A variety of elements based on different psychotherapy approaches (Cognitive Behavioral Therapy, Emotion Focused Therapy, Dialectical Behavior Therapy etc.) are integrated in the program.
Participants should work through one module per week.
REMOTION is administered as a standalone or an add-on treatment to psychotherapy.
|
Experimental: Wait-control group
Participants in the wait-control group will not get access to the online-tools while waiting for psychotherapy or while in psychotherapy.
Participants will answer questionnaires after inclusion, six weeks later and twelve weeks later.They get access to one of the online-tools after 12 weeks.
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In the waiting control group participants will answer questionnaires and they will gain access to either REMOTION or Res-Up! after twelve weeks.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change on Brief Symptom Inventory - short form (BSI-18) over multiple time points
Time Frame: Change from Baseline, then after six weeks and after twelve weeks
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Franke, 2000; Internationally used self-report of symptom severity of patients [18 items] that includes three symptom scales, each including six items: Somatization, Depression, and Anxiety.
Each measured on a 5-point scale according to how much one has been bothered by the symptom in the prior week.
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Change from Baseline, then after six weeks and after twelve weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change on Patient Health Questionnaire-9 (PHQ-9) over multiple time points
Time Frame: Baseline, then after six weeks and after twelve weeks
|
Kroenke, Spitzer, & Williams, 2001; Internationally used self-report for screening, diagnosing, monitoring and measuring the severity of depression [9 items, 4-point scale ("not at all" to "nearly every day")].
It is the major depressive disorder module of the full PHQ.
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Baseline, then after six weeks and after twelve weeks
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Change on Witten Resource Questionnaire (WIRF) over multiple time points
Time Frame: Change from Baseline, then after six weeks and after twelve weeks
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Schürmann et al., 2019; Self-report of personal and external resources [37 items, 6-point Likert scale ("strongly disagree" to "strongly agree")].
Resources are measured in the three contexts: "everyday life", "crises well coped with" and "current problems" each including three subscales (action regulation, relaxation and social support).
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Change from Baseline, then after six weeks and after twelve weeks
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Change on Rosenberg-Self-Esteem Scale (RSES) over multiple time points
Time Frame: Change from Baseline, then after six weeks and after twelve weeks
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Ferring & Filipp, 1996; Self-report of general self-esteem [10 items, 4-point scale ("strongly disagree" to "strongly agree")].
A total score will be computed with summed item scores (range: 0-30).
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Change from Baseline, then after six weeks and after twelve weeks
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Change on Connor-Davidson Resilience Scale (CD-RISC-10) over multiple time points
Time Frame: Change from Baseline, then after six weeks and after twelve weeks
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Sarubin et al., 2015; Internationally used self-report of individual resilience [short version: 10 items, each rated on a 5-point scale (0-4), with higher scores reflecting stronger resilience].
A total score will be computed with averaged item scores.
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Change from Baseline, then after six weeks and after twelve weeks
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Change on Self-assessment of Emotion Regulation Skills (Selbsteinschätzung emotionaler Kompetenzen; SEK-27) over multiple time points
Time Frame: Change from Baseline, then after six weeks and after twelve weeks
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Berking & Znoj, 2008; Self-Report Measure for the Assessment of Emotion Regulation Skills [27 items, 9 subscales, 5-point Likert scale ("not at all" to "always")].
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Change from Baseline, then after six weeks and after twelve weeks
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Change on Self-Compassion Scale (SCS-D) over multiple time points
Time Frame: Change from Baseline, then after six weeks and after twelve weeks
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Neff, 2003; Internationally used self-report of of self-compassion [26 items, 6 subscales, 5-point scale ("almost never" to "almost always")].
Participants will be asked to rate the items according to how often they behave in the stated manner towards themselves in difficult times.
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Change from Baseline, then after six weeks and after twelve weeks
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Change on Working Alliance Inventory (WAI) between two time points
Time Frame: Change from six weeks after treatment to twelve weeks after
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Wilmers et al., 2008; Internationally used self-report of therapeutic alliance measuring bond, goals and tasks in psychotherapy based on feedback of patients concerning the current therapy session [online version: 12 items, 5-point Likert scale ("rarely or never" to "always")].
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Change from six weeks after treatment to twelve weeks after
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Change on Questionnaire Assessing the Acceptance of Unpleasant and Pleasant Emotions (Fragebogen zur Akzeptanz von Gefühlen; FrAGe) over multiple time points
Time Frame: Change from Baseline, then after six weeks and after twelve weeks
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Beblo et al., 2011; Self-report of the acceptance and supression of unpleasant and unpleasant emotions [32 items, 2 subscales: Pleasant and Unpleasant emotions, 6-point scale ("strongly disagree" to "strongly agree")].
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Change from Baseline, then after six weeks and after twelve weeks
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Change on Positive and Negative Affect Schedule (PANAS) over multiple time points
Time Frame: At the beginning of every subpart of the intervention, every week up to 5 weeks
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Watson, Clark, & Tellegen, 1988; Internationally used self-report of positive and negative affect [10 items, 5-point scale ("very slightly or not at all" to "extremely")].
Participants will be asked to rate the items according to how they feel "in the current moment".
The PANAS includes two subscales of global positive affect (ten items, range: 1-5) and global negative affect (10 items, range: 1-5).
Only the subscale of global positive affect will be used.
Subscale scores are computed with averaged item scores.
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At the beginning of every subpart of the intervention, every week up to 5 weeks
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Ulrike Willutzki, Prof. Dr., Witten/Herdecke University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 221/2019
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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