Emotional Competence and Compassion Online-Training (ECCO)
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03789929 |
|
Recruitment Status : Unknown
Verified February 2019 by Andreas Michalsen, Charite University, Berlin, Germany.
Recruitment status was: Recruiting
First Posted : December 31, 2018
Last Update Posted : February 12, 2019
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
| Condition or disease | Intervention/treatment |
|---|---|
| Emotional Intelligence | Behavioral: The Emotional Backpack Behavioral: Feelings as Powers |
Stress and stress related diseases are becoming a huge health burden in modern societies. Psycho-emotional stress plays a key role in stress regulation. Therefore this study aims to investigate the effects of online-courses addressing emotion regulation.
For this aim several different online-courses about emotional competence and compassion are scientifically evaluated with psychometric questionnaires and heart rate variability measuring. The courses are planned by the trainers and people register on their own initiative.
The courses have a duration of 4 weeks or three months. They consist of video lectures that explain the content as well as videos giving exercises about the character of the different feelings and about the characteristics of emotions. They teach practices on how to use feelings as an empowering force in life and how to deal with difficult emotions.
| Study Type : | Observational |
| Estimated Enrollment : | 400 participants |
| Observational Model: | Cohort |
| Time Perspective: | Prospective |
| Official Title: | Scientific Evaluation of Online-Trainings for Emotional Competence, Compassion and Relationship Competences |
| Actual Study Start Date : | January 1, 2019 |
| Estimated Primary Completion Date : | December 31, 2019 |
| Estimated Study Completion Date : | July 31, 2020 |
| Group/Cohort | Intervention/treatment |
|---|---|
|
The Emotional Backpack
Healthy adults participating in the offered online-course on their own initiative.
|
Behavioral: The Emotional Backpack
In this 4 weeks course participants learn how to process difficult emotions that has been overwhelming in the past. They learn how they can use the support of other people and support other people in the processing emotions within a simple and easy to learn setting. |
|
Feelings as Powers
Healthy adults participating in the offered online-course on their own initiative.
|
Behavioral: Feelings as Powers
In this 3 months course participants learn about the empowering potential of their feelings as well as the difficult aspects of them. In addition to that they learn techniques how to deal with difficult emotions. |
- Self-Report Measure for the Assessment of Emotion Regulation Skills (SEK-27) [ Time Frame: Assessing change from baseline to 3 months and 6 months after baseline in single workshops and baseline to 3, 6, 9 and 12 months after baseline in the yearly program ]Assessing full scale, range 0-108, higher score meaning a better outcome
- Saarbrücken Personality Questionnaire (SPF) based on the Interpersonal Reactivity Index (IRI) [ Time Frame: Assessing change from baseline to 3 months and 6 months after baseline in single workshops and baseline to 3, 6, 9 and 12 months after baseline in the yearly program ]Assessing full scale, range 16-80, higher score meaning a better outcome
- The World Health Organisation- Five Well-Being Index (WHO-5) [ Time Frame: Assessing change from baseline to 3 months and 6 months after baseline in single workshops and baseline to 3, 6, 9 and 12 months after baseline in the yearly program ]Assessing full scale, range 0-100, higher score meaning a better outcome
- General Self-efficacy Short Scale (ASKU) [ Time Frame: Assessing change from baseline to 3 months and 6 months after baseline in single workshops and baseline to 3, 6, 9 and 12 months after baseline in the yearly program ]Assessing full scale, range 3-15, higher score meaning a better outcome
- Hospital Anxiety and Depression Scale (HADS) [ Time Frame: Assessing change from baseline to 3 months and 6 months after baseline in single workshops and baseline to 3, 6, 9 and 12 months after baseline in the yearly program ]Assessing full scale, range 0-42, lower score meaning a better outcome
- Mindful Attention Awareness Scale (MAAS) [ Time Frame: Assessing change from baseline to 3 months and 6 months after baseline in single workshops and baseline to 3, 6, 9 and 12 months after baseline in the yearly program ]Assessing full scale, range 15-90, higher score meaning a better outcome
- Perceived Stress Scale (PSS-10) [ Time Frame: Assessing change from baseline to 3 months and 6 months after baseline in single workshops and baseline to 3, 6, 9 and 12 months after baseline in the yearly program ]Assessing full scale, range 0-40, lower score meaning a better outcome
- Medical Outcomes Study Short Form (MOS SF-36) [ Time Frame: Assessing change from baseline to 3 months and 6 months after baseline in single workshops and baseline to 3, 6, 9 and 12 months after baseline in the yearly program ]Assessing full scale, range 0-100, higher score meaning a better outcome
- Heart Rate Variability (HRV) [ Time Frame: Assessing change from baseline to 3 and 6 months after baseline in the yearly program ]24h measuring
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years to 85 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- 18-85 years
- participation in one of the included courses
- e-mail address
Exclusion Criteria:
- participation in another study
- no verbal communication (german) possible
- dementia or another disease that limits cognitive abilities
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03789929
| Contact: Michael Jeitler, Dr. | +49 30 80505 693 | michael.jeitler@charite.de | |
| Contact: Vanessa Bähr | +49 176 32360472 | vanessa.baehr@charite.de |
| Germany | |
| Charité Medical University, Department of Integrative Medicine at the Immanual Hospital Berlin | Recruiting |
| Berlin-Zehlendorf, Berlin, Germany, 14109 | |
| Contact: Miriam Roesner 030 - 80505 - 682 m.roesner@immanuel.de | |
| Principal Investigator: | Andreas Michalsen, prof. Dr. | Charite - Universitätsmedizin Berlin |
| Responsible Party: | Andreas Michalsen, Principal Investigator, Charite University, Berlin, Germany |
| ClinicalTrials.gov Identifier: | NCT03789929 |
| Other Study ID Numbers: |
ECCO |
| First Posted: | December 31, 2018 Key Record Dates |
| Last Update Posted: | February 12, 2019 |
| Last Verified: | February 2019 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
|
Stress Emotion |

