- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04461548
Micro-interventions Aiming to Optimize Expectations or Self-compassion to Improve Well-being/Reduce Stress and Their Differential Effects
Micro-interventions Aiming to Optimize Expectations or Self-compassiong and Their Differential Effects
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Hessen
-
Marburg, Hessen, Germany, 35032
- Philipps University Marburg
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- fluent in German language
- access to a computer/tablet/smartphone with audio output/headphones
Exclusion Criteria:
- not willing to take part in an online-intervention (duration: 60 minutes)
- no access to a computer/tablet/smartphone with audio output/headphones
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group 1: Best Possible Self
Participants are asked to think and write about their best possible future self and to imagine this positive future subsequently.
|
All participants are asked to take some time to think and write about the content of the respective intervention group.
After the writing exercise (approx.
15-20 min) participants are asked to imagine that content for about 5 minutes.
|
|
Experimental: Experimental group 2: Best Possible Self + next steps
Participants are asked to think and write about their best possible future self and what the next steps could be to reach that best possible future.
Subsequently, participants are asked to imagine this positive future.
|
All participants are asked to take some time to think and write about the content of the respective intervention group.
After the writing exercise (approx.
15-20 min) participants are asked to imagine that content for about 5 minutes.
|
|
Experimental: Experimental group 3: Self-compassion
Participants are asked to think and write about a self-compassion exercise and to imagine this content subsequently.
|
All participants are asked to take some time to think and write about the content of the respective intervention group.
After the writing exercise (approx.
15-20 min) participants are asked to imagine that content for about 5 minutes.
|
|
Active Comparator: Active control group
Participants are asked to think and write about a neutral task that is comparable to the experimental groups.
|
All participants are asked to take some time to think and write about the content of the respective intervention group.
After the writing exercise (approx.
15-20 min) participants are asked to imagine that content for about 5 minutes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in perceived stress ratings
Time Frame: Change from pre (baseline) to post scores (approx. 30 minutes later)
|
Participants are asked to rate how stressed they feel at the moment at two time points (baseline and the intervention) on a questionnaire (VAS: item ranges from 0 (not stressed at all) - 100 (very stressed). Change scores are calculated (post- minus pre-scores; pre-scores will be used as a covariate). e.g.Lesage, F.-X., Berjot, S., & Deschamps, F. (2012). Clinical stress assessment using a visual ana-logue scale. Occupational Medicine, 62(8), 600-605. https://doi.org/10.1093/occmed/kqs140 |
Change from pre (baseline) to post scores (approx. 30 minutes later)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in perceived (stress) burden ratings (resulting from perceived stress)
Time Frame: Change from pre (baseline) to post scores (approx. 30 minutes later)
|
Participants are asked to rate how burdened they feel at the moment at two time points (baseline and the intervention) due to the experienced stress on a questionnaire (VAS: item ranges from 0 (not at all) - 100 (very much).
Change scores are calculated (post- minus pre-scores; pre-scores will be used as a covariate).
Indirect/opposite measure of well-being.
|
Change from pre (baseline) to post scores (approx. 30 minutes later)
|
|
Change in emotions (PANAS)
Time Frame: Change from pre (baseline) to post scores (approx. 30 minutes later)
|
Change scores are calculated for positive and negative sum scores (post- minus pre-scores; pre-scores will be used as a covariate). Krohne, H.W., Egloff, B., Kohlmann, C.W., & Tausch, A. (1996). Experiments with a German version of the "Positive and Negative Affect Schedule (PANAS). Diagnostica, 42, 139-156. |
Change from pre (baseline) to post scores (approx. 30 minutes later)
|
|
Change in state optimism ratings
Time Frame: Change from pre (baseline) to post scores (approx. 30 minutes later)
|
State Optimism measure (SOM), 7 items (each item 1(strongly disagree)-5(strongly agree)).
Change scores are calculated for positive and negative sum scores (post- minus pre-scores; pre-scores will be used as a covariate).
Millstein, R. A., Chung, W. J., Hoeppner, B. B., Boehm, J. K., Legler, S. R., Mastromauro, C. A., & Huffman, J. C. (2019).
Development of the State Optimism Measure.
General hospital psychiatry, 58, 83-93
|
Change from pre (baseline) to post scores (approx. 30 minutes later)
|
|
Change in state self-compassion
Time Frame: Change from pre (baseline) to post scores (approx. 30 minutes later)
|
Change in state self-compassion (SCS-state), 16 items (each item 1(strongly disagree) - 5 (strongly agree)). Change scores are calculated (post- minus pre-scores; pre-scores will be used as a covariate). Breines, J. G., & Chen, S. (2013). Activating the inner caregiver: The role of support-giving schemas in increasing state self-compassion. Journal of Experimental Social Psychology, 49(1), 58-64. https://doi.org/10.1016/j.jesp.2012.07.015 |
Change from pre (baseline) to post scores (approx. 30 minutes later)
|
|
Satisfaction ratings with the respective intervention
Time Frame: Only Post-Assessment (end of the experiment; approx. 45-60 minutes after start of the experiment)
|
e.g.
"I was satisfied with the intervention" or "I feel like I had a benefit from this intervention"
|
Only Post-Assessment (end of the experiment; approx. 45-60 minutes after start of the experiment)
|
|
Ratings directly assessing the perceived change due to the intervention
Time Frame: Only Post-Assessment (end of the experiment; approx. 45-60 minutes after start of the experiment)
|
e.g.
"The intervention reduced my perceived stress", "The intervention increased my feeling of being able to influence things"
|
Only Post-Assessment (end of the experiment; approx. 45-60 minutes after start of the experiment)
|
|
Change in perceived self-efficacy (expectations)
Time Frame: Change from pre (baseline) to post scores (approx. 30 minutes later)
|
Change in perceived self-efficacy (SWE), 10 items (each item (1(not at all) - 4(exactly)). Change scores are calculated (post- minus pre-scores; pre-scores will be used as a covariate). SchwarzerR& Jerusalem M. Generalized Self---Efficacy scale. In J. Weinman, S. Wright, &M. Johnston, Measures in health psychology: A user's portfolio. Causal andcontrol beliefs (pp. 35---37). 1995. Windsor, England: NFER---NELSON. |
Change from pre (baseline) to post scores (approx. 30 minutes later)
|
|
Change in anxiety and depression state (STADI)
Time Frame: Change from pre (baseline) to post scores (approx. 30 minutes later)
|
Change in anxiety and depression state (STADI), 20 items (each item 1(strongly disagree) - 4 (strongly agree)). Change scores are calculated (post- minus pre-scores; pre-scores will be used as a covariate). Laux, L., Hock, M., Bergner-Köther, R., Hodapp, V., & Renner, K. H. (2013). The State-Trait-Anxiety-Depression-Inventory-Manual. Göttingen, Germany: Hogrefe. |
Change from pre (baseline) to post scores (approx. 30 minutes later)
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Other Study ID Numbers
- Micro_expect_compass
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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