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

The study's aim is to determine whether brief interventions (micro-interventions) aiming to optimize expectations or enhancing feelings of self-compassion are able to improve well-being/reduce perceived stress in comparison to an active control group in an online-study

Study Overview

Detailed Description

In this study we use a pre-post-test design to compare the effects of the (classic) best possible self intervention vs. the best possible self intervention (including ways on how to reach the imagined best possible future) vs. a self-compassion intervention vs. an active control group. We are interested in the differential effects and examine several moderators.

Study Type

Interventional

Enrollment (Actual)

181

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Hessen
      • Marburg, Hessen, Germany, 35032
        • Philipps University Marburg

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 6, 2020

Primary Completion (Actual)

October 19, 2020

Study Completion (Actual)

October 19, 2020

Study Registration Dates

First Submitted

June 23, 2020

First Submitted That Met QC Criteria

July 1, 2020

First Posted (Actual)

July 8, 2020

Study Record Updates

Last Update Posted (Actual)

August 7, 2024

Last Update Submitted That Met QC Criteria

August 6, 2024

Last Verified

August 1, 2024

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)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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