- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04917081
'Go With the Flow': Effects of Mindful Self-Compassion in Psychiatric Rehabilitation
This study is designed as a randomized controlled trial to gain further insights into possible effects of a standardized 6-week Mindful Self-Compassion (MSC) training on psychiatric rehabilitation inpatients and aims
- to generate insights into which parameters of mental health, and especially emotion regulation, can be improved by MSC in this setting,
- to compare effects of MSC training with an established relaxation training (i.e., progressive muscle relaxation; PMR) and
- to determine the general conditions and patient characteristics influencing the effectiveness of MSC training.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
Burgenland
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Rust, Burgenland, Austria, 7071
- pro mente REHA, Sonnenpark Neusiedlersee
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Psychiatric diagnosis
- Signed informed consent form
- Full command of the German language
Exclusion Criteria:
- Age <18 years
- Acute psychotic episode, acute suicidal tendencies, and acute addiction disorders
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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EXPERIMENTAL: Mindful Self-Compassion
|
Mindful Self-Compassion has been developed by Neff and Germer as a specific kind of Mindfulness-Based Interventions to promote self-compassion.
It combines the skills of mindfulness and self-compassion, providing a powerful tool for emotional resilience and enhancing the capacity for emotional wellbeing.
In this study, a shortened version of the MSC program is used which is applied once a week for 75 minutes throughout the patients' stay in the rehabilitation clinic.
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ACTIVE_COMPARATOR: Progressive Muscle Relaxation
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Progressive Muscle Relaxation by Jacobson is a deep relaxation technique that helps relieve muscle tension and is based on the premise that mental calmness is a natural result of physical relaxation.
In this study, Progressive Muscle Relaxation is applied once a week for 75 minutes throughout the patients' stay in the rehabilitation clinic.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Emotion Regulation Questionnaire (ERQ)
Time Frame: Baseline and 1 day after the last intervention
|
The Emotion Regulation Questionnaire (ERQ) measures two common emotion regulation strategies (cognitive reappraisal and expressive suppression) with a total of 10 items (reappraisal scale: 6 items; suppression scale: 4 items), which are answered on a seven-point Likert scale ranging from 1 (strongly disagree) to 7 (strongly agree).
The higher the score of a scale (mean value ranging from 1 to 7), the more frequently the respective emotion regulation strategy is used.
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Baseline and 1 day after the last intervention
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Change in Positive and Negative Affect Schedule (PANAS)
Time Frame: Baseline and 1 day after the last intervention
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The Positive and Negative Affect Schedule (PANAS) consists of 20 items and captures two dispositional dimensions (positive affect and negative affect), 10 items for each scale.
A five-point Likert scale (1 - very slightly to 5 - extremely) is used.
Mean scores for each of the two scales can range from 1 to 5, with lower scores representing lower levels of positive/negative affect and higher scores representing higher levels of positive/negative affect.
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Baseline and 1 day after the last intervention
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Reappraisal Inventiveness Test (RIT)
Time Frame: 1 day after the last intervention
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The Reappraisal Inventiveness Test (RIT) assesses emotion regulation abilities on a behavioral level.
Participants generate cognitive reappraisals for different anger-provoking situations to reduce their anger.
The fluency (total number of generated nonidentical ideas that qualified as cognitive reappraisals) and flexibility (number of categorically different reappraisals) of these reappraisals are measured.
The given answers will be independently rated by two researchers.
In addition, the intensity of induced anger will be assessed with a seven-point Likert scale from 0 (not at all) to 6 (very).
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1 day after the last intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Self-Compassion Scale (SCS)
Time Frame: Baseline and 1 day after the last intervention
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SCS captures the amount of self-compassion by means of 26 items answered on a five-point Likert scale (1 to 5).
A higher value (mean value ranging from 1 to 5) indicates a higher level of self-compassion.
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Baseline and 1 day after the last intervention
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Change in Short-Form-Health Survey (SF-12)
Time Frame: Baseline and 1 day after the last intervention
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SF-12 measures quality of life via 12 items answered with different response formats.
The items are weighted and summed to provide a physical and mental health score ranging from 0 to 100, with a higher score indicating better health.
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Baseline and 1 day after the last intervention
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Change in Brief Symptom Inventory (BSI-18)
Time Frame: Baseline and 1 day after the last intervention
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The BSI-18 assesses psychiatric symptoms in three dimensions (somatization, depression and anxiety), which can be summarized in a global severity index (GSI).
It contains 18 items that are answered on a five-point Likert scale ranging from 0 (not at all) to 4 (extremely).
Higher values (ranging from 0 to 24 in the three dimensions; ranging from 0 to 72 in the GSI) indicate a greater severity of symptoms.
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Baseline and 1 day after the last intervention
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Change in Multidimensional Inventory for Religious/Spiritual Well-Being 12 (MI-RSB 12)
Time Frame: Baseline and 1 day after the last intervention
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The MI-RSB 12 captures four different dimensions of religious and spiritual well-being, namely general religiosity, forgiveness, connectedness, and immanent hope, which can be collated into a total amount of religious/spiritual well-being (RSB).
The instrument consists of 12 items, three items per dimension, answered via a six-point Likert scale (1 - strongly disagree to 6 - strongly agree).
Scores range from 3 to 18 for each subscale and from 12 to 72 for the overall score of the RSB.
Higher scores indicate higher religious and spiritual well-being.
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Baseline and 1 day after the last intervention
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Change in Happiness
Time Frame: every day during the stay at the rehabilitation clinic
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The amount of subjective happiness will be captured by one item, which has to be answered on a 10-point Likert scale, with 1 indicating "not happy at all" and 10 "absolutely happy".
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every day during the stay at the rehabilitation clinic
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Inventory of Personality Organization (IPO-16)
Time Frame: Baseline and 1 day after the last intervention
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Personality structure will be assessed with the IPO-16 which consists of the three subscales identity diffusion, primitive defenses, and reality testing.
The 16 items (identity diffusion: 6 items; primitive defenses: 5 items; reality testing: 5 items) are rated on a five-point Likert scale ranging from 1 (never) to 5 (always).
A global index is used for statistical analysis, which is gathered by the mean of all items and ranges between 1 and 5.
A higher value indicates a higher structural impairment.
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Baseline and 1 day after the last intervention
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Experience in Close Relationships (Revised, German Version; ECR-RD12)
Time Frame: Baseline and 1 day after the last intervention
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To assess general attachment patterns, the ECR-RD12 will be used.
This questionnaire assesses attachment-related anxiety (6 items) and attachment-related avoidance (6 items) with a total of 12 items, rated on a seven-point Likert scale from 1 (strongly disagree) to 7 (strongly agree).
Scale-scores range between 1 and 7. Higher scores on one or both dimensions are considered to indicate an insecure adult attachment orientation.
Lower scores indicate a secure adult attachment orientation.
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Baseline and 1 day after the last intervention
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Sex
Time Frame: Baseline and 1 day after the last intervention
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Two questions are used to assess sex at birth and current sex with the following response options: 1 - female, 2 - male, 3 - transgender, 4 - other.
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Baseline and 1 day after the last intervention
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Age
Time Frame: Baseline
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Digit entry
|
Baseline
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Weight and Height (BMI)
Time Frame: Baseline and 1 day after the last intervention
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Weight (kg) and height (cm) will be assessed by digits entry and subsequently transformed into BMI.
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Baseline and 1 day after the last intervention
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Education
Time Frame: Baseline
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Education will be assessed via six response options (1 - compulsory education, 2 - completed apprenticeship, 3 - vocational high school, 4 - high school, 5 - college degree, 6 - university degree).
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Baseline
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Employment
Time Frame: Baseline
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Employment will be assessed via four response options (1 - standing in the profession, 2 - in education, 3 - retired, 4 - without gainful employment).
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Baseline
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Marital status
Time Frame: Baseline
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Marital status will be assessed via four response options (1 - married, 2 - partnership, 3 - single, 4 - widowed/divorced).
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Baseline
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Confession
Time Frame: Baseline
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Confession will be assessed via six response options (1 - Christianity, 2 - Buddhism, 3 - Hinduism, 4 - Islam, 5 - none, 6 - other).
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Baseline
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Children
Time Frame: Baseline
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Participants are asked whether they have children using a dichotomous response format (0 - no, 1- yes).
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Baseline
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Diet
Time Frame: Baseline and 1 day after the last intervention
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Dietary habits will be assessed with the following response options: 1 - with a lot of meat, 2 - with little meat, 3 - with meat and rich in fruits and vegetables, 4 - vegetarian with fish and/or milk/eggs, 5 - vegan. In addition, it is also asked whether this diet has been followed for at least 6 months (0 - no, 1 - yes). |
Baseline and 1 day after the last intervention
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Cigarettes per day
Time Frame: Baseline and 1 day after the last intervention
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Digit entry
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Baseline and 1 day after the last intervention
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Alcohol consumption
Time Frame: Baseline and 1 day after the last intervention
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dichotomous response format (0 - no, 1 - yes)
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Baseline and 1 day after the last intervention
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Consumption of illegal drugs
Time Frame: Baseline and 1 day after the last intervention
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dichotomous response format (0 - no, 1 - yes)
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Baseline and 1 day after the last intervention
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Medication
Time Frame: Baseline and 1 day after the last intervention
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Medication will be assessed by free answer.
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Baseline and 1 day after the last intervention
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Mental illness
Time Frame: Baseline and 1 day after the last intervention
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Mental illness will be assessed by free answer.
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Baseline and 1 day after the last intervention
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Subjective feeling of health
Time Frame: Baseline and 1 day after the last intervention
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Subjective feeling of health will be captured via a ten-point rating scale (1 - not at all to 10 - absolutely).
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Baseline and 1 day after the last intervention
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Religiosity
Time Frame: Baseline and 1 day after the last intervention
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Religiosity will be captured via a ten-point rating scale (1 - not at all to 10 - absolutely).
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Baseline and 1 day after the last intervention
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Spirituality
Time Frame: Baseline and 1 day after the last intervention
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Spirituality will be captured via a ten-point rating scale (1 - not at all to 10 - absolutely).
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Baseline and 1 day after the last intervention
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Previous experience with meditation
Time Frame: Baseline
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dichotomous response format (0 - no, 1 - yes)
|
Baseline
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Previous experience with yoga
Time Frame: Baseline
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dichotomous response format (0 - no, 1 - yes)
|
Baseline
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Previous experience with mindfulness
Time Frame: Baseline
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dichotomous response format (0 - no, 1 - yes)
|
Baseline
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Previous experience with Progressive Muscle Relaxation (PMR)
Time Frame: Baseline
|
dichotomous response format (0 - no, 1 - yes)
|
Baseline
|
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Previous experience with Mindful Self-Compassion (MSC)
Time Frame: Baseline
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dichotomous response format (0 - no, 1 - yes)
|
Baseline
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Practice of the learned practice (either PMR or MSC)
Time Frame: 1 day after the last intervention
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dichotomous response format (0 - no, 1 - yes); if answered with "yes" (I practice PMR/MSC) it is asked for the frequency of practice (1 - daily, 2 - several times a week, 3 - once a week, 4 - less than once a week), the duration of practice (1 - less than 10 minutes, 2 - 10-15 minutes, 3 - more than 15 minutes), and the type of practice (1 - ritualized, 2 - informal)
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1 day after the last intervention
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Sympathy of the learned practice (either PMR or MSC)
Time Frame: 1 day after the last intervention
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Subjective sympathy of the learned practice will be captured via a ten-point rating scale (1 - not at all to 10 - absolutely).
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1 day after the last intervention
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Sympathy of the trainer (either PMR or MSC)
Time Frame: 1 day after the last intervention
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Subjective sympathy of the trainer will be captured via a ten-point rating scale (1 - not at all to 10 - absolutely).
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1 day after the last intervention
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Human-Friedrich Unterrainer, PD DDr., Medical University Graz, Department of Psychiatry and Psychotherapeutic Medicine
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
Keywords
Other Study ID Numbers
- MUGrazXXX
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
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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