'Go With the Flow': Effects of Mindful Self-Compassion in Psychiatric Rehabilitation

April 5, 2022 updated by: Medical University of Graz

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

Study Type

Interventional

Enrollment (Actual)

233

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

    • Burgenland
      • Rust, Burgenland, Austria, 7071
        • pro mente REHA, Sonnenpark Neusiedlersee

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

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Psychiatric diagnosis
  2. Signed informed consent form
  3. Full command of the German language

Exclusion Criteria:

  1. Age <18 years
  2. Acute psychotic episode, acute suicidal tendencies, and acute addiction disorders

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
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
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.
ACTIVE_COMPARATOR: Progressive Muscle Relaxation
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.

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.
Baseline and 1 day after the last intervention
Change in Positive and Negative Affect Schedule (PANAS)
Time Frame: Baseline and 1 day after the last intervention
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.
Baseline and 1 day after the last intervention
Reappraisal Inventiveness Test (RIT)
Time Frame: 1 day after the last intervention
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).
1 day after the last intervention

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
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.
Baseline and 1 day after the last intervention
Change in Short-Form-Health Survey (SF-12)
Time Frame: Baseline and 1 day after the last intervention
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.
Baseline and 1 day after the last intervention
Change in Brief Symptom Inventory (BSI-18)
Time Frame: Baseline and 1 day after the last intervention
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.
Baseline and 1 day after the last intervention
Change in Multidimensional Inventory for Religious/Spiritual Well-Being 12 (MI-RSB 12)
Time Frame: Baseline and 1 day after the last intervention
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.
Baseline and 1 day after the last intervention
Change in Happiness
Time Frame: every day during the stay at the rehabilitation clinic
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".
every day during the stay at the rehabilitation clinic

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
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.
Baseline and 1 day after the last intervention
Experience in Close Relationships (Revised, German Version; ECR-RD12)
Time Frame: Baseline and 1 day after the last intervention
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.
Baseline and 1 day after the last intervention
Sex
Time Frame: Baseline and 1 day after the last intervention
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.
Baseline and 1 day after the last intervention
Age
Time Frame: Baseline
Digit entry
Baseline
Weight and Height (BMI)
Time Frame: Baseline and 1 day after the last intervention
Weight (kg) and height (cm) will be assessed by digits entry and subsequently transformed into BMI.
Baseline and 1 day after the last intervention
Education
Time Frame: Baseline
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).
Baseline
Employment
Time Frame: Baseline
Employment will be assessed via four response options (1 - standing in the profession, 2 - in education, 3 - retired, 4 - without gainful employment).
Baseline
Marital status
Time Frame: Baseline
Marital status will be assessed via four response options (1 - married, 2 - partnership, 3 - single, 4 - widowed/divorced).
Baseline
Confession
Time Frame: Baseline
Confession will be assessed via six response options (1 - Christianity, 2 - Buddhism, 3 - Hinduism, 4 - Islam, 5 - none, 6 - other).
Baseline
Children
Time Frame: Baseline
Participants are asked whether they have children using a dichotomous response format (0 - no, 1- yes).
Baseline
Diet
Time Frame: Baseline and 1 day after the last intervention

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
Cigarettes per day
Time Frame: Baseline and 1 day after the last intervention
Digit entry
Baseline and 1 day after the last intervention
Alcohol consumption
Time Frame: Baseline and 1 day after the last intervention
dichotomous response format (0 - no, 1 - yes)
Baseline and 1 day after the last intervention
Consumption of illegal drugs
Time Frame: Baseline and 1 day after the last intervention
dichotomous response format (0 - no, 1 - yes)
Baseline and 1 day after the last intervention
Medication
Time Frame: Baseline and 1 day after the last intervention
Medication will be assessed by free answer.
Baseline and 1 day after the last intervention
Mental illness
Time Frame: Baseline and 1 day after the last intervention
Mental illness will be assessed by free answer.
Baseline and 1 day after the last intervention
Subjective feeling of health
Time Frame: Baseline and 1 day after the last intervention
Subjective feeling of health will be captured via a ten-point rating scale (1 - not at all to 10 - absolutely).
Baseline and 1 day after the last intervention
Religiosity
Time Frame: Baseline and 1 day after the last intervention
Religiosity will be captured via a ten-point rating scale (1 - not at all to 10 - absolutely).
Baseline and 1 day after the last intervention
Spirituality
Time Frame: Baseline and 1 day after the last intervention
Spirituality will be captured via a ten-point rating scale (1 - not at all to 10 - absolutely).
Baseline and 1 day after the last intervention
Previous experience with meditation
Time Frame: Baseline
dichotomous response format (0 - no, 1 - yes)
Baseline
Previous experience with yoga
Time Frame: Baseline
dichotomous response format (0 - no, 1 - yes)
Baseline
Previous experience with mindfulness
Time Frame: Baseline
dichotomous response format (0 - no, 1 - yes)
Baseline
Previous experience with Progressive Muscle Relaxation (PMR)
Time Frame: Baseline
dichotomous response format (0 - no, 1 - yes)
Baseline
Previous experience with Mindful Self-Compassion (MSC)
Time Frame: Baseline
dichotomous response format (0 - no, 1 - yes)
Baseline
Practice of the learned practice (either PMR or MSC)
Time Frame: 1 day after the last intervention
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)
1 day after the last intervention
Sympathy of the learned practice (either PMR or MSC)
Time Frame: 1 day after the last intervention
Subjective sympathy of the learned practice will be captured via a ten-point rating scale (1 - not at all to 10 - absolutely).
1 day after the last intervention
Sympathy of the trainer (either PMR or MSC)
Time Frame: 1 day after the last intervention
Subjective sympathy of the trainer will be captured via a ten-point rating scale (1 - not at all to 10 - absolutely).
1 day after the last intervention

Collaborators and Investigators

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

Collaborators

Investigators

  • Principal Investigator: Human-Friedrich Unterrainer, PD DDr., Medical University Graz, Department of Psychiatry and Psychotherapeutic Medicine

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)

September 11, 2020

Primary Completion (ACTUAL)

August 11, 2021

Study Completion (ACTUAL)

August 11, 2021

Study Registration Dates

First Submitted

May 27, 2021

First Submitted That Met QC Criteria

June 7, 2021

First Posted (ACTUAL)

June 8, 2021

Study Record Updates

Last Update Posted (ACTUAL)

April 6, 2022

Last Update Submitted That Met QC Criteria

April 5, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • MUGrazXXX

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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.

Clinical Trials on Progressive Muscle Relaxation

Clinical Trials on Mindful Self-Compassion

Subscribe