Mindful Self Compassion in Rehabilitation Inpatients

January 9, 2017 updated by: Mag. Lisza Gaiswinkler, Universitätsklinik für Psychiatrie und Psychotherapeutische Medizin

Mindful Self Compassion in Rehabilitation Inpatients: a Randomized Controlled Trial

In recent years there has been convincing evidence of the positive effects of mindfulness based interventions, as a form of complementary and alternative medicine in regards to subjective well-being and physical health. There is growing evidence concerning the positive effects of these techniques in regards to an adequate stress management (e.g. respiration and heart rate variability). These findings can be found as well documented in the literature. For this study it is conducted to gain further insights into the role of mindfulness based meditation techniques for psychological well-being. Therefore it is intended to focus on clinical groups (e. g. depression and anxiety patients) in order to find out more about the relevance of mindfulness based meditation techniques as an adjunct for psychiatric and psychotherapeutic treatment. In this study special aspects of mental and spiritual health (e.g. self compassion, subjective perceived stress, spiritual well-being, and psychiatric symptoms) should be examined by comparing a group of clinical patients which practice mindfulness based meditation once a week with a control group, practicing PMR (progressive muscle relaxation)

Study Overview

Detailed Description

A holistic view of man is increasingly becoming our consciousness these days. Simultaneously, the demand for efficient and cost-effective forms of treatment for mental illness rises. According to a study by the World Health Organization (2011), 37% of "healthy" working years are lost due to psychiatric disorders. Thus complementary-alternative methods (CAM) as mindfulness-based meditation are becoming more important in medicine. A special form of mindfulness meditation-based training offers "Mindful Self Compassion (MSC)" (to German: achtsames Selbstmitgefühl). As evidence-based sister program to the well-established procedure MBSR and MBCT, MSC provides about meditation, interpersonal exercises, informal practical exercises and homework, the opportunity to learn an attentive and loving contact with itself or to improve and thus contribute effectively to comprehensive well-being. The literature reveals that MSC helps to lead a fulfilling life and is positively related to life satisfaction, emotional intelligence, happiness, optimism and personal initiative. MSC is further negatively correlated with depression, anxiety, self-criticism, the suppression of negative emotions and a negative body image. Furthermore, it is apparent from a study by Blatt (1995) that patients who are very critical towards themselves tend to have less positive effects of antidepressants, placebo and psychotherapy. For this reason it seems of enormous relevance to develop and evaluate therapies, which can help to change people's perception of oneself, like MSC. Based on these results, which show a clear link between Self-Compassion and psychological well-being, a study should be carried out which examines the effects of mindful self compassion meditation on psychological well-being and the severity of clinical symptoms and thus allows a first assessment of effectiveness in clinical practice. A randomized controlled trial is investigated at the rehabilitation center "Sonnenpark Rust Neusiedlersee" where one group of patients (at least 70 patients anticipated) will undergo a shortened form (6 weeks, 75 minutes per week) of MSC training, compared to a group of patients (at least 70 patients anticipated) who undergo regular progressive muscle relaxation (PMR). Both trainings will take place once a week for 6 weeks and will each last for 75 minutes. Patients in both groups will be asked for homework assignments and will get a handout. All relevant parameters are examined at the beginning of the rehabilitation, as well as at the end of the stay at the center. A follow- up after 6 months is planned.

Study Type

Interventional

Enrollment (Actual)

200

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

    • Steiermark
      • Graz, Steiermark, Austria, 8036
        • Universitätsklinik für Psychiatrie und Psychotherapeutische Medizin

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:

  • Written consent for study participation
  • age over 18

Exclusion Criteria:

  • psychotic episode

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Mindful Self Compassion
Participants will receive a shortened form (6 weeks) of mindful self compassion meditation, once a week for 75 minutes, furthermore they get an audio cd and a handout to practice during the week
Mindful Self Compassion (MSC) training has its primary focus on developing a friendly relationship with oneself by meditation,conversation with the group and the trainer, informal practice and homework assignments. These relationship is founded on mindfulness; therefore the participants will learn a way concentrate on the present moment. The orginal MSC training by Neff and Germer is well established, this intervention will be a shortened form of the original version and will last for the whole visit of the clinical patients in rehabilitation
Other: Progressive Muscle Relaxation
Participants will receive progressive muscle relaxation once a week for 75 minutes, furthermore they get an audio cd and a handout to practice during the week
Progressive Muscle Relaxation by Jacobson is a well known relaxation technique where participants learn to recognize the difference between tension and relaxation by tensing and subsequently relaxing the muscles. The trainingw ill last the wohole stay and the control group will also do homework assignments.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-Compassion Scale (SCS)
Time Frame: Change from Baseline values in SCS at 6 weeks, follow up 6 months after study completion
Self compassion is captured via 26 items on a 5-point rating scale. Self Compassion is measured at the beginning and at the end of the 6 weeks intervention
Change from Baseline values in SCS at 6 weeks, follow up 6 months after study completion

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Brief Symptom Inventory (BSI-18)
Time Frame: Change from Baseline values BSI-18 at 6 weeks, follow up 6 months after study completion
Anxiety, Depression and Somatization as subscales and General Symptom Burden as global score are captured via 18 items on a 4-point rating scale.
Change from Baseline values BSI-18 at 6 weeks, follow up 6 months after study completion
Health Survey (SF-36)
Time Frame: Change from Baseline values in SF-36 at 6 weeks, follow up 6 months after study completion
Health-related quality of life is captured via 36 items over different answering conditions and has 8 subscales: physical functioning, physical role ,bodily pain, general health perceptions, vitality, social functioning, emotional role function and mental well-being
Change from Baseline values in SF-36 at 6 weeks, follow up 6 months after study completion

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Sociodemographic Data/ Age
Time Frame: Baseline sociodemographic data, follow up 6 months after study completion
Digits entry
Baseline sociodemographic data, follow up 6 months after study completion
Sociodemographic Data/ Education
Time Frame: Baseline sociodemographic data, follow up 6 months after study completion
Education will be assessed by a 6-point rating scale: 1=compulsory education, 2= completed apprenticeship, 3=vocational high school, 4=high school, 5=college degree, 6= university degree and subsequently categorized (1=low education level (compulsory education, completed apprenticeship, vocational high school; 2= high education level (high school, college degree, university degree)
Baseline sociodemographic data, follow up 6 months after study completion
Sociodemographic Data/ Diet
Time Frame: Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
Dietary habits will be assessed by a 5-point rating scale (1=with meat, 2=with little meat, 3=with meat and rich in fruits and vegetables, 4=vegetarian with milk/eggs and/or fish, 5=vegan)
Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
Sociodemographic Data/ Weight and Height (BMI)
Time Frame: Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
Weight (kg) and Height (m) will be assessed by digits entry and subsequently transformed into BMI
Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
Sociodemographic Data/ Confession
Time Frame: Baseline sociodemographic data, follow up 6 months after study completion
Confession will be assessed by a 7-point rating scale (1=buddhism, 2=christianity 3=hinduism, 4=islam, 5=judaism, 6=none, 7=other)
Baseline sociodemographic data, follow up 6 months after study completion
Sociodemographic Data/ Diagnosis
Time Frame: Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
Diagnosis will be assessed by free answer and subsequently diagnosis will be categorized
Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
Sociodemographic Data/ Medication
Time Frame: Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
Medication will be assessed by free answer and subsequently diagnosis will be categorized
Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
Sociodemographic Data/ Level of Perceived Stress
Time Frame: Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
Level of Perceived Stress will be captured via 10 point rating scale (1=not at all - 10= absolutely)
Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
Sociodemographic Data/ Previous Experience with Meditation
Time Frame: Baseline sociodemographic data
dichotomous response format (0=no, 1=yes)
Baseline sociodemographic data
Sociodemographic Data/ Previous Experience with Progressive Muscle Relaxation
Time Frame: Baseline sociodemographic data
dichotomous response format (0=no, 1=yes)
Baseline sociodemographic data
Sociodemographic Data/ Previous Experience with Mindfulness
Time Frame: Baseline sociodemographic data
dichotomous response format (0=no, 1=yes)
Baseline sociodemographic data
Sociodemographic Data/ Employment
Time Frame: Baseline sociodemographic data, follow up 6 months after study completion
Employment will be assessed via 4-point rating scale (1=standing in the Profession, 2=in education, 3=retired, 4=without gainful employment)
Baseline sociodemographic data, follow up 6 months after study completion
Sociodemographic Data/ Marital Status
Time Frame: Baseline sociodemographic data, follow up 6 months after study completion
Marital Status will be assessed via 4-point rating scale (1=married, 2=partnership, 3=single, 4=widowed/divorced)
Baseline sociodemographic data, follow up 6 months after study completion
Sociodemographic Data/ Alcohol Consumption
Time Frame: Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
dichotomous response format (0=no, 1=yes)
Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
Sociodemographic Data/ Drug Consumption
Time Frame: Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
dichotomous response format (0=no, 1=yes)
Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
Sociodemographic Data/ Nicotine Consumption
Time Frame: Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
dichotomous response format (0=no, 1=yes), if answered with "yes" it is asked for the amount of cigarettes consumed per day
Changes from Baseline sociodemographic data at 6 weeks, follow up 6 months after study completion
Sociodemographic Data/ Sympathy of the learned practice (either MSC or PMR)
Time Frame: sociodemographic data at 6 weeks, follow up 6 months after study completion
will be captured via 10 point rating scale (1=not at all - 10= absolutely)
sociodemographic data at 6 weeks, follow up 6 months after study completion
Sociodemographic Data/ Sympathy of the trainer (either MSC or PMR)
Time Frame: sociodemographic data at 6 weeks, follow up 6 months after study completion
will be captured via 10 point rating scale (1=not at all - 10= absolutely)
sociodemographic data at 6 weeks, follow up 6 months after study completion
Sociodemographic Data/ Duration of Practice
Time Frame: sociodemographic data at 6 weeks, follow up 6 months after study completion
dichotomous response format (0=no, 1=yes), if answered with "yes" (I practice MSC/PMR) it is asked for the amount of practice per day with a 3-point rating scale (1=less than 10 minutes, 2= 10-15 minutes, 3=more than 15 minutes)
sociodemographic data at 6 weeks, follow up 6 months after study completion
Sociodemographic Data/ Frequency of Practice
Time Frame: sociodemographic data at 6 weeks, follow up 6 months after study completion
dichotomous response format (0=no, 1=yes), if answered with "yes" (I practice MSC/PMR) it is asked for the frequency of practice per day with a 4-point rating scale (1=daily, 2=serveral times a week, 3=once per week, 4=less than once a week)
sociodemographic data at 6 weeks, follow up 6 months after study completion
Sociodemographic Data/ Type of Practice
Time Frame: sociodemographic data at 6 weeks, follow up 6 months after study completion
dichotomous response format (0=no, 1=yes), if answered with "yes" (I practice MSC/PMR) it is asked for the type (ritualized vs. informal) of practice
sociodemographic data at 6 weeks, follow up 6 months after study completion
Subjective Feeling of Health
Time Frame: Changes from Baseline data at 6 weeks, follow up 6 months after study completion
will be captured via 10 point rating scale (1=not at all - 10= absolutely)
Changes from Baseline data at 6 weeks, follow up 6 months after study completion
Subjective Feeling of Happines
Time Frame: Changes from Baseline data at 6 weeks, follow up 6 months after study completion
will be captured via 10 point rating scale (1=not at all - 10= absolutely)
Changes from Baseline data at 6 weeks, follow up 6 months after study completion
Previous Experience with Yoga
Time Frame: Baseline sociodemographic data, captured at the beginning
dichotomous response format (0=no, 1=yes)
Baseline sociodemographic data, captured at the beginning
Previous Experience with Mindful Self Compassion
Time Frame: Baseline sociodemographic data, captured at the beginning
dichotomous response format (0=no, 1=yes)
Baseline sociodemographic data, captured at the beginning

Collaborators and Investigators

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

Collaborators

Investigators

  • Principal Investigator: Human-Friedrich Unterrainer, Priv.Doz., Universitätsklinik für Psychiatrie/Medizinische Univeristät Graz

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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

December 1, 2015

Primary Completion (Actual)

November 1, 2016

Study Completion (Actual)

November 1, 2016

Study Registration Dates

First Submitted

October 9, 2015

First Submitted That Met QC Criteria

October 14, 2015

First Posted (Estimate)

October 19, 2015

Study Record Updates

Last Update Posted (Estimate)

January 10, 2017

Last Update Submitted That Met QC Criteria

January 9, 2017

Last Verified

January 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • ECS 1392/2015

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

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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