- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02578433
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
Status
Completed
Conditions
Intervention / Treatment
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
-
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Steiermark
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Graz, Steiermark, Austria, 8036
- Universitätsklinik für Psychiatrie und Psychotherapeutische Medizin
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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)
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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
- Balasubramaniam M, Telles S, Doraiswamy PM. Yoga on our minds: a systematic review of yoga for neuropsychiatric disorders. Front Psychiatry. 2013 Jan 25;3:117. doi: 10.3389/fpsyt.2012.00117. eCollection 2012.
- Barnett JE, Shale AJ. The Integration of Complementary and Alternative Medicine (CAM) into the Practice of Psychology: A Vision for the Future. Professional Psychology. Resarch and Practice 43: 576-585, 2012.
- Foryflow AL. Integrating Yoga with Psychotherapy: A Complementary Treatment for Anxiety and Depression. Canadian Journal of Counselling and Psychotherapy 45: 132-150, 2011.
- World Health Organization. Global Status Report on Non-Communicable Diseases. Geneva:WHO 2010, 2011.
- Blatt SJ. Representational structures in psychopathology. University of Rochester Press 6: 1-34, 1995
- Bullinger M. German translation and psychometric testing of the SF-36 Health Survey: preliminary results from the IQOLA Project. International Quality of Life Assessment. Soc Sci Med. 1995 Nov;41(10):1359-66. doi: 10.1016/0277-9536(95)00115-n.
- Spitzer C, Hammer S, Lowe B, Grabe HJ, Barnow S, Rose M, Wingenfeld K, Freyberger HJ, Franke GH. [The short version of the Brief Symptom Inventory (BSI -18): preliminary psychometric properties of the German translation]. Fortschr Neurol Psychiatr. 2011 Sep;79(9):517-23. doi: 10.1055/s-0031-1281602. Epub 2011 Aug 25. German.
- Neff KD. Development and validation of a scale to measure self-compassion. Self and Identity 2: 223-250, 1993.
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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