- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03233958
The Psychosocial Effects of Systemic / Family Constellation
The Psychosocial Effects of Systemic / Family Constellation: An Observational Follow-up Study
The purpose of this study is to investigate the psychosocial effects of systemic / family constellation. The method of systemic / family constellation refers to an approach which integrates ideas from family systems therapy with elements from psychodrama. The constellations are conducted in a group based seminar-setting, each seminar lasting two days.
Considering the very limited amount of empirical data on this method, the study design is a simple pre-post one with a 6-months follow-up. The study will be observational: the researchers will not manipulate who receives the intervention; instead they invite all clients (individuals from the general population) attending these therapeutic workshops run independently of the research process. Given the limited amount of evidence on this therapeutic method, special attention will be given to monitor potential adverse outcomes to establish intervention safety.
It is hypothesized that participation in a family constellation seminar might decrease potential psychological symptoms and will not result in adverse outcomes.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Budapest, Hungary, 1037
- Károli Gáspár University of the Reformed Church in Hungary
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Self-referred and registered for a family constellation workshop with one of the therapists (clinical psychologist / psychiatrist) who were willing to collaborate with the researchers of the present study
Exclusion Criteria:
- Age under 18 years
- Currently suffers from a diagnosed mental disorder
- Participated actively (not merely as a "representative") in a family constellation intervention in the 12 months preceding baseline assessment
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
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Workshop participants
Participants of systemic / family constellation workshops
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Systemic / family constellation integrates elements from psychodrama, family sculpture, and spontaneous dramatizations of intra- and interpersonal processes, while spatially visualizing family dynamics.
Family constellations stimulate change through the following ways: 1) making visible the spatial arrangement of relationships within a conflictual system; 2) providing access to the insights of unrelated third parties regarding the sensations, feelings, and thoughts they experienced while representing family members within the constellation; and 3) making observable (from the outside) and experienceable (from within) the transformation of the problem constellation into the solution constellation [Hunger, Weinhold, Bornhäuser, Link, & Schweitzer, 2015].
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in scores on the Brief Symptom Inventory
Time Frame: Before, 1 month after and 6 months after the intervention
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A broad spectrum of psychopathological symptoms including somatization, obsession-compulsion, interpersonal sensitivity, depression, anxiety, hostility, phobic anxiety, paranoid ideation, and psychoticism
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Before, 1 month after and 6 months after the intervention
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Change in answers to ad hoc items developed for qualitative analysis
Time Frame: 1 and 6 months after the intervention
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These items are developed by the study authors to 1) screen for any potential adverse outcomes as a result of the intervention, 2) better understand the treatment goals of individuals participating in this form of therapy and how these relate to what they perceive as the outcome of the intervention
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1 and 6 months after the intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in scores on the Experience in Personal Social Systems Questionnaire
Time Frame: Before, 1 month after and 6 months after the intervention
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Assessment of how the members of a personal social system experience their situation within that system.
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Before, 1 month after and 6 months after the intervention
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Change in scores on the Patient Health Questionnaire Somatic Symptom Severity Scale (PHQ-15)
Time Frame: Before, 1 month after and 6 months after the intervention
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The PHQ-15 includes 15 somatic symptoms (headache, stomach pain, chest pain, dizziness, etc.) that account for more than 90% of symptoms seen in primary care (exclusive of upper respiratory symptoms)
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Before, 1 month after and 6 months after the intervention
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Change in scores on the SCOFF
Time Frame: Before, 1 month after and 6 months after the intervention
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The SCOFF is a brief screener to detect increased risk for eating disorders
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Before, 1 month after and 6 months after the intervention
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Change in scores on ad hoc items to assess behavioral and substance-related addictions
Time Frame: Before, 1 month after and 6 months after the intervention
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Items assess perceived problem severity with addictions
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Before, 1 month after and 6 months after the intervention
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Change in scores on the Meaning in Life Questionnaire (MLQ)
Time Frame: Before, 1 month after and 6 months after the intervention
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The MLQ assesses the perceived level of the presence and search for meaning in an individual's life
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Before, 1 month after and 6 months after the intervention
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Change in scores on the World Health Organization Wellbeing Index (WBI-5)
Time Frame: Before, 1 month after and 6 months after the intervention
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The WBI-5 captures the general well-being of the individuals
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Before, 1 month after and 6 months after the intervention
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Collaborators and Investigators
Collaborators
Investigators
- Study Director: Barna Konkoly Thege, PhD, Department of Psychiatry, Univeristy of Toronto
Publications and helpful links
General Publications
- Konkoly Thege B, Petroll C, Rivas C, Scholtens S. The Effectiveness of Family Constellation Therapy in Improving Mental Health: A Systematic Review. Fam Process. 2021 Jun;60(2):409-423. doi: 10.1111/famp.12636. Epub 2021 Feb 2.
- Weinhold J, Hunger C, Bornhauser A, Link L, Rochon J, Wild B, Schweitzer J. Family constellation seminars improve psychological functioning in a general population sample: results of a randomized controlled trial. J Couns Psychol. 2013 Oct;60(4):601-9. doi: 10.1037/a0033539. Epub 2013 Aug 19.
- Hunger C, Weinhold J, Bornhauser A, Link L, Schweitzer J. Mid- and long-term effects of family constellation seminars in a general population sample: 8- and 12-month follow-up. Fam Process. 2015 Jun;54(2):344-58. doi: 10.1111/famp.12102. Epub 2014 Sep 29.
- Hunger C, Bornhauser A, Link L, Schweitzer J, Weinhold J. Improving experience in personal social systems through family constellation seminars: results of a randomized controlled trial. Fam Process. 2014 Jun;53(2):288-306. doi: 10.1111/famp.12051. Epub 2013 Nov 19.
- Konkoly Thege B, Somogyi B, Szabo GS. The Effectiveness of Family Constellation Therapy in Reducing Psychopathological Symptoms in a Naturalistic Setting. Psychiatr Danub. 2022 Fall;34(3):497-505. doi: 10.24869/psyd.2022.497.
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
Other Study ID Numbers
- 325/2017/P
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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