Actively Recruiting
WELL-being Improvement Following Sophrology Practice
Led by University Hospital, Clermont-Ferrand · Updated on 2024-11-29
60
Participants Needed
1
Research Sites
128 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Stress and psychosocial risks are a major public health problem.Sophrology is a psycho-corporal method exclusively verbal and non-tactile used as a therapeutic technique. It combines a set of techniques that will act both on the body and on the mind through breathing exercises, muscle relaxation and mental imagery (or visualization). It allows to find a state of well-being and to activate all physical and psychological potential in order to acquire a better knowledge of oneself. Sophrology demonstrated some benefits on symptoms of patients. However, these approaches have never been evaluated with a prolonged follow-up of several months, with biological measures or with adjustments according to the levels of mastery of sophrology. This project proposes to evaluate the effects of sophrology practice. The investigators aim to evaluate both subjective and objective measures of stress.
CONDITIONS
Official Title
WELL-being Improvement Following Sophrology Practice
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Able to give informed consent to participate in the research
- Committed to respecting the inclusion criteria of their group
- For sophrology practitioners: practice sophrology at least once a week using the dynamic relaxation method
- For non-practitioners: do not practice sophrology during the follow-up and inform the investigator if this changes
You will not qualify if you...
- Being a protected person including minors, pregnant or breastfeeding women, those under guardianship, curatorship, deprived of liberties, or with legal safeguards
- Refusal to participate in the study
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
CHU Clemront-Ferrand
Clermont-Ferrand, France
Actively Recruiting
Research Team
L
Lise Laclautre
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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