The goal of this clinical trial is to evaluate whether participation in 12 Qi Gong sessions (intervention group), compared with usual care without Qi Gong (control group), reduces dissociative symptoms, as measured by the Dissociative Experience Scale-II (DES-II), between T0 and T1, in outpatients hospitalized for psychiatric disorders related to aversive experiences during childhood.
The main questions it aims to answer are:
\- a) To assess whether participation in the Qi Gong program leads to a reduction in symptoms related to complex trauma, b) To assess whether participation in the Qi Gong program leads to an increase in the level of mindfulness c) To explore whether the effect of the Qi Gong program on reducing dissociative symptoms varies according to participants' baseline level of dissociation (Dissociative Experiences Scale-II ) d) To explore whether the effect of the Qi Gong program on reducing dissociative symptoms is sustained over time e) To explore the experiences of patients who participated in the Qi Gong sessions following the intervention.
This is a randomized controlled trial with parallel groups:
* Intervention group: participation in 12 Qi Gong sessions led by a trained professional, in addition to standard care * Control group: standard care, without access to Qi Gong sessions during the study period.
Participants will be required to:
* complete 3 questionnaires (DES-II, ITQ, MAAS) * attend one Qi Gong session per week for 12 weeks (including a group debriefing) or receive standard care at a medical-psychological center (without Qi Gong) * complete the same questionnaires (DES-II, ITQ, MAAS) after the 12 weeks * complete the DES-II questionnaire 2 months later
18 years of age or older
A score above the 10th percentile on the Dissociative Experience Scale-II (DES-II)
A score above 2 on the ACE scale (Adverse Childhood Experiences by Felitti et al., 1998)
A medical certificate attesting to the participant's fitness to practice Qigong
In a suicidal crisis
In a hallucinatory crisis
Experiencing a major depressive episode
Unstabilized
Parallel
Qi-Gong
Other intervention1 Qi Gong session per week for 12 weeks
Reduction in dissociative symptoms
Symptoms of dissociation, as measured by the Dissociative Experiences Scale-II (DES-II), will be compared between the intervention group (Qi Gong sessions) and the control group (usual care without Qi Gong).
To assess whether participation in the Qi-Gong program leads to a reduction in symptoms related to complex trauma
Change in mean ITQ scores between T1 and T0 (T1-T0); this change will be calculated for each participant.
To assess whether participation in the Qigong program leads to an increase in the level of mindfulness
Change in mean MAAS scores between T1 and T0 (T1-T0); this change will be calculated for each participant.
To investigate whether the effect of the Qigong program on reducing dissociative symptoms varies depending on participants' initial level of dissociation
Change in the mean DES-II score between T1 and T0 (T1-T0), according to the baseline level of dissociation, as measured by the DES-II. This change will be calculated for each participant.
To investigate whether the effect of the Qigong program on reducing dissociative symptoms persists over time
Change in the mean DES-II score between T2 and T1 (T2 - T1). This change will be calculated for each participant.
To explore the experiences of patients who participated in Qi Gong sessions following the intervention.
The experiences of patients who participated in Qi Gong sessions were assessed through focus groups held after each Qi Gong session, in the form of a debriefing,
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