ClinicalTrials.gg
Not yet recruitingNCT07670663Qi-TUpdated Sep 23, 2026

Effects of a Qi Gong Program on Dissociative Symptoms in Patients Who Have Experienced Childhood Trauma

An interventional study of Qi-Gong in Psychiatry, sponsored by Centre Hospitalier Universitaire de la Réunion. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-23.

Sponsored by Centre Hospitalier Universitaire de la Réunion · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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 : Dissociative Experience Scale-II (DES-II), International Trauma Questionnaire (ITQ) , Mindfull Attention Awarness Scale (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
02

Conditions studied

  • Psychiatry

Keywords

  • dissociative symptoms
  • childhood trauma
  • Qi- Qong
03

In context

Lead sponsor

Centre Hospitalier Universitaire de la Réunion is the lead sponsor of 141 studies on the registry; 37 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 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
  • A person enrolled in or receiving benefits from a social security program
  • Free, informed, and written consent signed by the participant and the investigator (no later than the day of enrollment and prior to any examination required by the study).

Exclusion criteria

Exclusion Criteria:

  • In a suicidal crisis
  • In a hallucinatory crisis
  • Experiencing a major depressive episode
  • Unstabilized
  • Pregnant women
  • Those who do not understand French
  • Under guardianship or conservatorship
  • Under judicial protection
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
90 participants (estimated)

Study arms

  • Experimental
    Qi-gong

    One Qi Gong session per week for 12 weeks, in groups of six, led by a certified professional.

    Other: Qi-Gong

  • No intervention
    Routine Care (without Qi Gong)

    Routine care at a medical-psychological center (appointments with psychologists, doctors, and registered nurses scheduled as part of standard care), excluding participation in Qi Gong sessions

Interventions

  • OtherQi-Gong

    1 Qi Gong session per week for 12 weeks

06

What researchers measure

Primary outcomes

  1. Change 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).

    Time frame: 3 months after enrollment

  2. To assess whether participation in the Qi-Gong program leads to a reduction in symptoms related to complex trauma

    Change in International Trauma Questionnaire scores between T1 and T0 (T1-T0); The DES-II is a validated 28-item self-report questionnaire used to assess the intensity and frequency of dissociative experiences. It is based on the concept of a dissociative continuum ranging from mild forms (absorption) to more severe forms (amnesia, depersonalization, derealization). Participants rate each item on a Likert scale ranging from 0% to 100%, indicating how often they experience each described phenomenon. The final score is the average of the responses to all 28 items (ranging from 0 to 100%). The higher the score, the more "dissociated" the person is.

    Time frame: 3 months after enrollment

Secondary outcomes

  1. To assess whether participation in the Qigong program leads to an increase in the level of mindfulness

    Change in Mindfull Attention Awarness Scale (MAAS) scores between T1 and T0 (T1-T0); The MAAS (Brown \& Ryan 2003) is a 15-item questionnaire scored on a 6-point Likert scale ranging from "Almost Always" (1) to "Almost Never" (6). The total score therefore ranges from 15 to 90. The higher the score, the more frequently the person is mindful.

    Time frame: 3 months after enrollement

  2. 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. The DES-II is a validated 28-item self-report questionnaire used to assess the intensity and frequency of dissociative experiences. It is based on the concept of a dissociative continuum ranging from mild forms (absorption) to more severe forms (amnesia, depersonalization, derealization). Participants rate each item on a Likert scale ranging from 0% to 100%, indicating how often they experience each described phenomenon. The final score is the average of the responses to all 28 items (ranging from 0 to 100%). The higher the score, the more "dissociated" the person is.

    Time frame: 3 months after enrollment

  3. 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). The DES-II is a validated 28-item self-report questionnaire used to assess the intensity and frequency of dissociative experiences. It is based on the concept of a dissociative continuum ranging from mild forms (absorption) to more severe forms (amnesia, depersonalization, derealization). Participants rate each item on a Likert scale ranging from 0% to 100%, indicating how often they experience each described phenomenon. The final score is the average of the responses to all 28 items (ranging from 0 to 100%). The higher the score, the more "dissociated" the person is.

    Time frame: 5 months after enrollement

  4. 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,

    Time frame: 3 month after enrollment

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07670663
Responsible party
Sponsor
First posted
Jun 26, 2026
Start date
Sep 2026 (estimated)
Primary completion
Jan 2029 (estimated)
Completion
Mar 2029 (estimated)
Last update
Sep 23, 2026

Study contacts

Olivier Martinez, Mr
Contact
olivier.martinez@chu-reunion.fr
0262 262570169

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion