Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04701723

Interest of Cardiac Coherence in the Prevention of Chronic Post-traumatic Stress Disorder: Pilot Study

Led by Centre Hospitalier Universitaire de la Réunion · Updated on 2026-03-12

44

Participants Needed

1

Research Sites

301 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

ThThe aim of this study is to determinate the potential benefits of a respiratory training program (cardiac coherence, CC) in patients suffering from acute stress disorder, after a potentially traumatic event. Using this method is supposed to prevent the onset of chronic post traumatic stress disorder after 3 months. This pilot study will help to determinate the need of developing this kind of complementary and alternative program, and will also provide knowledge about the feasibiility and acceptability of this program for the patients.

CONDITIONS

Official Title

Interest of Cardiac Coherence in the Prevention of Chronic Post-traumatic Stress Disorder: Pilot Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients seen at medico-psychological emergency cell
  • Patients with an acute stress disorder diagnosed by DSM-5
  • Patients who have experienced a potentially traumatic event within the last 3 to 15 days (victim or witness)
  • Patients able to read and write in French
  • Person affiliated with or beneficiary of a social security scheme
  • Person who agrees to participate in the study
Not Eligible

You will not qualify if you...

  • Patients with respiratory conditions preventing cardiac coherence training
  • Patients currently practicing or having practiced a regular respiratory control technique within the last 6 months
  • Patients taking beta-blockers, betamimetics, anti-arrhythmics, opioids, or antidepressants
  • Patients with a pacemaker or severe cardiac illness
  • Patients with non-stabilized psychiatric disorder at inclusion
  • Patients taking benzodiazepines unable to stop within one week after inclusion
  • Patients with addiction
  • Patients with cognitive deficits
  • Patients under guardianship, curatorship, or judicial supervision

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Etablissement Public de Santé Mentale de La Réunion

Saint-Paul, Reunion, 97460

Actively Recruiting

Loading map...

Research Team

E

Emilie TECHER

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here