Energy Resonance by Skin Stimulation to reduce stress after ICU hospitalization

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The study delivers repeated ERCS sessions—a nonpharmacological touch-based technique rooted in energetic principles of traditional Chinese medicine—to adults hospitalized in a post‑resuscitation rehabilitation unit. Participants receive ERCS as part of their rehabilitation and researchers measure changes in patients' perceived stress using standard patient‑reported measures. The intervention is noninvasive and focuses on stimulation of cutaneous points to induce resonance and calming sensations in tissues. Outcomes will compare stress levels before and after the ERCS course to determine short‑term effects on emotional recovery.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Aged ≥ 18 years
* Hospitalized adults in a Post-Intensive Care Rehabilitation Unit (SRPR)
* Having given free and informed written consent

Exclusion Criteria:

* Pregnant or breastfeeding woman
* Persons deprived of their liberty by a judicial or administrative decision.
* Persons who are subject to a legal protection measure or who are unable to express their consent.

Where it's running

• Hôpital Européen Marseille
  Marseille, France Recruiting

Study contacts

• Study coordinator: Myriam BENNANI
• Email: m.bennani@hopital-europeen.fr
• Phone: 0413428351

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.