NCT07422077 Impact of ERCS on Perceived Stress in Patients Hospitalized in the Post-resuscitation Rehabilitation Service
| NCT ID | NCT07422077 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Hôpital Européen Marseille |
| Condition | Stress Disorders, Post-Traumatic |
| Study Type | INTERVENTIONAL |
| Enrollment | 38 participants |
| Start Date | 2025-12-08 |
| Primary Completion | 2027-06-08 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 38 participants in total. It began in 2025-12-08 with a primary completion date of 2027-06-08.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Surviving an intensive care unit hospitalization (ICU) can be the beginning of a long rehabilitation journey, hindered by symptoms of stress, PTSD, anxiety, and depression. In order to improve the care of these patients, it's essential to explore effective non-pharmacological approaches to reduce stress. Many non-drug techniques are being developed to alleviate the physical and psychological pain of patients. Energy Resonance by Skin Stimulation (ERCS) is a noninvasive method of soothing and supporting the patient. This technique is based on the energetic principles of traditional Chinese medicine. It relies on a "listening contact" through the stimulation of cutaneous points to create resonance and transmit vibrational and wave messages in the tissues. ERCS has various applications, whether for the management of acute or chronic pain, emotional disorders such as fear, anxiety, and depression. Our study aims to assess the effects of ERCS on the perceived stress of patients hospitalized in the post-ICU rehabilitation service. By demonstrating its potential impact on both physical and psychological recovery, this research could support the integration of RESC into care protocols and open new perspectives for stress management in hospital settings
Eligibility Criteria
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.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07422077 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Stress Disorders, Post-Traumatic. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07422077 currently recruiting?
Yes, NCT07422077 is actively recruiting participants. Contact the research team at m.bennani@hopital-europeen.fr for enrollment information.
Where is the NCT07422077 trial being conducted?
This trial is being conducted at Marseille, France.
Who is sponsoring the NCT07422077 clinical trial?
NCT07422077 is sponsored by Hôpital Européen Marseille. The trial plans to enroll 38 participants.