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Impact of ERCS on Perceived Stress in Patients Hospitalized in the Post-resuscitation Rehabilitation Service

Impact of Energy Resonance by Skin Stimulation on Perceived Stress in Patients Hospitalized in the Post-resuscitation Rehabilitation Service

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07422077
Acronym
IRESC
Enrollment
38
Registered
2026-02-19
Start date
2025-12-08
Completion date
2027-09-08
Last updated
2026-02-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress Disorders, Post-Traumatic

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

Interventions

OTHERERCS sessions

Two ERCS sessions spaced one week apart, on Day 0 and Day 7

Sponsors

Hôpital Européen Marseille
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Difference in the level of perceived stress by the patient before and immediately after the second RESC session (two sessions on day 0 and day 7), measured using a Visual Analog Scale (VAS).Day 0 and day 7

Secondary

MeasureTime frame
Daily evolution of perceived stress (VAS) between Day 0 and Day 7Day 0 and day 7
Difference in pain (VAS) between, before and after each sessionDay 0 and day 7
Measurement in clinical parameters before and after each session (respiratory rate breaths per minute/bpm; heart rate beats per minute/bpm; blood pressure millimeters of mercury, mmHg; oxygen saturation percentage, %)Day 0 and day 7
Anxiety score (COVI scale) before and after each sessionDay 0 and day 7
Measurement of the patient's physical symptoms during the session using a binary scale for each symptom at the end of each RESC sessionDay 0 and day 7
Duration of each ERCS sessionDay 0 and day 7

Countries

France

Contacts

CONTACTMyriam BENNANI
m.bennani@hopital-europeen.fr0413428351

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026