Impact of ERCS on Perceived Stress in Patients Hospitalized in the Post-resuscitation Rehabilitation Service
IRESC
Impact of Energy Resonance by Skin Stimulation on Perceived Stress in Patients Hospitalized in the Post-resuscitation Rehabilitation Service
1 other identifier
interventional
38
1 country
1
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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Dec 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 1, 2025
CompletedStudy Start
First participant enrolled
December 8, 2025
CompletedFirst Posted
Study publicly available on registry
February 19, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 8, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 8, 2027
February 19, 2026
February 1, 2026
1.5 years
December 1, 2025
February 18, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
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 Outcomes (6)
Daily evolution of perceived stress (VAS) between Day 0 and Day 7
Day 0 and day 7
Difference in pain (VAS) between, before and after each session
Day 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 session
Day 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 session
Day 0 and day 7
- +1 more secondary outcomes
Study Arms (1)
Patients hospitalized in the post-ICU rehabilitation service.
OTHERInterventions
Two ERCS sessions spaced one week apart, on Day 0 and Day 7
Eligibility Criteria
You may qualify if:
- Aged ≥ 18 years
- Hospitalized adults in a Post-Intensive Care Rehabilitation Unit (SRPR)
- Having given free and informed written consent
You may not qualify if:
- 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 the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hôpital Européen Marseille
Marseille, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 1, 2025
First Posted
February 19, 2026
Study Start
December 8, 2025
Primary Completion (Estimated)
June 8, 2027
Study Completion (Estimated)
September 8, 2027
Last Updated
February 19, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share