NCT07422077

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
38

participants targeted

Target at P25-P50 for not_applicable

Timeline
15mo left

Started Dec 2025

Geographic Reach
1 country

1 active site

Status
recruiting

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

Study Progress30%
Dec 2025Sep 2027

First Submitted

Initial submission to the registry

December 1, 2025

Completed
7 days until next milestone

Study Start

First participant enrolled

December 8, 2025

Completed
2 months until next milestone

First Posted

Study publicly available on registry

February 19, 2026

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 8, 2027

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 8, 2027

Last Updated

February 19, 2026

Status Verified

February 1, 2026

Enrollment Period

1.5 years

First QC Date

December 1, 2025

Last Update Submit

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.

OTHER
Other: ERCS sessions

Interventions

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

Patients hospitalized in the post-ICU rehabilitation service.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

MeSH Terms

Conditions

Stress Disorders, Post-Traumatic

Condition Hierarchy (Ancestors)

Stress Disorders, TraumaticTrauma and Stressor Related DisordersMental Disorders

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

Locations