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NCT Number: NCT07422077

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

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

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hôpital Européen Marseille

Marseille, France

Location status: Recruiting

Location contact

Gina BOUVIER

PRINCIPAL_INVESTIGATOR

Myriam BENNANI

CONTACT

[email protected]

0413428351

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

ERCS sessions

Other

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

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).

    Time frame: Day 0 and day 7

Secondary outcomes

  1. Daily evolution of perceived stress (VAS) between Day 0 and Day 7

    Time frame: Day 0 and day 7

  2. Difference in pain (VAS) between, before and after each session

    Time frame: Day 0 and day 7

  3. 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, %)

    Time frame: Day 0 and day 7

  4. Anxiety score (COVI scale) before and after each session

    Time frame: Day 0 and day 7

  5. Measurement of the patient's physical symptoms during the session using a binary scale for each symptom at the end of each RESC session

    Time frame: Day 0 and day 7

  6. Duration of each ERCS session

    Time frame: Day 0 and day 7

Study contacts

Contact information is provided by the study sponsor or research team.

Myriam BENNANI

CONTACT

[email protected]

0413428351

Sponsors and collaborators

Lead sponsor

Hôpital Européen Marseille

Other

Registry information

Official study title

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

Acronym: IRESC

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Feb 19, 2026
Registry last updated
Feb 19, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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