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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHôpital Européen Marseille

About this trial

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

This trial does not accept healthy volunteers

Qualifiers

Aged ≥ 18 years

Hospitalized adults in a Post-Intensive Care Rehabilitation Unit (SRPR)

Having given free and informed written consent

Disqualifiers

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.

Trial design

Design model

Single group

Treatments tested in this trial

  • ERCS sessions

    Other intervention

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

Treatment groups

38 Participants
are divided into 1 treatment group
Group A: Patients hospitalized in the post-ICU rehabilitation service.Other 1 intervention

Trial outcomes

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

Other outcomes

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