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Study of Anxiety After a Session of Energy Resonance by Cutaneous Stimulation (MBRESC)

C

Centre Henri Becquerel

Status

Completed

Conditions

Breast Neoplasm

Treatments

Other: Energy Resonance by Cutaneous Stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT06056414
CHB23.02

Details and patient eligibility

About

Performing a breast macrobiopsy can be extremely delicate and anxiety-provoking. It can have an impact on the course of future examinations.

Patients' emotional feelings also have a definite impact on the nursing staff. The purpose of the MBRESC study is to evaluate Energy Resonance by Cutaneous Stimulation , a manual acupressure technique, in the management of anxiety prior to breast macrobiopsy.

Enrollment

57 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient has received full information on the organization and purpose of the research, and has signed an informed consent form.
  • Patient over 18 years of age
  • Patient undergoing a diagnostic breast macrobiopsy for suspected breast cancer
  • Patient undergoing a macro breast biopsy for the first time
  • Patient affiliated to or benefiting from a social security schem

Exclusion criteria

  • Patient with a history of breast cancer or other pathologies requiring invasive procedures
  • Patient with several lesions to be biopsied
  • Patient with psychiatric pathology
  • Patient under anxiolytic or psychotropic treatment initiated in the month before the breast macrobiopsy

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

57 participants in 1 patient group

Energy Resonance by Cutaneous Stimulation
Experimental group
Description:
one Energy Resonance by Cutaneous Stimulation session performed before macrobiopsy
Treatment:
Other: Energy Resonance by Cutaneous Stimulation

Trial contacts and locations

1

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Central trial contact

Celine Lemaire; Doriane Richard

Data sourced from clinicaltrials.gov

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