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OpenTrials
Completed

NCT Number: NCT06056414

Study of Anxiety After a Session of Energy Resonance by Cutaneous Stimulation

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Centre Henri Becquerel

Rouen, France

Who can participate

Healthy volunteers accepted: No

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

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

Treatment and study plan

Energy Resonance by Cutaneous Stimulation

Other

Energy Resonance by Cutaneous Stimulation session

Primary outcomes

  1. Evaluation of the reduction in ANXIETY STATE

    Time frame: 1 day

    Evaluation of anxiety before and after RESC session using Spielberger scale

Secondary outcomes

  1. Evaluation of the reduction in ANXIETY STATE

    Time frame: 3 days

    Evaluation of anxiety before and after RESC session using Spielberger scale

  2. Evaluation of the reduction in ANXIETY STATE

    Time frame: 7 days

    Evaluation of anxiety before and after RESC session using Spielberger scale

Sponsors and collaborators

Lead sponsor

Centre Henri Becquerel

Other

Registry information

Official study title

Study of the Reduction of Anxiety After a Session of Energy Resonance by Cutaneous Stimulation in the Management of Patients Requiring Breast Macrobiopsy.

Acronym: MBRESC

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Sep 28, 2023
Registry last updated
Jan 2, 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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