NCT06778109

Brief Summary

Medical doctor generally are exposed to several risks and pressures, it is not a case that several meta-analyses have shown high stress and anxiety level in these workers. Stress management represents a very important topic. Being a doctor means dealing with continous effort and arousal management to provide the best treatment through executive functions capacity. This is particularly true for younger medical trainees; that have also to learn how to deal with failure and the curve of learning. Hypnosis has been shown to be very effective at modulating executive functions and sympathovagal balance, with large effect in post traumatic stress disease (PTSD), anxiety and executive function modulation. Therefore, this study aim to investigate if hypnosis could be beneficial among medical trainees for managing negative thoughts related to work.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
26

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 29, 2024

Completed
18 days until next milestone

First Posted

Study publicly available on registry

January 16, 2025

Completed
21 days until next milestone

Study Start

First participant enrolled

February 6, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2025

Completed
Last Updated

February 18, 2026

Status Verified

February 1, 2026

Enrollment Period

2 months

First QC Date

December 29, 2024

Last Update Submit

February 13, 2026

Conditions

Keywords

stressdisorderhypnosis

Outcome Measures

Primary Outcomes (2)

  • Evaluation of the variations of the tonic and phasic component of the Electrodermal Activity (EDA,microSiemens) and Skin conductance response comparing pre and post-hypnosis (SCr/min)

    Evaluation of the variations of the tonic and phasic component of the Electrodermal Activity (EDA,microSiemens) and Skin conductance response comparing pre and post-hypnosis (SCr/min)

    T0) Within 3 minutes from electrodes application (at baseline), T1) within 3minute after a negative memory (w/o hypnosis), T2) within 3minutes after a positive memory, T3) within 3minutes after recalling the negative memory (after hypnosis application)

  • Evaluation of the executive performance comparing pre- and post-hypnosis through Tower of London-Revised (TOL-R) (number of correct responses)

    Evaluation of the executive performance comparing pre- and post-hypnosis through Tower of London-Revised (TOL-R) (number of correct responses)

    Within 3 minutes from the first negative memory (without hypnosis) and then, within 3 minutes from the negative memory (with hypnosis)

Secondary Outcomes (2)

  • Evaluation of the variations of psychological stress response to a negative memory related to work between pre and post hypnosis on a scale from 0 to 10

    Within 3 minutes from the first negative memory (without hypnosis) and then, within 3 minutes from the negative memory (with hypnosis)

  • Evaluation of the Heart rate variability (HRV) comparing pre and post-hypnosis (ms)

    T0) Within 3 minutes from electrodes application (at baseline), T1) within 3minute after a negative memory (w/o hypnosis), T2) within 3minutes after a positive memory, T3) within 3minutes after recalling the negative memory (after hypnosis application)

Study Arms (2)

Hypnosis and negative memory (n. 26)

EXPERIMENTAL

T0) basal evaluation of physiological data T1) evaluation of physiological data after recollecting a negative memory for 3 minutes T2) evaluation of physiological data after that a brief session of hypnosis (performed with positive memories) T3) evaluation of physiological data recolling, for the second time, the negative memory.

Behavioral: Experimental: Hypnosis and negative memory

Control group (n. 23)

SHAM COMPARATOR

Active control group con breath-focused attention. Allocation: Non-randomized

Behavioral: Sham Comparator: Control group

Interventions

Arm Description: T0) basal evaluation of physiological data T1) evaluation of physiological data after recollecting a negative memory for 3 minutes T2) evaluation of physiological data after that a brief session of hypnosis (performed with positive memories) T3) evaluation of physiological data recolling, for the second time, the negative memory.

Hypnosis and negative memory (n. 26)

Arm Description: Active control group con breath-focused attention. Allocation: Non-randomized

Control group (n. 23)

Eligibility Criteria

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

You may qualify if:

  • age \> 18 years old,
  • being medical doctor or at first year of residency in Anesthesiology
  • obtained written informed consent

You may not qualify if:

  • Neurological issues affecting stress responses
  • Diabetes
  • Cardiovascular conditions (i.e., hypertension, orthostatic hypotension etc)
  • Being under psychiatric medications
  • Psychological or psychiatric diseases

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Istituto di Anestesia e Rianimazione

Padua, Italy, 35126, Italy

Location

University of Padova

Padua, PD, 35126, Italy

Location

Related Publications (1)

  • Queirolo L, Boscolo A, Cracco T, Moscardi O, Facco E, Zanette G, Stellini E, Navalesi P. Hypnosis reshapes multilevel stress response and enhances executive performance in stressed medical students. Sci Rep. 2026 Feb 26;16(1):8844. doi: 10.1038/s41598-026-40770-6.

MeSH Terms

Conditions

Stress Disorders, TraumaticDisease

Condition Hierarchy (Ancestors)

Trauma and Stressor Related DisordersMental DisordersPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

December 29, 2024

First Posted

January 16, 2025

Study Start

February 6, 2025

Primary Completion

April 1, 2025

Study Completion

April 1, 2025

Last Updated

February 18, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

Locations