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Acceptability and Feasibility of a Stress Prevention Program Based on Meditation and Acceptance and Commitment Therapy for Staff at a Cancer Center

NCT06903104 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2025-12-26

No results posted yet for this study

Summary

The MAEva program seems to meet the challenges of implementing meditation for cancer care workers. As part of our Quality of Life and Working Conditions initiative, the investigator decided to offer it to staff at our Cancer Center. The MAEva program is delivered in a closed format: participants commit to following, as far as possible, the three sessions of the program - one session per week for 3 weeks. During the sessions, it will be proposed to train meditative practices and three different themes will be addressed (one theme per session): Meditation, Acceptance and Commitment to values.

Before and after the program, participants will complete a quality of life evaluation, a perceived stress scale, and a questionnaire to assess psychological flexibility.

At the end of the program, each participant will be asked to complete a satisfaction questionnaire and a semi-directive interview, by videoconference, or by telephone in the event of digital impossibility with voice recording, to enable a qualitative analysis.

Conditions

  • Employees at a Hospital

Interventions

OTHER

Mindfulness closed program

MAEva program will be proposed with meditative practices and three different themes will be addressed (one theme per session): Meditation, Acceptance and Commitment to values.

DIAGNOSTIC_TEST

Quality of life evaluation

The assessment will be carried out at inclusion and after completion of the program.

DIAGNOSTIC_TEST

Perceived Stress Scale

The assessment will be carried out at inclusion and after completion of the program.

DIAGNOSTIC_TEST

Multidimensional Psychological Flexibility Inventory

The assessment will be carried out at inclusion and after completion of the program.

OTHER

satisfaction questionnaire and semi-structured interview

The assessments will be carried out after completion of the program.

Sponsors & Collaborators

  • Institut de Cancérologie de Lorraine

    lead OTHER

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-03-13
Primary Completion
2025-04-30
Completion
2025-09-13

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06903104 on ClinicalTrials.gov