Clinical Trials Directory

Trials / Completed

CompletedNCT06903104

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Institut de Cancérologie de Lorraine · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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

Interventions

TypeNameDescription
OTHERMindfulness closed programMAEva 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_TESTQuality of life evaluationThe assessment will be carried out at inclusion and after completion of the program.
DIAGNOSTIC_TESTPerceived Stress ScaleThe assessment will be carried out at inclusion and after completion of the program.
DIAGNOSTIC_TESTMultidimensional Psychological Flexibility InventoryThe assessment will be carried out at inclusion and after completion of the program.
OTHERsatisfaction questionnaire and semi-structured interviewThe assessments will be carried out after completion of the program.

Timeline

Start date
2025-03-13
Primary completion
2025-04-30
Completion
2025-09-13
First posted
2025-03-30
Last updated
2025-12-26

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT06903104. Inclusion in this directory is not an endorsement.