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Pain of Patients, Suffering of Caregivers: Evaluation of the Benefit of Full Consciousness Meditation in Oncology

Not Applicable
Completed
Conditions
Cancer
Pain
Interventions
Behavioral: Meditation
Registration Number
NCT04410185
Lead Sponsor
Centre Francois Baclesse
Brief Summary

The study is based on the realization of a meditation program associating patients, caregivers and control subjects

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
31
Inclusion Criteria

Not provided

Exclusion Criteria

For all participants

  • Participant with significant vulnerability factors dependence on alcohol and drugs, severe depression, severe social anxiety, recent mourning etc.).
  • Participant who cannot submit to the follow-up of the trial for geographic, social or psychopathological reasons

For patients

  • Very advanced stage of cancer disease with life-threatening commitment,
  • Participant deprived of liberty or under guardianship

For control subjects

  • Nursing staff, regardless of their place of practice

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
MEDITATIONMeditationMeditation sessions will take place over 12 weekly sessions of 1.5 hours. A retreat (3 hours) will be realized after the 9th session
Primary Outcome Measures
NameTimeMethod
Evaluate the adherence of all participants to the full meditation program3 months after the beginning of program

Proportion of participants adhering to the full meditation program (13 sessions)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Centre François Baclesse

🇫🇷

Caen, France

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