Behavior Clinical Trial
— MEMOREMOfficial title:
The Effects of Mindfulness Meditation on Brain Metabolism in the Limbic Regions Studied by Magnetic Resonance Spectroscopy; Correlations With the Memory Performance and Episodic Metamemetory of Students.
Stress reduction methods based on mindfulness meditation have been experiencing significant growth in various fields of society over the past twenty years. In the case of students, scientific work has shown that mindfulness training has a positive effect on their mental health and possibly on their academic performance through improved attention and memory. The effect of metamemory ("knowing what you know and what you don't know"), which plays an important part in students memorization and academic success, has not yet been explored. Changes in brain structure have been noted by MRI in some regions after several weeks of mindfulness training, but very few studies have yet looked at changes in brain metabolism that can be observed by the spectrocopy technique. The investigators will conduct a prospective randomized study with overall 30 female speech therapists student that will be enrolled and assigned randomly to two groups, in a 1:1 ratio : one groupe that will benefit from mindfulness training and the other group that will benefit from another method of stress reduction based on muscular relaxation. The programs will extend over 6 weeks with session of 2h30 per week in groups having personnal daily exercices (30-40' per day). During the 3 weeks leading up to and the 2 weeks following the program, students will take tests exploring memory and metamemory, complete mental health questionnaires, and have a magnetic resonance imaging with spectroscopic analysis.
Status | Not yet recruiting |
Enrollment | 30 |
Est. completion date | January 30, 2024 |
Est. primary completion date | January 30, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 30 Years |
Eligibility | Inclusion Criteria: Female - Right-handed - = 18 years old - Affiliated to a social security scheme - Written consent signed by the participan Exclusion Criteria: - Inability to complete the entire study programme - Previous participation in an MBSR or MBCT programme - Current neurological pathology - Current psychiatric pathology, score = 3 on the PHQ-4 self-questionnaire - Previous or ongoing psychological or psychiatric treatment - Previous or current psychotropic treatment - Usual contraindications to brain MRI (including claustrophobia, ocular metallic foreign body, pacemaker, neurostimulator, cochlear implants (or non-removable electronic medical equipment), old generation heart valves, vascular clips previously implanted on a cranial aneurysm). - Pregnancy - During the exclusion period of a clinical research study - Under legal protection or deprived of liberty. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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University Hospital, Tours |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from Baseline in Glumatate concentrations (mM) at 8 Weeks | Glumatate concentrations (mM) are measured by magnetic resonance spectrocopy in left hippocampal formation | baseline and 8 weeks | |
Secondary | Change in left hippocampal formation volumes (mm3) measured on MRI 3D T1w sequence | baseline and 8 weeks | ||
Secondary | Change in right amygdala volumes (mm3) measured on MRI 3D T1w sequence | baseline and 8 weeks | ||
Secondary | Change in posterior cingulate volumes (mm3) measured on MRI 3D T1w sequence | baseline and 8 weeks | ||
Secondary | Chang in overall brain volume measured on MRI 3D T1w sequence | baseline and 8 weeks | ||
Secondary | Change in score the Feeling of knowing task (FOK task) | FOK task for episodic memory performance includes 4 distincts steps : (1) a learning phase of a 60 pairs of words, (2) a cued recall phase (number of correct recalls /60 ; number of incorrect recalls /60), (3) feeling of knowing phase, (4) recognition phase (number of correct recognition /60 ; number of incorrect recognition /60) | baseline and 8 weks | |
Secondary | Change in score of the Trail Making Test (TMT) | TMT consists of two parts. In the first part (A), the subject must connect with a pen in the correct order 25 numbers from 1 to 25, which are distributed randomly.
In the second part (B), the subject must connect with a pencil in the correct order an alternation of 13 numbers from 1 to 13 and 12 letters from A to L, which are also distributed randomly. The time in seconds to complete each part is measured. |
baseline and 8 weeks | |
Secondary | Change in score of Stroop test | The test includes 3 phases. In each one, participant have to give maximum of correct answer.
Score ranges from 0 to 100 for each phase |
baseline and 8 weeks | |
Secondary | Change in score of N-Back test | Number of correct answer (yes or no). Total score /23 | Baseline and at 8 weeks | |
Secondary | Change in score of attentional network test (ANT) | Test (ANT) is a computerized testing measure that analyses the three components of attention network : alerting, orienting, executive control.
Each of these three attention components is measured in time. |
baseline and 8 weeks | |
Secondary | Change in score of the number memory task | Number memory score in direct order, ranges from 0 to 16. Number memory score in indirect order, ranges from 0 to 16 | baseline and 8 weeks | |
Secondary | Change in score of the Hospital Anxiety and Depression Scale (HADS) | Anxio-depressive symptomatology based on the HADS score. The questionnaire is divided in two subscales, one for anxiety and one for depression. Each subscore ranges from 0 to 21. Scores greater than or equal to 11 on either scale indicate anxious or depressive symptomatology. | baseline and 8 weeks | |
Secondary | Change in score of the Perceived Stress Scale (PSS) | Anxio-depressive symptomatology based on the PSS score. The total score ranges from 0 to 40. Higher scores reflect greater stress level. | baseline and 8 weeks | |
Secondary | Change in score of the Columbia Suicide Severity Rating Scale (C-SSRS) | Evaluation of suicidality through the C-SSRS. The suicidal ideation severity subscale ranges from 1 to 5 (with higher number indicating more severe ideation). The intensity of ideation subscale includes 5 questions each one ranging from 1 to 5 (with higher number indicating more intense ideation). The suicidal behavior subscale includes 4 yes/no questions. The suicidal behavior lethality subscale inquires about the level of actual or potential medical damage. | baseline and 8 weeks | |
Secondary | Change in score of the World Health Organization Quality of Life (WHOQOL) | Quality of life based on the WHOQOL score. The total score ranges from 0 to 100. Higher scores reflect better health. | baseline and 8 weeks |
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