- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05314166
Impact of Face-to-face Meditation on Non-attachment to Self and Identity Threat (MEDIT-PRESENT)
Meditation is widely recognized for its benefits on both physical and psychological health and more particularly on the prevention of depression relapse. However, despite a lot of literature showing its efficacy, the mechanisms of action underlying its benefits have yet to be specifically identified and empirically tested.
to understand these mechanisms actions, it is essential to distinguish meditative practices. Three different categories of meditation can be distinguished: "Attention Family", "Constructive Family" and "Deconstructive Family" with specific effects for each.
Study Overview
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- male or female
- aged of 18 and more
- without diagnosed psychiatric pathology
- not practicing meditation
- agreeing to participate in the study
Exclusion Criteria:
- less than 18 years old
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: "focused attention" group
"focused attention" group: adult subjects practicing face-to-face focused attention meditation.
|
Description: meditation practice
|
|
Active Comparator: "contemplation" group
"contemplation" group: adult subjects practicing face-to-face contemplation meditation.
|
Description: meditation practice
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
non-attachment to the self
Time Frame: week 6
|
Non-attachment to the self evaluated using Adult Self-transcendence Inventory (ASTI). ASTI is composed of 10 items. Each item is coded from 1 (totally disagree) to 7 (totally agree) by comparing how they see life at the time of the questionnaire compared to the last 5 years. The overall score ranges from 10 to 70 points. |
week 6
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Identity threat
Time Frame: week 6
|
Identity threat evaluated using Cognitive Appraisal Scale (ECP).
ECP is composed of 10 items.
Each item is coded from 1 (totally disagree) to 6 (totally agree).
The overall score ranges from 6 to 60 points
|
week 6
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2022-RIPH_004_MEDIT-ENPRESENT
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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