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MindOb: A 12-month Computerized Mindfulness-based Intervention for Obese Individuals

NCT02571387 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2018-12-26

No results posted yet for this study

Summary

The purpose of this study is to evaluate the efficacy of a daily 12-month computerized mindfulness-based intervention in obese patients diagnosed with Binge Eating Disorder (BED) on: impulsive eating, motivation toward exercise, and weight loss.

Conditions

Interventions

BEHAVIORAL

Mindfulness-based intervention

BEHAVIORAL

Sham meditation

Sponsors & Collaborators

  • Hospital Ambroise Paré Paris

    collaborator OTHER

  • Nestlé Foundation

    collaborator OTHER

  • University of Paris 5 - Rene Descartes

    lead OTHER

Principal Investigators

  • Sébastien Czernichow, Pr · Hospital Ambroise Paré Paris

  • Cécile Flahault, PhD · University Paris 5 - Rene Descartes

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-31
Primary Completion
2019-10-31
Completion
2019-10-31

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

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 NCT02571387 on ClinicalTrials.gov