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Mindfulness-Based Eating Training for Obesity (MB-EAT Trial)
N/A
Waitlist Available
Led By Susan Wnuk, Ph.D
Research Sponsored by University Health Network, Toronto
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change from baseline to 8 weeks, 6 months, and 12 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing whether a mindfulness-based training program can help people who have had bariatric surgery to better manage their weight and improve their mental and physical health.
Who is the study for?
This trial is for English-speaking adults who had bariatric surgery at least six months ago, are struggling to follow post-surgery eating guidelines, and can attend group sessions. It's not for those with severe depression or anxiety, active suicidal thoughts, serious mental illness like psychosis or bipolar disorder, or current PTSD symptoms.
What is being tested?
The study tests if Mindfulness Based Eating Awareness Training (MB-EAT) helps maintain weight loss and improves mental and physical health in post-bariatric surgery patients compared to those who don't receive this training.
What are the potential side effects?
Since the intervention involves mindfulness training rather than medication, typical drug side effects aren't expected. However, participants may experience emotional discomfort when discussing eating habits or confronting personal issues during sessions.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change from baseline to 8 weeks, 6 months, and 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from baseline to 8 weeks, 6 months, and 12 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Body Mass Index (BMI)
Change in weight
Height
Secondary study objectives
Body Parts Satisfaction Scale (BPSS)
Body Satisfaction Questionnaire (BSQ)
Difficulties in Emotion Regulation Scale (DERS)
+8 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: MB-EATExperimental Treatment1 Intervention
Behavioral: group psychotherapy. Eight weekly sessions, each session is 2 hours in duration.
Group II: Waitlist ControlActive Control1 Intervention
Wait list control.
Find a Location
Who is running the clinical trial?
University Health Network, TorontoLead Sponsor
1,523 Previous Clinical Trials
503,113 Total Patients Enrolled
13 Trials studying Obesity
893 Patients Enrolled for Obesity
Susan Wnuk, Ph.DPrincipal InvestigatorUniversity Health Network, Toronto
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: MB-EAT
- Group 2: Waitlist Control
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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