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Mindful Motivation for Binge Eating

N/A
Waitlist Available
Led By Rachel Radin, PhD
Research Sponsored by University of California, San Francisco
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Aged 18 years or older
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline to post-intervention, an anticipated average of 8 weeks
Awards & highlights
No Placebo-Only Group

Summary

"This trial aims to test a new eating intervention for overweight individuals with binge eating. The intervention combines mindful eating with motivational interviewing to target binge eating. Researchers want to find out if participants find the intervention acceptable

Who is the study for?
This trial is for individuals who are overweight and struggle with binge eating. Participants will be asked to complete online questionnaires, provide body composition data, and meditate daily. They must not have conditions that exclude them from the study.
What is being tested?
The trial tests a new intervention combining mindful eating techniques with motivational interviewing against an active control of digital meditation alone. The goal is to see if this approach can reduce binge eating episodes.
What are the potential side effects?
Since the interventions involve behavioral strategies like meditation and counseling, side effects may include increased self-awareness or emotional discomfort but typically do not involve physical side effects.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am 18 years old or older.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to post-intervention, an anticipated average of 8 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline to post-intervention, an anticipated average of 8 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in Client Satisfaction score, as determined by the total score on the Client Satisfaction Questionnaire (CSQ-8)
Change in Credibility/Expectancy and Satisfaction Questionnaire (CEQ) score, as determined by total score on the CEQ
Percentage of participants attending a booster call # 1
+4 more
Secondary study objectives
Change in Questionnaire on Eating and Weight Patterns (QEWP) frequency of binge eating episodes per month
Change in Reward Based Eating Drive Scale (RED-13) score, as determined by total score on the RED-13.
Change in Weight Efficacy Lifestyle Scale (WEL-SF) score, as determined by total score on the WEL-SF
+2 more

Awards & 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: Mindful Motivation GroupExperimental Treatment2 Interventions
Participants will be assigned to a eating intervention that combines general mindfulness (via headspace) with motivational interviewing for mindful eating They will be asked to attend an online counseling session along with three 10-minute booster phone calls. They will be asked to engage with a digital-based mindful eating program once per week over the course of 8 weeks. In addition, participants will have access to optional educational materials on mindful eating and an optional online private support forum after the intervention period is finished.
Group II: Active Control ConditionActive Control1 Intervention
Participants in the meditation intervention group will be assigned to a digitally-based meditation intervention (via Headspace) and asked to use this for at least 10 minutes a day over the course of 8 weeks.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Meditation
2021
Completed Phase 3
~2940

Find a Location

Who is running the clinical trial?

University of California, San FranciscoLead Sponsor
2,591 Previous Clinical Trials
14,901,503 Total Patients Enrolled
35 Trials studying Obesity
11,445 Patients Enrolled for Obesity
DexCom, Inc.Industry Sponsor
145 Previous Clinical Trials
35,391 Total Patients Enrolled
1 Trials studying Obesity
23 Patients Enrolled for Obesity
National Center for Complementary and Integrative Health (NCCIH)NIH
862 Previous Clinical Trials
674,001 Total Patients Enrolled
32 Trials studying Obesity
4,260 Patients Enrolled for Obesity
Headspace Meditation LimitedIndustry Sponsor
5 Previous Clinical Trials
1,528 Total Patients Enrolled
Rachel Radin, PhDPrincipal InvestigatorUniversity of California, San Francisco
1 Previous Clinical Trials
163 Total Patients Enrolled
Elissa Epel, PhDPrincipal InvestigatorUniversity of California, San Francisco
13 Previous Clinical Trials
2,745 Total Patients Enrolled
4 Trials studying Obesity
464 Patients Enrolled for Obesity
~67 spots leftby Aug 2026