Binge Eating and Chromium Study (BEACh)
Primary Purpose
Binge Eating Disorder
Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Sugar Pill
chromium picolinate
chromium picolinate
Sponsored by
About this trial
This is an interventional treatment trial for Binge Eating Disorder focused on measuring binge eating, chromium, mood, glucose, appetite
Eligibility Criteria
Inclusion Criteria:
- Currently meets DSM-IV criteria for binge eating disorder (BED);
- Is able to provide informed consent and meet study visit requirements; and
- Is psychiatrically stable (e.g., no current suicidal or homicidal intent or other psychiatric condition that requires acute intervention).
Exclusion Criteria:
- Body mass index (BMI) < 24.9 kg/m^2 (underweight or normal weight) or ≥ 40 kg/m^2 (severely obese);
- Postmenopausal;
- Age < 18 or > 55 years;
- Pregnant, planning on becoming pregnant during the study period, or lactating;
- Current psychotropic medication use;
- Current use of insulin or other medications to control glucose metabolism;
- Current use of medications known to significantly influence appetite or weight [i.e., over-the-counter appetite suppressants that contain phentermine or sibutramine, atypical antipsychotic agents with high weight gain liability (such as olanzapine, risperidone, etc), prednisone, etc.];
- Fasting glucose level > 126 mg/dL (indicative of diabetes); and
- Creatinine level indicating renal insufficiency (> 1.0 for women; > 1.2 for men).
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Placebo Comparator
Active Comparator
Active Comparator
Arm Label
Sugar pill
low dose
high dose chromium picolinate
Arm Description
6 months treatment with placebo
600ug/day chromium picolinate for 6 months
1000 ug/day
Outcomes
Primary Outcome Measures
binge eating frequency
Secondary Outcome Measures
mood
insulin sensitivity
body weight
Full Information
NCT ID
NCT00904306
First Posted
May 17, 2009
Last Updated
April 2, 2012
Sponsor
University of North Carolina, Chapel Hill
Collaborators
National Alliance for Research on Schizophrenia and Depression
1. Study Identification
Unique Protocol Identification Number
NCT00904306
Brief Title
Binge Eating and Chromium Study
Acronym
BEACh
Official Title
Chromium Picolinate in Binge Eating Disorder: A Feasibility Study
Study Type
Interventional
2. Study Status
Record Verification Date
April 2012
Overall Recruitment Status
Completed
Study Start Date
July 2008 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
July 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of North Carolina, Chapel Hill
Collaborators
National Alliance for Research on Schizophrenia and Depression
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to test the feasibility and preliminary efficacy of a 6-month chromium picolinate (CrPic) treatment trial in binge eating disorder (BED).
Detailed Description
Binge eating (i.e., the consumption of unusually large amounts of food with a sense of loss of control) is a common problem with serious public health implications in large part due to its role in obesity. Binge eating leads to weight gain and is common in overweight individuals. Current treatments for binge eating disorder (BED) are inadequate, and previous randomized treatment trials have suffered from high drop out rate due to the adverse effects of pharmacological agents. Chromium picolinate is a dietary supplement that has been shown to reduce symptoms of depression and appetite regulation problems in patients with atypical depression; chromium picolinate also affects insulin regulation and has been shown to improve glucose levels in patients with type-2 diabetes. This pilot study will evaluate the effect of chromium picolinate on binge eating, mood, body weight, and glucose regulation in overweight individuals with BED.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Binge Eating Disorder
Keywords
binge eating, chromium, mood, glucose, appetite
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
26 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sugar pill
Arm Type
Placebo Comparator
Arm Description
6 months treatment with placebo
Arm Title
low dose
Arm Type
Active Comparator
Arm Description
600ug/day chromium picolinate for 6 months
Arm Title
high dose chromium picolinate
Arm Type
Active Comparator
Arm Description
1000 ug/day
Intervention Type
Dietary Supplement
Intervention Name(s)
Sugar Pill
Intervention Description
placebo oral tablet taken once per day
Intervention Type
Dietary Supplement
Intervention Name(s)
chromium picolinate
Intervention Description
1000 ug/day chromium picolinate for 6 months
Intervention Type
Dietary Supplement
Intervention Name(s)
chromium picolinate
Intervention Description
600 ug/day chromium picolinate
Primary Outcome Measure Information:
Title
binge eating frequency
Time Frame
baseline, 3 and 6 months, 3-month followup
Secondary Outcome Measure Information:
Title
mood
Time Frame
baseline, 3 adn 6 months, 3-month followup
Title
insulin sensitivity
Time Frame
baseline, 3 adn 6 months, 3-month followup
Title
body weight
Time Frame
baseline, 3 adn 6 months, 3-month followup
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Currently meets DSM-IV criteria for binge eating disorder (BED);
Is able to provide informed consent and meet study visit requirements; and
Is psychiatrically stable (e.g., no current suicidal or homicidal intent or other psychiatric condition that requires acute intervention).
Exclusion Criteria:
Body mass index (BMI) < 24.9 kg/m^2 (underweight or normal weight) or ≥ 40 kg/m^2 (severely obese);
Postmenopausal;
Age < 18 or > 55 years;
Pregnant, planning on becoming pregnant during the study period, or lactating;
Current psychotropic medication use;
Current use of insulin or other medications to control glucose metabolism;
Current use of medications known to significantly influence appetite or weight [i.e., over-the-counter appetite suppressants that contain phentermine or sibutramine, atypical antipsychotic agents with high weight gain liability (such as olanzapine, risperidone, etc), prednisone, etc.];
Fasting glucose level > 126 mg/dL (indicative of diabetes); and
Creatinine level indicating renal insufficiency (> 1.0 for women; > 1.2 for men).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kimberly A Brownley, PhD
Organizational Affiliation
University of North Carolina, Chapel Hill
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
17370289
Citation
Brownley KA, Berkman ND, Sedway JA, Lohr KN, Bulik CM. Binge eating disorder treatment: a systematic review of randomized controlled trials. Int J Eat Disord. 2007 May;40(4):337-48. doi: 10.1002/eat.20370.
Results Reference
background
PubMed Identifier
18188431
Citation
Bulik CM, Brownley KA, Shapiro JR. Diagnosis and management of binge eating disorder. World Psychiatry. 2007 Oct;6(3):142-8.
Results Reference
background
PubMed Identifier
17628126
Citation
Berkman ND, Bulik CM, Brownley KA, Lohr KN, Sedway JA, Rooks A, Gartlehner G. Management of eating disorders. Evid Rep Technol Assess (Full Rep). 2006 Apr;(135):1-166.
Results Reference
background
PubMed Identifier
23751236
Citation
Brownley KA, Von Holle A, Hamer RM, La Via M, Bulik CM. A double-blind, randomized pilot trial of chromium picolinate for binge eating disorder: results of the Binge Eating and Chromium (BEACh) study. J Psychosom Res. 2013 Jul;75(1):36-42. doi: 10.1016/j.jpsychores.2013.03.092. Epub 2013 Apr 22.
Results Reference
derived
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Binge Eating and Chromium Study
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