Crave Crush Neuroimaging Study

NCT ID: NCT02949102

Last Updated: 2018-07-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-12-31

Study Completion Date

2016-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of the research is to test whether a gymnemic acids (GA) lozenge will reduce reward region response to intake of high-sugar food and ad lib candy intake and whether the GA lozenge reduced reward region response to anticipated intake of high-sugar food and high-sugar food pictures relative to a placebo lozenge.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Test the hypothesis that an acute dose of Crave Crush will produce greater reductions in reward region response to a taste of a high-sugar/high-fat beverage and anticipated receipt of this beverage than a placebo dose.

Test the hypothesis that a dose of Crave Crush will result in reduced ad lib candy intake while the participants complete a survey after the fMRI scan. Participants will receive a second dose of Crave Crush or placebo. They will then be placed in a room to complete a few surveys. A bowl of candy will be placed on the table. Participants will be told that the candy is left over from their assessment and that they are free to have as much as they like, because the candy must be discarded after each participant.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Obesity

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Crave Crush

Crave Crush is a plant-based tablet that alters taste perception by affecting sweet taste receptors on the tongue.

Group Type EXPERIMENTAL

Crave Crush

Intervention Type DIETARY_SUPPLEMENT

Crave Crush is a dietary supplement that affects sweet taste receptors on the tongue.

Placebo

The placebo tablet is comparable in taste and is comprised primarily of sorbitol.

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DIETARY_SUPPLEMENT

The placebo tablet is comparable in taste and is comprised primarily of sorbitol.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Crave Crush

Crave Crush is a dietary supplement that affects sweet taste receptors on the tongue.

Intervention Type DIETARY_SUPPLEMENT

Placebo

The placebo tablet is comparable in taste and is comprised primarily of sorbitol.

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Between 18 and 50 years old
* report having a sweet tooth
* report desire to lose weight
* Body Mass Index between 18 and 40

Exclusion Criteria

* major psychiatric disorders
* serious health problems (e.g., diabetes)
* habitual use of psychoactive drugs or medications
* contraindications for MRI scanning (e.g., ferromagnetic braces)
* gluten or lactose intolerance
* a vegan diet.
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Cravecrush

UNKNOWN

Sponsor Role collaborator

Oregon Behavioral Intervention Strategies, Inc.

INDUSTRY

Sponsor Role collaborator

Oregon Research Behavioral Intervention Strategies, Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Eric Stice, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Oregon Research Behavioral Intervention Strategies

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

FOUR002

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Binge Eating and Chromium Study
NCT00904306 COMPLETED PHASE1/PHASE2
tDCS and Emotional Eating
NCT06488287 RECRUITING NA