Effect of Exercise on Chocolate Addiction

NCT ID: NCT03356509

Last Updated: 2018-09-18

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

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-01-08

Study Completion Date

2018-09-15

Brief Summary

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The study will use stress inducing tasks to determine if there are significant improvements in mood, chocolate cravings, and attentional bias to chocolate in overweight/obese chocolate abusers following rest and a bout of high intensity interval exercise.

Detailed Description

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The purpose of this research study is to investigate whether a single high intensity interval exercise (HIIE) bout, following two stress-inducing tasks, reduces addictive behavior to chocolate. Volunteers must complete the consent form before being able to participate in two days of testing (exercise day and control day) which will be presented in randomized order. The two days will be separated by a one to 7 day washout period. Subjects will be required to submit a three day chocolate diary then abstain from chocolate on the 4th day. They will also be asked to record everything they eat and drink on the day before and the morning of the study and list three types of chocolate they crave most. Two stress-inducing tasks will be performed on both days followed by completion of either 26 minutes of HIIE or seated resting condition followed by the completion of two mood and craving questionnaires. They will finally be asked to complete a task that measures the amount of attention they pay to chocolate. Statistical analyses will be conducted to determine the effect of either exercising or not on addictive behaviors to chocolate.

Conditions

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Acute Exercise and Addictive Behavior

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Exercise

They will do a 26-min bout of high intensity interval exercise.

Group Type EXPERIMENTAL

Exercise

Intervention Type BEHAVIORAL

Exercise will be performed on a stationary bicycle ergometer.

No exercise

They will sit quietly for 26 minutes without access to electronic devices or reading materials.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Exercise

Exercise will be performed on a stationary bicycle ergometer.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* BMI equal or greater than 25
* Eat at least 3.5 oz of chocolate per day
* Scorer at least 33 out of a possible 36 on the Handedness Questionnaire
* Ability to provide informed consent
* No medical contraindications to exercise
* Premenopausal

Exclusion Criteria

* PMS
* Pregnancy
* Prisoners
* Risk factors for heart disease as determined by physician
* Medication that interferes with capacity to exercise
* Answer "Yes" to PAR-Q
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Miami

OTHER

Sponsor Role lead

Responsible Party

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Arlette Perry

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Laboratory of Clinical and Applied Physiology

Coral Gables, Florida, United States

Site Status

Countries

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United States

Other Identifiers

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20170895

Identifier Type: -

Identifier Source: org_study_id

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