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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01926431
Other study ID # fMRI Study
Secondary ID ERN_09-586
Status Completed
Phase N/A
First received August 20, 2013
Last updated August 20, 2013
Start date September 2009
Est. completion date May 2011

Study information

Verified date August 2013
Source University of Birmingham
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Interventional

Clinical Trial Summary

The primary aim of this study was to determine the effects of an acute bout of high intensity exercise on the brains response to viewing pictures of food using functional magnetic resonance imaging (fMRI).


Description:

It is clear that intense exercise impacts on peripheral appetite regulation, however very little is known about the impact of high-intensity exercise on central appetite regulation. This study aimed to investigate the effects of high-intensity exercise on both central and peripheral responses to images of food. Functional magnetic resonance techniques were used to assess the brains response to images of high and low calorie foods, following a short bout of high-intensity exercise. Appetite hormone concentrations were also measured. It was hypothesized that, due to the known effects of high-intensity exercise on appetite regulatory hormones and subjective appetite ratings, the activation of reward-related brain regions to visual food cues would be modulated following intense physical activity.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date May 2011
Est. primary completion date May 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- Healthy, non-smokers, free from cardiovascular disease and metabolic disease, no medication, participated in moderate/vigorous physical activity (>2 hours per week)

Exclusion Criteria:

- Smokers, history of cardiovascular/metabolic disease, low physical activity levels, inability to participate in fMRI scanning sessions including contraindications to MRI

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Basic Science


Intervention

Other:
Exercise

Rest


Locations

Country Name City State
United Kingdom Birmingham University Imaging Centre Birmingham Midlands

Sponsors (1)

Lead Sponsor Collaborator
University of Birmingham

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Neural responses following exercise and rest Volunteers completed an fMRI assessment following 60 minutes of intense exercise and 60 minutes of rest on two separate occasions. Ten minutes post-exercise/rest No
Secondary Appetite hormones Blood samples were taken using a cannula system for both trials. Concentrations of appetite regulating hormones were measured from plasma. Blood samples taken at baseline, following exercise/rest, prior to the fMRI assessment and immediately following the fMRI assessment No
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