AzTrials
AzTrials

Obesity PreventionVeTNCT01196351

Activity at Ventilation Threshold on Appetite and Food Intake in Boys

A study testing Dietary Supplement: water with noncalorie sweetener and Activity: With noncalorie sweetener or glucose in people with Obesity Prevention, run by University of Toronto at 1 site in Canada.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The investigators hypothesize exercise increases short term appetite and food intake, and interferes with satiety and satiations to a preload in normal weight, overweight and obese boys. Read more about this study

Who is it for?
Ages 9 to 14 years, men onlyHealthy volunteers can take part
Conditions the study is for
Obesity Prevention
What is being tested?
Dietary Supplement: water with noncalorie sweetener and Activity: With noncalorie sweetener or glucose
Could I receive a placebo?
No, everyone receives an active treatment
How many people
35 participants
Where
1 siteCanada
Study dates
Oct 2008to Sep 2009
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 9 to 14 years
  • Men only
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • Healthy boys with no emotional, behavioral or learning problems

Who cannot join

  • Girls

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • Department of Nutritional Sciences

    Toronto, Ontario, M5S 3E2

Other trials in Canada

About this study

Official title: Effect of Activity at the Ventilation Threshold on Appetite and Food Intake After a Glucose Drink in Normal Weight, Overweight and Obese Boys

The investigators hypothesize exercise increases short term appetite and food intake, and interferes with satiety and satiations to a preload in normal weight, overweight and obese boys.

Read the detailed description

The effect of exercise (EXR) on short-term food intake (FI) and subjective appetite was investigated in normal weight (NW), overweight (OW) and obese (OB) boys were randomized into 4 treatments. Each boy consumed either a non-caloric sweetened control (CON) or GLU drink after either exercise (EXR) or sedentary activity. Subjects exercised at their ventilation threshold (VeT).

Being tested
Dietary Supplement: water with noncalorie sweetener, Activity: With noncalorie sweetener or glucose
Keywords
boys, obesity, physical activity, exercise
Medical subject headings
Obesity, Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Dietary Supplement: water with noncalorie sweetenerOther

  • Activity: With noncalorie sweetener or glucoseOther

Study groups in NCT01196351
Study groupRoleWhat they receive
Sedentary activity, noncaloric beverageExperimentalNot described
Receives: Other: Dietary Supplement: water with noncalorie sweetener
Sedentary activity, glucose beverageExperimentalNot described
Receives: Other: Dietary Supplement: water with noncalorie sweetener
Exercise activity, noncaloric beverageExperimentalNot described
Receives: Other: Activity: With noncalorie sweetener or glucose
Exercise activity, glucose beverageExperimentalNot described
Receives: Other: Activity: With noncalorie sweetener or glucose

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. food intake (kcal)

    Measured: at 30-35 min after the treatment

Secondary outcomes (1)
  1. Subjective appetite

    Measured: 0-80 min

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Sep 2010 (estimated)
  2. Study startOct 2008
  3. Primary completionSep 2009
  4. Study completionSep 2009

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Crossover
Masking
Single blind
Who is masked
Participant
Enrolment
35 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01196351
Sponsor's protocol ID
CIHR-Kids21595_EXR1
Other IDs
CIHR
Acronym
VeT
Status last verified
Sep 2010
First submitted
3 Sep 2010
Last updated
8 Sep 2010
Results posted
No
Data monitoring committee
No

Publications

  • Bellissimo N, Desantadina MV, Pencharz PB, Berall GB, Thomas SG, Anderson GH. A comparison of short-term appetite and energy intakes in normal weight and obese boys following glucose and whey-protein drinks. Int J Obes (Lond). 2008 Feb;32(2):362-71. doi: 10.1038/sj.ijo.0803709. Epub 2007 Aug 14.

    PubMed 17700578
  • Bellissimo N, Thomas SG, Goode RC, Anderson GH. Effect of short-duration physical activity and ventilation threshold on subjective appetite and short-term energy intake in boys. Appetite. 2007 Nov;49(3):644-51. doi: 10.1016/j.appet.2007.04.004. Epub 2007 Apr 22.

    PubMed 17537539
  • Bozinovski NC, Bellissimo N, Thomas SG, Pencharz PB, Goode RC, Anderson GH. The effect of duration of exercise at the ventilation threshold on subjective appetite and short-term food intake in 9 to 14 year old boys and girls. Int J Behav Nutr Phys Act. 2009 Oct 9;6:66. doi: 10.1186/1479-5868-6-66.

    PubMed 19818131

Questions about this trial

What is this clinical trial studying?

A study testing Dietary Supplement: water with noncalorie sweetener and Activity: With noncalorie sweetener or glucose in people with Obesity Prevention, run by University of Toronto at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 8 Sep 2010. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

food intake (kcal) (time frame: at 30-35 min after the treatment). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01196351, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Sep 2010.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in