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Specific Time Exercise for Obesity

N/A

Recruiting

Research Sponsored by Université de Montréal

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be younger than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up within the 30 minutes devoted to chemosensory testing, prior to the meal at noon, and in the 2 hour period following meal.

Awards & highlights

Study Summary

This trial will assess the impact of the timing of exercise on sensory perception and energy intake in teenagers.

Who is the study for?

This trial is for boys and girls aged 12-17 with normal weight or obesity. They must attend high school, not follow a specific diet, have no food allergies, eating disorders, intestinal or metabolic diseases. They can't take certain medications like insulin or be physically unable to exercise. Participants must speak French or English and not be competitive athletes, vegetarians/vegans, smokers, or drug users.Check my eligibility

What is being tested?

The study tests how exercising at different times affects teenagers' sense of taste and smell and their appetite after working out. It aims to find the best time for exercise to reduce hunger post-workout. The research includes treadmill exercises at two morning times versus a sedentary condition across three visits.See study design

What are the potential side effects?

Since this trial involves moderate to vigorous physical activity on a treadmill, potential side effects may include typical exercise-related issues such as muscle soreness, fatigue, shortness of breath during exertion, and possibly mild injuries.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ within the 30 minutes devoted to chemosensory testing, prior to the meal at noon, and in the 2 hour period following meal.

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~within the 30 minutes devoted to chemosensory testing, prior to the meal at noon, and in the 2 hour period following meal.

This trial's timeline: 3 weeks for screening, Varies for treatment, and within the 30 minutes devoted to chemosensory testing, prior to the meal at noon, and in the 2 hour period following meal. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Eating habits outside the laboratory

Energy intake at lunch

Physical activity habits outside the laboratory

+2 more

Secondary outcome measures

Chemosensory response - Smell

Chemosensory response - Taste

Circulating concentration of GLP1

+3 more

Trial Design

3Treatment groups

Experimental Treatment

Active Control

Group I: EX starts at 9:30 amExperimental Treatment1 Intervention

A warm-up, 30 min at 70% VO2 max and a cool-down performed at 9:30 am.

Group II: EX starts at 11:00 amExperimental Treatment1 Intervention

A warm-up, 30 min at 70% VO2 max and a cool-down performed at 11:00 am.

Group III: No EXActive Control1 Intervention

Control condition. A choice of 30 minutes sedentary activities.

Do I qualify?Apply below to find out

Find a Location

Who is running the clinical trial?

Université de MontréalLead Sponsor

215 Previous Clinical Trials

102,775 Total Patients Enrolled

Canadian Institutes of Health Research (CIHR)OTHER_GOV

1,348 Previous Clinical Trials

26,455,672 Total Patients Enrolled

Media Library

Acute moderate to vigorous exercise performed at a specific moment of the day Clinical Trial Eligibility Overview. Trial Name: NCT05030636 — N/A

Exercise Timing in Obesity Research Study Groups: EX starts at 9:30 am, No EX, EX starts at 11:00 am

Exercise Timing in Obesity Clinical Trial 2023: Acute moderate to vigorous exercise performed at a specific moment of the day Highlights & Side Effects. Trial Name: NCT05030636 — N/A

Acute moderate to vigorous exercise performed at a specific moment of the day 2023 Treatment Timeline for Medical Study. Trial Name: NCT05030636 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there any open enrollment opportunities for this research study?

"Affirmative. Information accessible on clinicaltrials.gov reveals that this medical research, first advertised on September 15th 2021 is still open for recruitment. In total 36 patients are needed to be enrolled at one single location."

Answered by AI

Are senior citizens being considered as prospective participants in this trial?

"This trial is available to those aged between 12 and 17. According to the eligibility criteria, there are 250 patient slots for minors and 604 open spots designated for elderly individuals."

Answered by AI

Can I join the proceedings of this medical research?

"This trial requires 36 volunteers between the ages of 12 and 17 that have been classified as obese by World Health Organisation standards. In addition to age, participants must be able to adhere to a regular school schedule in order for their data to remain reliable."

Answered by AI

What objectives is this trial seeking to accomplish?

"The primary endpoint of this 24-hour clinical trial is to analyse energy intake at lunch. Additionally, secondary endpoints include measuring circulating levels of ghrelin (anorexigenic hormonal levels), chemosensory response - smell (smell event-related potential using EEG) and the concentration of PYY (orexigenic hormones)."

Answered by AI

What is the current capacity for recruitment into this experiment?

"Affirmative. Clinicaltrials.gov records show that this study is actively recruiting participants, having been initially posted on September 15th 2021 and last updated August 31st 2021. 36 volunteers are needed to participate from a single location."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

Novel Role of Exercise Timing in Obesity

Marie-Ève Mathieu 2021. "Novel Role of Exercise Timing in Obesity". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT05030636.