- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02190136
Yoga Improves Aerobic Fitness, Glycemia and Mood State and Reduces Abdominal Obesity (PRISE)
July 11, 2014 updated by: Paul Arciero, Skidmore College
Yoga Improves Aerobic Fitness, Glycemia and Mood State and Reduces Abdominal Obesity in Overweight Women: The PRISE Study
Stretching and flexibility exercise such as yoga and functional resistance exercise are two forms of exercise that are growing in popularity.
However, they have not been scientifically tested to demonstrate their ability to improve body composition, fitness, heart and metabolic health, and mood state in overweight/obese women.
The investigators hypothesize that during an 11 week intervention, both forms of exercise will improve body composition, heart and metabolic health and mood state.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study was a 11 week protein-rich whole food diet and exercise training intervention in middle aged overweight/obese women.
Subjects were randomized into 3 groups: Protein-rich whole food only consumed as 20-25 grams per serving 4-6 per day (P); protein and resistance exercise training (R); and protein and stretching/yoga exercise training (S).
All outcomes, including the primary outcomes of body composition and cardiometabolic biomarkers were measured at baseline (week 0) and post-intervention (week 12) in all study subjects.
Study Type
Interventional
Enrollment (Actual)
39
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
Saratoga Springs, New York, United States, 12866
- Human Nutrition and Metabolism Laboratory
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
25 years to 60 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- obese or overweight women
- between ages 25-60 and
- otherwise healthy
Exclusion Criteria:
- smokers,
- habitual exercisers
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Protein whole foods
Ingestion of 20-25 grams per serving consumed 4-6 times per day; 1 within an hour of waking in the morning and the other 2.5-3 hours apart during the day.
|
Protein-rich whole foods consumed at 20-30 grams of protein at each of 4-6 meals per day
Protein rich whole foods diet and resistance training 3 times per week for 11 weeks
Protein-rich whole foods diet of 20-30 grams of protein at each of 4-6 meals per day with stretching/yoga training 3 times per week for 11 weeks
|
Experimental: Protein Resistance Exercise Training
Ingestion of 4-6 protein-rich meals per day and 3 times per week of resistance functional training.
|
Protein-rich whole foods consumed at 20-30 grams of protein at each of 4-6 meals per day
Protein rich whole foods diet and resistance training 3 times per week for 11 weeks
|
Experimental: Protein Stretching/Yoga Training
Ingestion of Protein-rich diet 4-6 meals/day and stretching/yoga training 3 times per week
|
Protein-rich whole foods consumed at 20-30 grams of protein at each of 4-6 meals per day
Protein-rich whole foods diet of 20-30 grams of protein at each of 4-6 meals per day with stretching/yoga training 3 times per week for 11 weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Total and Regional Body Composition
Time Frame: baseline and 11 weeks
|
Total and regional body composition was assessed by dual energy xray absorptiometry (DXA) at baseline and 11 weeks in all subjects
|
baseline and 11 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Aerobic Fitness
Time Frame: baseline and 11 weeks
|
VO2 max was assessed in each subject at baseline and 11 weeks
|
baseline and 11 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Plasma Biomarkers
Time Frame: baseline and 11 weeks
|
Insulin, glucose, and leptin was assessed in each subject at baseline and 11 weeks
|
baseline and 11 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2006
Primary Completion (Actual)
January 1, 2008
Study Completion (Actual)
July 1, 2014
Study Registration Dates
First Submitted
July 7, 2014
First Submitted That Met QC Criteria
July 11, 2014
First Posted (Estimate)
July 15, 2014
Study Record Updates
Last Update Posted (Estimate)
July 15, 2014
Last Update Submitted That Met QC Criteria
July 11, 2014
Last Verified
July 1, 2014
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Yoga-0610-52
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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