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

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.

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

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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