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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00912210
Other study ID # UIUC IRB 07782
Secondary ID
Status Completed
Phase Phase 1
First received May 29, 2009
Last updated May 29, 2009
Start date April 2009

Study information

Verified date May 2009
Source University of Illinois at Urbana-Champaign
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The broad aim is to determine efficacy of a weight loss diet higher in protein and lower in carbohydrate combined with low intensity exercise to favorably impact body composition, bone health, physical function, metabolic disease and quality of life compared to a conventional higher carbohydrate diet in overweight women over age 60.


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 60 Years to 80 Years
Eligibility Inclusion Criteria:

- Body mass index > 28 kg/m²

- Clearance of primary physician to participate in diet and mild exercise

Exclusion Criteria:

- Medical condition contraindicating prescribed diet and exercise regimen

- Type 2 Diabetes Mellitus

- Physically active lifestyle (>30 min moderate physical activity 2+ times weekly)

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Basic Science


Intervention

Dietary Supplement:
Whey protein isolate
Loss of 10% baseline weight over 6 months, with whey protein isolate supplemented at 50g/day (two 25 g doses taken at breakfast and afternoon snack mixed with food or beverage)
Maltodextrin powder supplement
Loss of 10% baseline weight over 6 months, with whey protein isolate supplemented at 50 g / day (two 25 g doses at breakfast and afternoon snack mixed with food or beverage)

Locations

Country Name City State
United States University of Illinois at Urbana-Champaign Urbana Illinois

Sponsors (1)

Lead Sponsor Collaborator
University of Illinois at Urbana-Champaign

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bone and body composition: Weight, percent fat, muscle and fat distribution in the thigh and abdomen and bone density and structural quality assessed by DXA and structural MRI Baseline and post 6 months weight loss No
Secondary Physical function: balance, gait, strength and activities of daily living Baseline and post 6 months weight loss No
Secondary Quality of life Baseline and post 6 months weight loss No
Secondary Metabolic syndrome: insulin resistance, blood pressure, blood lipids, waist circumference Baseline and post 6 months weight loss No
Secondary Acid-base balance Baseline and post 1 and 6 months weight loss No
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