Enhancing Fitness in Older Pre-diabetic Veterans

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Department of Veterans Affairs
ClinicalTrials.gov Identifier:
NCT00594399
First received: January 3, 2008
Last updated: April 6, 2015
Last verified: August 2014
  Purpose

This study targets older adults (ages 60 and over) who are overweight (body mass index 25-40) with impaired fasting glucose (100 - 125). We propose a three-year, randomized controlled clinical trial (n=300) to determine the effect of a one-year physical activity counseling intervention on glucose metabolism and secondary outcomes compared to usual care.


Condition Intervention Phase
Impaired Glucose Tolerance
Obesity
Diabetes
Behavioral: Physical Activity Counseling
Phase 2
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Prevention
Official Title: Enhancing Fitness in Older Overweight Vets With Impaired Fasting Glucose

Resource links provided by NLM:


Further study details as provided by Department of Veterans Affairs:

Primary Outcome Measures:
  • Fasting Insulin [ Time Frame: Baseline ] [ Designated as safety issue: No ]
    Fasting Insulin analyzed at VA central laboratory by technicians not affiliated with study. Participants were instructed to refrain from eating or drinking anything except water and medications past midnight. A reminder call was placed the night before the scheduled appointment and fasting was verified by study personnel before appointed blood draws.

  • 3 Month Fasting Insulin [ Time Frame: 3 month ] [ Designated as safety issue: No ]
  • 12 Month Fasting Insulin [ Time Frame: 12 months ] [ Designated as safety issue: No ]
  • Fasting Glucose [ Time Frame: Baseline ] [ Designated as safety issue: No ]
  • 3 Month Fasting Glucose [ Time Frame: 3 months ] [ Designated as safety issue: No ]
  • 12 Month Fasting Glucose [ Time Frame: 12 Months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Physical Activity, Endurance [ Time Frame: Baseline ] [ Designated as safety issue: No ]
    Physical activity, endurance/aerobic activities by self-report from the CHAMPS questionnaire of physical activity for older adults.

  • Physical Activity, Endurance [ Time Frame: 3 months ] [ Designated as safety issue: No ]
    Physical activity, endurance/aerobic activities by self-report from the CHAMPS questionnaire of physical activity for older adults.

  • Physical Activity, Endurance [ Time Frame: 12 Months ] [ Designated as safety issue: No ]
    Physical activity, endurance/aerobic activities by self-report from the CHAMPS questionnaire of physical activity for older adults.


Enrollment: 302
Study Start Date: October 2008
Study Completion Date: June 2011
Primary Completion Date: March 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Arm 1 Physical Activity counseling
Physical activity (PA) counseling program with the following components: baseline in-person counseling session; telephone calls, one physician endorsement of PA in a primary care clinic visit, monthly automated telephone calls from the primary care provider encouraging PA; and quarterly mailed materials providing personalized feedback.
Behavioral: Physical Activity Counseling
Physical activity (PA) counseling program with the following components: a baseline in-person counseling session; telephone calls biweekly for 6 weeks then monthly; one physician endorsement of PA in a primary care clinic visit; monthly automated telephone calls from the primary care provider encouraging PA; and (5) quarterly mailed materials providing personalized feedback.
No Intervention: Arm 2
Usual care from primary, womens or geriatric clinics

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   60 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • VA patients followed by the Durham VA Primary Care, Women's Health, and Geriatric clinics
  • Must have had more than one visit to the VA in preceding 12 months
  • Age 60 and over
  • Impaired glucose intolerance documented by recent fasting blood glucose between 100 and 125 mg/dL
  • Body mass index between 25-40 kg/m2
  • Able to walk 10 meters without human assistance (assistive device acceptable)
  • All participants must be assigned a primary care provider and have had more than one visit to the VA in the preceding 12 months

Exclusion Criteria:

  • Free of frank diabetes
  • Fasting blood sugar above 125 mg/dL
  • HbA1c > 7%
  • Unstable angina
  • Recent history of ventricular tachycardia
  • Unstable chronic obstructive pulmonary disease (two hospitalizations within the previous 12 months and/or on oxygen)
  • Uncontrolled hypertension (diastolic blood pressure >110 mm/Hg or systolic > 200mm/Hg)
  • Stroke with moderate to severe aphasia
  • Diagnosis of chronic pain which may interfere with their ability to be physically active
  • Diagnosis of unstable mental or behavioral disorder
  • Diagnosis of memory loss or dementia
  • Visual or hearing loss severe enough to interfere with ability to receive telephone counseling and review written materials
  • Active substance abuse
  • A terminal diagnosis
  • Followed by VA for medications only
  • Regularly, vigorously physically active for six months or longer.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00594399

Locations
United States, North Carolina
Durham VA Medical Center, Durham, NC
Durham, North Carolina, United States, 27705
Sponsors and Collaborators
Investigators
Principal Investigator: Miriam C. Morey, PhD Durham VA Medical Center, Durham, NC
  More Information

Publications:

Responsible Party: Department of Veterans Affairs
ClinicalTrials.gov Identifier: NCT00594399     History of Changes
Other Study ID Numbers: IIR 06-252
Study First Received: January 3, 2008
Results First Received: October 1, 2014
Last Updated: April 6, 2015
Health Authority: United States: Federal Government

Keywords provided by Department of Veterans Affairs:
Aging
Exercise
Impaired Glucose Tolerance
Obesity
Functional Status
Disability
Health Services Research
Randomized Controlled Trial
Diabetes
Adaptive Randomization Design

Additional relevant MeSH terms:
Glucose Intolerance
Glucose Metabolism Disorders
Hyperglycemia
Metabolic Diseases

ClinicalTrials.gov processed this record on August 31, 2015