Dose-Response to Exercise in Women Aged 45-75 Years (DREW)

Sponsor
Pennington Biomedical Research Center (Other)
Overall Status
Completed
CT.gov ID
NCT00011193
Collaborator
National Heart, Lung, and Blood Institute (NHLBI) (NIH)
464
2
71
232
3.3

Study Details

Study Description

Brief Summary

To investigate the effects of different amounts of exercise on both cardiorespiratory fitness and risk factors for cardiovascular disease in sedentary, overweight, mildly hypertensive, but healthy, postmenopausal women aged 45 to 75 years.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Exercise

Detailed Description

BACKGROUND:

The primary goal of the Dose-Response to Exercise in Women aged 45-75 Years (DREW) was to investigate the effects of different amounts of exercise on both cardiorespiratory fitness and risk factors for cardiovascular disease. Participants were sedentary, overweight or obese, postmenopausal women who had high normal blood pressure or Stage I hypertension, and thus are at moderately high risk for cardiovascular disease. A total of 464 women (about 35% were recruited from minority groups) were randomly assigned to a control group (N = 102) or to 1 of 3 exercise groups (N = 155 for the lowest exercise dose and 104 in the 8-kcal/kg group and 103 in the 12-kcal/kg exercise group). Women assigned to the exercise groups exercised for 6 months at energy expenditures of 4, 8, or 12 kcal ·kg-1 · week-1. These exercise doses represent the consensus public health recommendation for physical activity from recently published guidelines from the U.S. Public Health Service, American Heart Association, and American College of Sports Medicine (8 kcal ·kg-1 · week-1) and at doses 50% below (4 kcal ·kg-1 · week-1) and 50% above (12 kcal ·kg-1 · week-1) the consensus dose. All women exercised at 50% of V02 max. The exercise sessions took place in the exercise laboratory, with individual supervision of each session and strict control of frequency, duration, and intensity. This was provided thorough documentation of the exact amount of exercise completed. Primary outcome measures are VO2 max and resting systolic blood pressure. Other cardiovascular disease risk factors, psychosocial variables, health-related quality of life, body composition, and fat distribution are secondary outcomes. Other secondary analyses included a focus on the extent to which observed dose-response effects are modified by baseline levels of fitness, ethnicity, risk factors, or age. Assessments will take place at baseline and 6 months. The research provided information about (1) patterns of change in outcomes produced by each of several exercise doses, (2) whether performing exercise at less than the current consensus dose has any benefit, (3) whether performing more exercise than the consensus dose has greater (or proportionally greater) health benefits, and (4) the characteristics of sedentary women who are most likely to benefit from various exercise doses.

DESIGN NARRATIVE:

A total of 464 sedentary, postmenopausal women at moderate risk for cardiovascular disease was randomly assigned to receive exercise training at one of three doses (4, 8, or 12 kcal/kg/wk) or no exercise for six months duration. The specific aims were be to determine: (a) if women in the exercise groups have increased aerobic power (VO2max) over the six months compared to the no exercise group; (b) if women in the exercise groups have a greater reduction in resting systolic blood pressure than those in the no exercise group; and, (c) if there will be a dose-response gradient across the three exercise groups for changes in aerobic power and systolic blood pressure. Secondary aims include evaluating the effects of exercise dose on fasting blood lipids and lipoproteins, glucose, insulin, anthropometry, self-reported quality of life, and cardiovascular risk as determined by a multiple logistic risk function. Covariates to be controlled included dietary intake, physical activity (outside of the exercise program), smoking, alcohol intake, sleep habits, medication use (including hormone replacement therapy), demographics, menstrual history, personal and family medical history.

Study Design

Study Type:
Observational
Actual Enrollment :
464 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Dose-response to Exercise in Women Aged 45-75 Years (DREW)
Study Start Date :
Jan 1, 2001
Actual Primary Completion Date :
Dec 1, 2006
Actual Study Completion Date :
Dec 1, 2006

Arms and Interventions

Arm Intervention/Treatment
Non-Exercise Control Group

We randomly assigned 102 women in the non-exercise control group and were asked to maintain their level of activity for the 6-month study period.

Behavioral: Exercise
Compared the effect of 50%, 100%, and 150% of the NIH Consensus Development Panel recommended physical activity dose on fitness in women.

4-kcal/kg Energy Expenditure per week

We randomly assigned 155 women to the 4-kcal/kg per week group for 6 months.

Behavioral: Exercise
Compared the effect of 50%, 100%, and 150% of the NIH Consensus Development Panel recommended physical activity dose on fitness in women.

8-kcal/kg Energy Expenditure per week

We randomly assigned 104 women to the 8-kcal/kg per week group for 6 months.

Behavioral: Exercise
Compared the effect of 50%, 100%, and 150% of the NIH Consensus Development Panel recommended physical activity dose on fitness in women.

12-kcal/kg Energy Expenditure per week

We randomly assigned 103 women to the 12-kcal/kg per week group for 6 months.

Behavioral: Exercise
Compared the effect of 50%, 100%, and 150% of the NIH Consensus Development Panel recommended physical activity dose on fitness in women.

Outcome Measures

Primary Outcome Measures

  1. VO2max and resting systolic blood pressure [at 6 months]

Secondary Outcome Measures

  1. Fasting blood lipids and lipoproteins (total, HDL-, and LDL-cholesterol, triglycerides [at 6 months]

  2. High sensitive C-reactive protein [at 6 months]

  3. Fasting glucose [at 6 months]

  4. Anthropometry (body composition and regional fat distribution) [at 6 months]

  5. Blood pressure response to exercise [at 6 months]

  6. Heart rate variability [at 6 months]

  7. Health-related quality of life and other psychosocial variables [at 6 months]

  8. Cardiovascular disease risk determined by a multiple logistic risk function [at 6 months]

  9. Tertiary Outcomes [at 6 months]

    Other variables of interest include dietary habits, physical activity history, smoking, alcohol intake, sleep habits, medication use (including HRT), demographic characteristics, unstructured physical activity, menstrual history, and personal and family medical history.

Eligibility Criteria

Criteria

Ages Eligible for Study:
45 Years to 75 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No

Postmenopausal women aged 45 to 75 years who are overweight or obese (body mass index of 25 to 40 kg/m2) and have normal or mildly elevated BP.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Oak Cliff-South Dallas Dallas Texas United States 75201
2 The Cooper Institute Dallas Texas United States 75230

Sponsors and Collaborators

  • Pennington Biomedical Research Center
  • National Heart, Lung, and Blood Institute (NHLBI)

Investigators

  • Principal Investigator: Steven N. Blair, PED, University of South Carolina
  • Principal Investigator: Timothy S. Church, MD, PhD, MPH, Pennnington Biomedical Research Center
  • Study Director: Conrad P. Earnest, PhD, University of Bath
  • Study Director: James S. Skinner, hD, Indiana University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Timothy Church, Principal Investigator, Pennington Biomedical Research Center
ClinicalTrials.gov Identifier:
NCT00011193
Other Study ID Numbers:
  • HL66262
  • R01HL066262
First Posted:
Feb 13, 2001
Last Update Posted:
May 28, 2012
Last Verified:
May 1, 2012
Keywords provided by Timothy Church, Principal Investigator, Pennington Biomedical Research Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 28, 2012