The Enabling Reduction of Low-Grade Inflammation in Seniors (ENRGISE) Pilot Study: Screening Methods and Recruitment Results

Author:

Cauley Jane A1,Manini Todd M2,Lovato Laura3,Talton Jennifer3,Anton Steven D2,Domanchuk Kathryn4,Kennedy Kimberly3,Stowe Cynthia L3,Walkup Michael3,Fielding Roger A5,Kritchevsky Stephen B3,McDermott Mary M4,Newman Anne B1,Ambrosius Walter T3,Pahor Marco2,

Affiliation:

1. Department of Epidemiology, Graduate School of Public Health, University of Pittsburgh, Pennsylvania

2. Department of Aging and Geriatric Research, University of Florida, Gainesville

3. Department of Radiology, Wake Forest School of Medicine, Winston-Salem, North Carolina

4. Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois

5. Nutrition, Exercise Physiology and Sarcopenia Laboratory, Jean Mayer Human Nutrition Research Center on Aging, Tufts University, Boston, Massachusetts

Abstract

Abstract Background The Enabling Reduction of Low-grade Inflammation in Seniors (ENRGISE) Pilot Study is a multicenter randomized clinical trial examining the feasibility of testing whether omega-3 fish oil (ω-3) and the angiotensin receptor blocker losartan alone or in combination can reduce inflammation and improve walking speed in older adults with mobility impairment. We describe recruitment methods and results. Methods Eligible participants were 70 years and older, had elevated interleukin-6 levels (2.5–30 pg/mL) and mobility impairment. Results Of those who responded to recruitment, 83% responded to mailings. A total of 5,424 telephone screens were completed; of these, 2,011 (37.1%) were eligible for further screening. The most common reasons for ineligibility at the telephone screens were lack of mobility impairment or use of angiotensin receptor blockers or angiotensin-converting enzyme inhibitors (n=1.789). Of the 1,305 initial screening visits, 1,087 participants had slow gait speed (<1 m/s). Of these, 701 (64%) had elevated interleukin-6 and were eligible for second screening visits. Of the 582 second screening visits, 335 (57.6%) were eligible to be randomized. A total of 289 participants (96% of goal) were randomized: 180 in the ω-3 stratum (240% of goal); 43 in the losartan (57% of goal), and 66 in the combination (44% of goal). The telephone screen and first screening visit to randomization ratio was 19 to 1 and 4.5 to 1, respectively. The estimated cost of recruitment per randomized participant was $1,782. Conclusion Recruitment for ω-3 exceeded goals, but goals for the losartan and combination strata were not met due to the high proportion of participants taking angiotensin receptor blockers or angiotensin-converting enzyme inhibitors.

Funder

National Institutes of Health

National Institute on Aging

Claude D. Pepper Older Americans Independence Centers at the University of Florida

Wake Forest University

Tufts University

University of Pittsburgh

Boston Rehabilitation Outcomes Center

U.S. Department of Agriculture

Publisher

Oxford University Press (OUP)

Subject

Geriatrics and Gerontology,Aging

Reference14 articles.

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