TY - JOUR
T1 - The AgingPLUS trial
T2 - Design of a randomized controlled trial to increase physical activity in middle-aged and older adults
AU - Diehl, Manfred
AU - Nehrkorn-Bailey, Abigail
AU - Thompson, Katherine
AU - Rodriguez, Diana
AU - Li, Kaigang
AU - Rebok, George W.
AU - Roth, David L.
AU - Chung, Shang En
AU - Bland, Christina
AU - Feltner, Skylar
AU - Forsyth, Garrett
AU - Hulett, Nicholas
AU - Klein, Berkeley
AU - Mars, Paloma
AU - Martinez, Karla
AU - Mast, Sarah
AU - Monasterio, Rachel
AU - Moore, Kristen
AU - Schoenberg, Hayden
AU - Thomson, Elizabeth
AU - Tseng, Han Yun
N1 - Funding Information:
Support for this study is provided by grant R01 AG051723 from the National Institute on Aging , National Institutes of Health (NIA/NIH). Funding for the development of Aging PLUS and the pilot work was provided by small grants from the Colorado School of Public Health at Colorado State University and the Colorado Clinical and Translational Sciences Institute (CCTSI), supported by NIH grant UL1 TR002535 .
Funding Information:
The Aging PLUS trial is funded by the National Institute on Aging (R01 AG051723), National Institutes of Health. Pilot work that generated the preliminary data for the application to the National Institute on Aging was funded by a faculty seed grant from the Colorado School of Public Health at Colorado State University and a pilot grant from the Colorado Clinical and Translaitonal Sciences Institute (UL1 TR002535; National Center for Advancing Translational Sciences, National Institutes of Health). The Institutional Review Board (IRB) of Colorado State University approved all components of the study, and the trial is registered with ClinicalTrials.gov ( NCT03299348 ). All study procedures adhere to the Consolidated Standards of Reporting Trials (CONSORT; [ 68 ]) guidelines to assure the scientific rigor of the trial and the reproducibility of the protocol and the anticipated findings.
Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2020/9
Y1 - 2020/9
N2 - Background: Negative views of aging (NVOA), low self-efficacy beliefs, and poor goal planning skills represent risk factors that undermine adults' motivation to engage in physical activity (PA). Targeting these three risk factors may motivate adults to become physically active. Objective: To assess the efficacy of AgingPLUS, a 4-week educational program that explicitly targets NVOA, low self-efficacy beliefs, and poor goal planning skills compared to a 4-week health education program. The study also examines the role of NVOA, self-efficacy beliefs, and goal planning as the mechanisms underlying change in PA. Design: This randomized controlled trial (RCT) utilizes the experimental medicine approach to assess change in PA as a function of modifying three risk factors. The RCT recruitment target includes 288 mostly sedentary adults ranging in age from 45 to 75 years. Methods: Eligible middle-aged and older adults are recruited through community sources. Participants are randomized to either the AgingPLUS or the control group. Participants in both groups are enrolled in the trial for 8 months total, with four assessment points: Baseline (pre-test), Week 4 (immediate post-test), Week 8 (delayed post-test), and Month 6 (long-term follow-up). The intervention takes place over 4 consecutive weeks with 2-h sessions each week. PA engagement is the primary outcome variable. Positive changes in NVOA, self-efficacy beliefs, and goal planning are the intervention targets and hypothesized mediators of increases in PA. By utilizing a multi-component approach and targeting a cluster of psychological mechanisms, the AgingPLUS program implements the experimental medicine approach to health behavior change.
AB - Background: Negative views of aging (NVOA), low self-efficacy beliefs, and poor goal planning skills represent risk factors that undermine adults' motivation to engage in physical activity (PA). Targeting these three risk factors may motivate adults to become physically active. Objective: To assess the efficacy of AgingPLUS, a 4-week educational program that explicitly targets NVOA, low self-efficacy beliefs, and poor goal planning skills compared to a 4-week health education program. The study also examines the role of NVOA, self-efficacy beliefs, and goal planning as the mechanisms underlying change in PA. Design: This randomized controlled trial (RCT) utilizes the experimental medicine approach to assess change in PA as a function of modifying three risk factors. The RCT recruitment target includes 288 mostly sedentary adults ranging in age from 45 to 75 years. Methods: Eligible middle-aged and older adults are recruited through community sources. Participants are randomized to either the AgingPLUS or the control group. Participants in both groups are enrolled in the trial for 8 months total, with four assessment points: Baseline (pre-test), Week 4 (immediate post-test), Week 8 (delayed post-test), and Month 6 (long-term follow-up). The intervention takes place over 4 consecutive weeks with 2-h sessions each week. PA engagement is the primary outcome variable. Positive changes in NVOA, self-efficacy beliefs, and goal planning are the intervention targets and hypothesized mediators of increases in PA. By utilizing a multi-component approach and targeting a cluster of psychological mechanisms, the AgingPLUS program implements the experimental medicine approach to health behavior change.
KW - Adulthood
KW - Goal planning
KW - Health behavior change
KW - Negative views of aging
KW - Physical activity
KW - Self-efficacy beliefs
UR - http://www.scopus.com/inward/record.url?scp=85089352911&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85089352911&partnerID=8YFLogxK
U2 - 10.1016/j.cct.2020.106105
DO - 10.1016/j.cct.2020.106105
M3 - Article
C2 - 32791322
AN - SCOPUS:85089352911
SN - 1551-7144
VL - 96
JO - Contemporary Clinical Trials
JF - Contemporary Clinical Trials
M1 - 106105
ER -